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This project was developed by a former Engineer and now a patent agent assistant studding towards LLM degree. Seeing new inventions is very interesting to me. I created this site to outlines my favorite inventions along with inventions that I believe have potential.

Triazinyl-sulfonyl-ureas and isoureas

by Levitt, George;



BACKGROUND OF THE INVENTION

This invention relates to ureas and isoureas and in particular their use as agricultural chemicals and particularly as herbicides.

U.S. Pat. No. 4,127,405 teaches compounds which are useful for controlling weeds in wheat having the formula ##STR1## wherein ##STR2##

R.sub.3 and R.sub.6 are independently hydrogen, fluorine, chlorine, bromine, iodine, alkyl of 1-4 carbon atoms, alkoxy of 1-4 carbon atoms, nitro, trifluoromethyl, cyano, CH.sub.3 S(O).sub.n --or CH.sub.3 CH.sub.2 S(O).sub.n --;

R.sub.4 is hydrogen, fluorine, chlorine, bromine or methyl;

R.sub.5 is hydrogen, fluorine, chlorine, bromine, methyl or methoxy;

R.sub.7 is hydrogen, fluroine, chlorine, bromine, alkyl of 1-2 carbon atoms or alkoxy of 1--2 carbon atoms;

R.sub.8 is hydrogen, methyl, chlorine or bromine;

R.sub.9 and R.sub.10 are independently hydrogen, methyl, chlorine or bromine;

W and Q are independently oxygen or sulfur; n is 0, 1 or 2;

X is hydrogen, chlorine, bromine, methyl, ethyl, alkoxy of 1--3 carbon atoms, trifluoromethyl, CH.sub.3 S--or CH.sub.3 OCH.sub.2 -; and

Y is methyl or methoxy; or their agriculturally suitable salts; provided that:

(a) when R.sub.5 is other than hydrogen, at least one of R.sub.3, R.sub.4, R.sub.6 and R.sub.7 is other than hydrogen and at least two of R.sub.3, R.sub.4, R.sub.6 and R.sub.7 must be hydrogen;

(b) when R.sub.5 is hydrogen and all of R.sub.3, R.sub.4, R.sub.6 and R.sub.7 are other than hydrogen, then all of R.sub.3, R.sub.4, R.sub.6 and R.sub.7 must be either chlorine or methyl; and

(c) when R.sub.3 and R.sub.7 are both hydrogen, at least one of R.sub.4, R.sub.5 or R.sub.6 must be hydrogen.

French Pat. No. 1,468,747 discloses the following para-substituted phenylsulfonamides, useful as antidiabetic agents: ##STR3## wherein R.dbd.H, halogen, CF.sub.3 or alkyl.

Logemann et al. Chem. Ab., 53, 18052 g (1959), disclose a number of sulfonamides, including uracil derivatives and those having the formula: ##STR4## wherein R is butyl, phenyl or and R.sub.1 is hydrogen or methyl. When tested for hypoglycemic effect in rats (oral doses of 25 mg/100 g), the compounds in which R is butyl and phenyl were most potent. The others were of low potency or inactive.

Wojciechowski, J. Acta. Polon. Pharm. 19, p. 121-5 (1962) [Chem Ab., 59 1633 e] describes the synthesis of N-[(2,6-dimethoxypyrimidin-4-yl)aminocarbonyl]-4methylbenzenesulfonamide: ##STR5## Based upon similarity to a known compound, the author predicted hypoglycemic activity for the foregoing compound.

Netherlands Pat. No. 121,788, published Sept. 15, 1966, teaches the preparation of compounds of Formula (i), and their use as general or selective herbicides, ##STR6## wherein

R.sub.1 and R.sub.2 may independently be alkyl of 1-4 carbon atoms; and

R.sub.3 and R.sub.4 may independently be hydrogen, chlorine or alkyl of 1-4 carbon atoms.

Compounds of Formula (ii), and their use as antidiabetic agents, are reported in J. Drug. Res. 6, 123 (1974), ##STR7## wherein R is pyridyl.

The presence of undesired vegetation causes substantial damage to useful crops, especially agricultural products that satisfy man's basic food needs, such as soybeans, barley, wheat, and the like. The current population explosion and concomitant world food shortage demand improvements in the efficiency of producing these crops. Prevention or minimizing the loss of a portion of such valuable crops by killing, or inhibiting the growth of undesired vegetation is one way of improving this efficiency.

A wide variety of materials useful for killing, or inhibiting (controlling) the growth of undesired vegetation is available; such materials are commonly referred to as herbicides. The need exists, however, for still more effective herbicides that destroy or retard weeds without causing significant damage to useful crops.

SUMMARY OF THE INVENTION

This invention relates to novel compounds of Formulas I, II, and III and their agriculturally suitable salts, suitable agricultural compositions containing them, and methods of using them as selective, as well as general herbicides having both pre-emergence and post-emergence activity. Some of the compounds are especially useful for controlling weeds in crops such as soybeans: ##STR8## wherein

W' is O or S;

A' is H, Cl, Br, C.sub.1 -C.sub.4 alkyl, OCH.sub.3, NO.sub.2 or CF.sub.3 ; ##STR9## where

R.sup.III is H, C.sub.1 -C.sub.4 alkyl or C.sub.3 C.sub.4 alkenyl; when Q is O or S then

R.sup.I is C.sub.1 -C.sub.6 alkyl; C.sub.3 C.sub.6 alkenyl; C.sub.3 -C.sub.6 alkynyl; C.sub.2 -C.sub.6 alkyl substituted with 1-3Cl, F or Br, or one of CN or OCH.sub.3 ; C.sub.3 -C.sub.6 alkenyl substituted with 1-3 Cl; C.sub.3 -C.sub.6 alkynyl substituted with Cl; C.sub.5 -C.sub.6 cycloalkyl; cyclohexenyl; cyclohexyl substituted with 1-3 CH.sub.3 ; C.sub.4 -C.sub.7 cycloalkylalkyl or ##STR10## where R.sub.7 and R.sub.8 are independently H, Cl, CH.sub.3 or OCH.sub.3 ;

n is 0 or 1; and

R.sub.9 is H or CH.sub.3 ;

when Q is O then R.sup.I is ##STR11## CH.sub.2 OR.sub.6 '; where R.sub.6 ' is C.sub.1 -C.sub.4 alkyl; provided R.sup.I has a total of .ltoreq.13 carbon atoms; when Q is ##STR12## then

R.sup.I is H; C.sub.1 -C.sub.6 alkyl; -CH.sub.2 CH.sub.2 OR.sub.10 ; -CH.sub.2 CH.sub.2 CH.sub.2 OR.sub.10 ; where R.sub.10 is CH.sub.3, CH.sub.3 CH.sub.2, CH(CH.sub.3).sub.2, or phenyl; C.sub.3 -C.sub.6 alkenyl; C.sub.3 -C.sub.6 cycloalkyl; C.sub.5 -C.sub.6 cycloalkenyl; C.sub.6 cycloalkyl substituted with any one of 1-2 OCH.sub.3, 1-3 CH.sub.3, -CH.sub.2 CH.sub.3 or CH.sub.3 ; C.sub.4 -C.sub.7 cycloalkylalkyl; --CH.sub.2 CN; --CH.sub.2 CH.sub.2 CN; ##STR13## where

R' is H, C.sub.1 -C.sub.4 alkyl, OCH.sub.3, F, Cl, Br, CN, NO.sub.2 or CF.sub.3 ;

R" is H, CH.sub.3, Cl, F or Br;

R.sub.7, R.sub.8 and R.sub.9 are as previously defined; R.sub.6 is H, C.sub.1 -C.sub.3 alkyl; CH.sub.2 CN; CH.sub.2 CH.sub.2 --CN or --CH.sub.2 --CH.dbd.CH.sub.2 and R.sub.6 and R.sup.I may be taken together to form--(CH.sub.2).sub.4 --, --(CH.sub.2).sub.5 --or --CH.sub.2 CH.sub.2 O--CH.sub.2 CH.sub.2 --; with the proviso that when R.sub.6 is CH.sub.2 CH.sub.2 CN or CH.sub.2 CN, then R.sup.I is CH.sub.2 CH.sub.2 CN or CH.sub.2 CN; and R.sup.I and R.sub.6 have a total carbon atom cound of .ltoreq.13; and when R.sup.I is OCH.sub.3 or OCH.sub.2 CH.sub.3 then R.sub.6 is CH.sub.3 or H; when A is ##STR14## then

R.sup.II is H, C.sub.1 -C.sub.6 alkyl; C.sub.3 -C.sub.6 alkenyl; phenyl; benzyl; benzyl or phenyl substituted with 1--2 Cl, 1--2 OCH.sub.3, 1--2 CH.sub.3 ; C.sub.5 -C.sub.6 cycloalkyl; C.sub.4 --C.sub.7 cycloalkylalkyl with the proviso that when T is .dbd.N--OR.sup.III, then R.sup.II must be C.sub.1 --C.sub.6 alkyl or Ch.sub.3 --C.sub.6 alkenyl; B is ##STR15## where

R.sub.4 is H or CH.sub.3 ; W is O or S;

R.sub.5 is H, or CH.sub.3 ; with the proviso that either R.sub.4 or R.sub.5 must be H;

R.sup.IV is C.sub.1 --C.sub.6 alkyl or C.sub.3 --C.sub.4 alkenyl; ##STR16## where Z is N, CH or C-F;

X.dbd.H, Cl, --CH.sub.3, --OCH.sub.3 or --OCH.sub.2 CH.sub.3 ;

Y.dbd.H; Cl; c.sub.1 --C.sub.4 alkyl substituted with ##STR17## C.sub.3 --C.sub.4 akenyl; --O--(CH.sub.2).sub.n' O-(C.sub.1 --C.sub.3 alkyl) where n' is 2 or 3; ##STR18## --N(C.sub.1 --C.sub.4 alkyl).sub.2 or C.sub.1 --C.sub.6 alkoxy; SCN; --N.sub.3 ; NR.sub.11 R.sub.12 where R.sub.11 is H or CH.sub.3 and R.sub.12 is H, --OCH.sub.3, C.sub.1 --C.sub.4 alkyl, C.sub.3 --C.sub.6 cycloalkyl, C.sub.3 --C.sub.4 akenyl, C.sub.2 --C.sub.3 alkyl substituted with OCH.sub.3 or OC.sub.2 H.sub.5, C.sub.1 --C.sub.2 alkyl substituted with --CN, CO.sub.2 H, CO.sub.2 CH.sub.3 or CO.sub.2 C.sub.2 H.sub.5, and R.sub.11 and R.sub.12 can be taken together to form --CH.sub.2 CH.sub.2 CH.sub.2 CH.sub.2 --or CH.sub.2 CH.sub.2 OCH.sub.2 CH.sub.2 --; --O--R.sub.9 where R.sub.9 is C.sub.1 --C.sub.4 alkyl, C.sub.2 --C.sub.4 alkyl substituted with 1--3 atoms of F, Cl or Br, C.sub.1 --C.sub.2 alkyl substituted with cyano, C.sub.3 -- C.sub.4 alkenyl, --CH.sub.2 C.tbd.CR.sub.13, ##STR19## R.sub.13 is H, CH.sub.3 or CH.sub.2 Cl; SR.sub.14 ; where R.sub.14 is C.sub.1 --C.sub.4 alkyl, allyl, propargyl or C.sub.1 --C.sub.2 alkyl substituted with CN; with the proviso that when X and Y are both H, then

R.sup.I and R.sup.II are less than 5 carbons;

X.sub.1 .dbd.H, Cl, OCH.sub.3, OCH.sub.2 CH.sub.3 or CH.sub.3 ;

Y.sub.1 .dbd.H, OCH.sub.3 or CH.sub.3 ; and

X.sub.II .dbd.O or CH.sub.2 and further provided that when A contains greater than 5 carbon atoms, then Y must contain .ltoreq.4 carbon atoms,

and their agriculturally suitable salts.

Preferred Compounds

Preferred for reasons of higher activity and/or lower cost and/or greater ease of synthesis are compounds:

(1) Of the Generic scope in which B is ##STR20##

More Preferred and in increasing order for reasons of higher activity and/or even lower cost and/or even greater ease of synthesis are compounds:

(2) Preferred (1) in which W' is sulfur;

(2a) More Preferred (2) in which T is oxygen;

(3) More Preferred (2a) in which R.sub.1 is ##STR21##

(4) More Preferred (3) where Q is O or S and R.sub.I is C.sub.1 --C.sub.4 alkyl; C.sub.3 --C.sub.4 alkenyl; c.sub.3 --C.sub.4 alkynyl; C.sub.2 --C.sub.3 alkyl substituted with CN, OCH.sub.3 or 1--3 F, Cl or Br; C.sub.3 --C.sub.4 alkenyl substituted with 1--3 Cl; C.sub.3 --C.sub.4 alkynyl substituted with Cl;

(5) More Preferred (3) in which O is oxygen and R.sup.I is CH.sub.2 CH.sub.2 OR.sub.15 ; CH.sub.2 Ch.sub.2 CH.sub.2 OR.sub.15 ; ##STR22## where R.sub.6.sup.' is CH.sub.3 or CH.sub.3 CH.sub.2 ; ##STR23##

(6) More Preferred (3) in which O is ##STR24## and R.sup.I is H, C.sub.1 -C.sub.4 alkyl, CH.sub.2 CH.sub.2 OR.sub.10, CH.sub.2 CH.sub.2 CH.sub.2 OR.sub.10 where R.sub.10 is CH.sub.3 or CH.sub.3 CH.sub.2 ; C.sub.3 -C.sub.4 alkenyl; CH.sub.2 CN; CH.sub.2 CH.sub.2 CN; OCH.sub.3 or OCH.sub.2 CH.sub.3 ; R.sup.6 is H, C.sub.1 -C.sub.2 alkyl, CH.sub.2 CN or CH.sub.2 CH.sub.2 CN and R.sub.6 and R.sup.I can be taken together to form (CH.sub.2).sub.4.

(7) More Preferred (3) in which R.sup.II is H or C.sub.1 -C.sub.3 alkyl;

(8) More Preferred (4), (5), (6), and (7) in which

Z is CH or N;

X is CH.sub.3 or CH.sub.3 O; and

Y is C.sub.1 -C.sub.2 alkyl; C.sub.1 -C.sub.2 alkyl substituted with OCH.sub.3 ; OCH.sub.2 CH.sub.3, CN or 1-3 atoms of F, Cl or Br; ##STR25## where L is NH.sub.2, OH, ##STR26## N(CH.sub.3).sub.2, NHCH.sub.3, C.sub.1 -C.sub.2 alkoxy; SCN; N.sub.3 ; NR.sub.11 R.sub.12 where R.sub.11 is H or CH.sub.3 ; R.sub.12 is H, CH.sub.3, CH.sub.3 CH.sub.2, OCH.sub.3 ; OR.sub.9 where R.sub.9 is CH.sub.3, CH.sub.3 CH.sub.2 ; CH.sub.2 CH.dbd.CH.sub.2 or CH.sub.2 C.tbd.CH; R.sub.9 is also C.sub.2 alkyl substituted with 1-3 F, Cl or Br; CH.sub.3 S;

(9) More Preferred (3) in which A' is H, Cl or Br;

(10) More Preferred (9) in which Q is O or S and R.sup.I is C.sub.1 -C.sub.4 alkyl, CH.sub.2 CH.dbd.CH.sub.2 or CH.sub.2 CH.sub.2 Cl;

(11) More Preferred (9) in which Q is O and R.sup.I is CH.sub.2 CH.sub.2 OCH.sub.3, ##STR27##

(12) More Preferred (9) in which Q is ##STR28## and R.sup.I is H, C.sub.1 -C.sub.3 alkyl, OCH.sub.3 or OCH.sub.2 CH.sub.3 and R.sub.6 is H or C.sub.1 -C.sub.2 alkyl;

(13) More Preferred (9) in which R.sup.II is H or CH.sub.3 ;

(14) More Preferred (10), (11), (12) and (13) in which A' is H; Y is CH.sub.3, OCH.sub.3, OCH.sub.2 CH.sub.3, OCH.sub.2 CF.sub.3, OCH.sub.2 CH.dbd.CH.sub.2 or OCH.sub.2 C.tbd.CH;

(15) More Preferred (8) in which A is ##STR29## and Q is oxygen or sulfur and R.sup.I is Ch.sub.3 or CH.sub.2 CH.sub.3 ; Q is ##STR30## and R.sup.I is H, CH.sub.3 or OCH.sub.3 and R.sub.6 is CH.sub.3 ; R.sub.1 is ##STR31## and Y is CH.sub.3 or OCH.sub.3 ;

(16) More Preferred (15) of Formula I;

(17) More Preferred (15) of Formula II;

(18) More Preferred (15) of Formula III.

Equally More Preferred in increasing order and for reasons of higher activity and/or even lower cost and/or even greater ease of synthesis are:

(19) Compounds of Preferred (1) in which W' is oxygen;

(20) Compounds of More Preferred (19) in which T is oxygen;

(21) More Preferred (20) in which R.sub.1 is ##STR32##

(22) More Preferred (21) where Q is O or S and R.sub.1 is C.sub.1 -C.sub.4 alkyl; C.sub.3 -C.sub.4 alkenyl; C.sub.3 -C.sub.4 alkynyl; C.sub.2 -C.sub.3 alkyl substituted with CN, OCH.sub.3 or 1-3 F, Cl or Br; C.sub.3 -C.sub.4 alkenyl substituted with 1-3 Cl; C.sub.3 -C.sub.4 alkynyl substituted with Cl;

(23) More Preferred (21) in which Q is oxygen and R.sup.I is Ch.sub.2 CH.sub.2 OR.sub.15 ; CH.sub.2 CH.sub.2 CH.sub.2 OR.sub.15 ; ##STR33## where R.sub.15 is CH.sub.2 CH.sub.3 ; CH.sub.2 CN; CH.sub.2 OR.sub.6.sup.' where R.sub.6 .sup.' is CH.sub.3 or CH.sub.3 CH.sub.2 ; ##STR34##

(24) More Preferred (21) in which Q is ##STR35## and R.sup.I is H, C.sub.1 -C.sub.4 alkyl, CH.sub.2 CH.sub.2 OR.sub.10, CH.sub.2 CH.sub.2 CH.sub.2 OR.sub.10 where R.sub.10 is CH.sub.3 or CH.sub.3 CH.sub.2 ; C.sub.3 -C.sub.4 alkenyl; CH.sub.2 CN; CH.sub.2 CH.sub.2 CN; OCH.sub.3 or OCH.sub.2 CH.sub.3 ; R.sup.6 is H, C.sub.1 -C.sub.2 alkyl, CH.sub.2 CN or CH.sub.2 CH.sub.2 CN and R.sub.6 and R.sup.I can be taken together to form (CH.sub.2).sub.4.

(25) More Preferred (21) in which R.sup.II is H or C.sub.1 -C.sub.3 alkyl;

(26) More Preferred (22), (23), (24) and (25) in which Z is CH or N; X is CH.sub.3 or CH.sub.3 O; and Y is C.sub.1 -C.sub.2 alkyl; C.sub.1 -C.sub.2 alkyl substituted with OCH.sub.3 ; OCH.sub.2 CH.sub.3, CN or 1-3 atoms of F, Cl or Br; ##STR36## where L is NH.sub.2, OH, ##STR37## N(CH.sub.3).sub.2, NHCH.sub.3, C.sub.1 -C.sub.2 alkoxy; SCN; N.sub.3 ; NR.sub.11 R.sub.12 where R.sub.11 is H or CH.sub.3 ; R.sub.12 is H, CH.sub.3, CH.sub.3 CH.sub.2, OCH.sub.3 ; OR.sub.9 wherein R.sub.9 is CH.sub.3, CH.sub.3 CH.sub.2, CH.sub.2 CH.dbd.CH.sub.2 or CH.sub.2 C.tbd.CH; R.sub.9 is also C.sub.2 alkyl substituted with 1-3 F, Cl or Br; CH.sub.3 S;

(27) Preferred (21) in which A' is H, Cl or Br;

(28) More Preferred (27) in which Q is O or S and R.sup.I is C.sub.1 -C.sub.4 alkyl, CH.sub.2 CH.dbd.CH.sub.2 or Ch.sub.2 CH.sub.2 Cl;

(29) More Preferred (27) in which Q is O and R.sup.I is CH.sub.2 CH.sub.2 OCH.sub.3, ##STR38##

(30) More Preferred (27) in which Q is ##STR39## and R.sup.I is H, C.sub.1 -C.sub.3 alkyl, OCH.sub.3 or OCH.sub.2 CH.sub.3 and R.sub.6 is H or C.sub.1 -C.sub.2 alkyl;

(31) More Preferred (27) in which R.sup.II is H or CH.sub.3 ;

(32) More Preferred (28), (29), (30) and (31) in which A' is H; Y is CH.sub.3, OCH.sub.3, OCH.sub.2 CH.sub.3, OCH.sub.2 CF.sub.3, OCH.sub.2 CH.dbd.CH.sub.2 or OCH.sub.2 CH.tbd.CH;

(33) More Preferred (27) in which A is ##STR40## and Q is oxygen or sulfur and R.sup.I is CH.sub.3 or CH.sub.2 CH.sub.3 ; Q is ##STR41## and R.sup.I is H, CH.sub.3 or OCH.sub.3 and R.sub.6 is CH.sub.3 ; R.sub.1 is ##STR42## and Y is CH.sub.3 or OCH.sub.3 ;

(34) More Preferred (33) of Formula I;

(35) More Preferred (33) of Formula II;

(36) More Preferred (33) of Formula III.

Specifically Preferred for reasons of highest activity and/or lowest cost and/or greatest ease of synthesis are:

methyl 3-[[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]-aminosulfonyl]-2-thiophene carboxylate

methyl 3-[[(4,6-dimethylpyrimidin-2-yl)aminocarbonyl]-aminosulfonyl]-2-thiophenec arboxylate

methyl 3-[[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]-aminosulfonyl]-2-thio phenecarboxylate

methyl 3-[[(4,6-dimethoxy-1,3,5-triazin-2-yl)aminocarbonyl]-aminosulfonyl]-2-thio phenecarboxylate

methyl 3-[[(4,6-dimethyl-1,3,5-triazin-2-yl)aminocarbonyl]-aminosulfonyl]-2-thiop henecarboxylate

methyl 3-[[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)-aminocarbonyl]aminosulfonyl]-2 -thiophenecarboxylate

methyl 3-[[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]aminosulfonyl]-2-furancarbo xylate

methyl 3-[[(4,6-dimethylpyrimidin-2-yl)aminocarbonyl]-aminosulfonyl]-2-furancarbo xylate

methyl 3-[[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]-aminosulfonyl]-2-fura ncarboxylate

methyl 3-[[(4,6-dimethoxy-1,3,5-triazin-2-yl)aminocarbonyl]-aminosulfonyl]-2-fura ncarboxylate

methyl 3-[[(4,6-dimethyl-1,3,5-triazin-2-yl)aminocarbonyl]-aminosulfonyl]-2-furan carboxylate

methyl 3-[[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)-aminocarbonyl]aminosulfonyl]-2 -furancarboxylate

methyl 2-[[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]-aminosulfonyl]-3-thiophene carboxylate

methyl 2-[[(4,6-dimethylpyrimidin-2-yl)aminocarbonyl]-aminosulfonyl]-3-thiophenec arboxylate

methyl 2-[[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]-aminosulfonyl]-3-thio phenecarboxylate

methyl 2-[[(4,6-dimethoxy-1,3,5-triazin-2-yl)aminocarbonyl]-aminosulfonyl]-3-thio phenecarboxylate

methyl 2-[[(4,6-dimethyl-1,3,5-triazin-2-yl)aminocarbonyl]-aminosulfonyl]-3-thiop henecarboxylate

methyl 2-[[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)-aminocarbonyl]aminosulfonyl]-3 -thiophenecarboxylate

methyl 2-[[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]-aminosulfonyl]-3-furancarb oxylate

methyl 2-[[(4,6-dimethylpyrimidin-2-yl)aminocarbonyl]-aminosulfonyl]-3-furancarbo xylate

methyl 2-[[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]aminosulfonyl]-3-furan carboxylate

methyl 2-[[(4,6-dimethoxy-1,3,5-triazin-2-yl)aminocarbonyl]aminosulfonyl]-3-furan carboxylate

methyl 2-[[(4,6-dimethyl-1,3,5-triazin-2-yl)aminocarbonyl]aminosulfonyl]-3-furanc arboxylate

methyl 2-[[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)aminocarbonyl]aminosulfonyl]-3- furancarboxylate

N-[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]-2-(1-pyrrolidinylcarbon yl)-3-thiophenesulfonamide

1-methylethyl 3-[[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]-aminosulfonyl]-2-thiophene carboxylate

2-propenyl 3-[[(4-methoxy-6-methylpyrimidin-2-yl)-aminocarbonyl]aminosulfonyl]-2-thio phenecarboxylate

1-methylethyl 3-[[(4-methoxy-6-methylpyrimidin-2-yl)-aminocarbonyl]aminosulfonyl]-2-thio phenecarboxylate.

Novel Intermediates

Also novel and useful for the preparation of compounds of Formulas I, II and III are compounds of Formulas I', II' and III'. ##STR43## wherein

R.sup.I is H or M;

M is a cation of an alkalii metal or of a tertiary amine of up to 12 carbon atoms;

A', W', B, are as previously defined.

Preferred and in increasing order for reasons of lower cost and/or greater ease of synthesis and/or higher activity of derived compounds are those intermediate

(1) Compounds of formulas I', II' and III' in which W' is sulfur, B is SO.sub.2 NHCONHR.sub.1, A' is H, Cl or Br and R.sub.1 is ##STR44##

(2) Compounds of Preferred (1) in which X is CH.sub.3 or OCH.sub.3 ; Y is CH.sub.3, OCH.sub.3, OCH.sub.2 CH.sub.3, OCH.sub.2 CF.sub.3, OCH.sub.2 CH.dbd.CH.sub.2 or OCH.sub.2 --C.tbd.C-H; Z is CH or N;

(3) Compounds of Preferred 2) in which Y is CH.sub.3 or OCH.sub.3 ; ##STR45## A' is H;

(4) Compounds of Preferred (3) of Formula I';

(5) Conmpounds of Preferred (4) of Formula II';

(6) Compounds of Preferred (5) of Formula III';

Equally Preferred in increasing order, for reasons of lower cost and/or greater ease of synthesis and/or higher activity of derived compound are those intermediate:

(7) Compounds of formulas I', II' and III' in which W' is oxygen; B is SO.sub.2 NHCONHR.sub.1, A' is H, Cl or Br, and ##STR46##

(8) Compounds of Preferred (7) in which X is CH.sub.3 or OCH.sub.3 ; Y is CH.sub.3, OCH.sub.3, OCH.sub.2 CH.sub.3, OCH.sub.2 CF.sub.3, OCH.sub.2 CH.dbd.CH.sub.2 or OCH.sub.2 C.tbd.C-H; and Z is CH or N;

(9) Compounds of Preferred (8) in which Y is CH.sub.3 or OCH.sub.3 ; ##STR47##

A' is H;

(10) Compounds of Preferred (9) of Formula I',

(11) Compounds of Preferred (9) of Formula II';

(12) Compounds of Preferred (9) of Formula III';

Specifically Preferred for reasons of lowest cost and/or greatest ease of synthesis and/or highest activity or desired compounds are:

3-[[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]aminosulfonyl]-2-thiopheneca rboxylic acid

3-[[(4,6-dimethylpyrimidin-2-yl)aminocarbonyl]aminosulfonyl]-2-thiophenecar boxylic acid

3-[[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]aminosulfonyl]-2-thioph enecarboxylic acid

3-[[(4,6-dimethoxy-1,3,5-triazin-2-yl)aminocarbonyl]aminosulfonyl]-2-thioph enecarboxylic acid

3-[[(4,6-dimethyl-1,3,5-triazin-2-yl)aminocarbonyl]aminosulfonyl]-2-thiophe necarboxylic acid

3-[[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)aminocarbonyl]aminosulfonyl]-2-t hiophenecarboxylic acid

3-[[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]aminosulfonyl]-2-furancarbox ylic acid

3-[[(4,6-dimethylpyrimidin-2-yl)aminocarbonyl]aminosulfonyl]-2-furancarboxy lic acid

3-[[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]aminosulfonyl]-2-furanc arboxylic acid

3-[[(4,6-dimethoxy-1,3,5-triazin-2-yl)aminocarbonyl]aminosulfonyl]-2-furanc arboxylic acid

3-[[(4,6-dimethyl-1,3,5-triazin-2-yl)aminocarbonyl]aminosulfonyl]-2-furanca rboxylic acid

3-[[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)aminocarbonyl]aminosulfonyl]-2-f urancarboxylic acid

2-[[(4,6-dimethoxypyrimidin-2yl)aminocarbonyl]aminosulfonyl]-3-thiophenecar boxylic acid

2-[[(4,6-dimethylpyrimidin-2-yl)aminocarbonyl]aminosulfonyl]-3-thiophenecar boxylic acid

2-[[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]aminosulfonyl]-3-thioph enecarboxylic acid

2-[[(4,6-dimethoxy-1,3,5-triazin-2-yl)aminocarbonyl]aminosulfonyl]-3-thioph enecarboxylic acid 2-[[(4,6-dimethyl-1,3,5-triazin-2-yl)aminocarbonyl]aminosulfonyl]-3-thioph enecarboxylic acid

2-[[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)aminocarbonyl]aminosulfonyl]-3-t hiophenecarboxylic acid

2-[[(4,6-dimethoxypyrimidin-2yl)aminocarbonyl]aminosulfonyl]-3-furancarboxy lic acid

2-[[(4,6-dimethylpyrimidin-2-yl)aminocarbonyl]aminosulfonyl]-3-furancarboxy lic acid

2-[[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]aminosulfonyl]-3-furanc arboxylic acid

2-[[(4,6-dimethoxy-1,3,5-triazin-2-yl)aminocarbonyl]aminosulfonyl]-3-furanc arboxylic acid

2-[[(4,6-dimethyl-1,3,5-triazin-2-yl)aminocarbonyl]aminosulfonyl]-3-furanca rboxylic acid

2-[[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)aminocarbonyl]aminosulfonyl]-3-f urancarboxylic acid

Also novel and useful for the preparation of compounds of Formulas I, II and III are compounds of Formulas I", II" and III" ##STR48## wherein

W is oxygen or sulfur;

W' is oxygen or sulfur;

A' is H, Cl, Br, C.sub.1 -C.sub.4 alkyl, OCH.sub.3, NO.sub.2 or CF.sub.3 ;

R.sup.I is C.sub.1 -C.sub.6 alkyl; C.sub.3 -C.sub.6 alkenyl; C.sub.3 -C.sub.6 alkynyl; C.sub.2 -C.sub.6 alkyl substituted with Cl, CN or OCH.sub.3 ; C.sub.3 -C.sub.6 alkenyl substituted with 1-3 Cl; C.sub.3 -C.sub.6 alkynyl substituted with Cl; C.sub.5 -C.sub.6 cycloalkyl; cyclohexenyl; cyclohexyl substituted with 1-3 CH.sub.3 ; C.sub.4 -C.sub.7 cycloalkylalkyl or ##STR49## where R.sub.7 and R.sub.8 are independently H, Cl, CH.sub.3 or OCH.sub.3 ;

n is 0 or 1; and

R.sub.9 is ##STR50## where R.sub.15 is ##STR51## where R.sub.16 is CH.sub.3, C.sub.2 H.sub.5, CH(CH.sub.3).sub.2, phenyl, CH.sub.2 CH.sub.2 Cl, CH.sub.2 CCl.sub.3, and n' is 2 or 3; ##STR52## where R.sub.6 'is C.sub.1 -C.sub.4 alkyl; provided R.sup.I has a total of .sub..ltoreq. 13 carbon atoms.

Preferred in increasing order for reasons of lower cost and/or greater ease of synthesis and/or higher activity of desired compounds are those intermediate:

(1) Compounds of formulas I", II" and III" in which W' is sulfur; W is oxygen; A' is H, Cl or Br; and R.sup.I is C.sub.1 -C.sub.4 alkyl; ##STR53##

(2) Compounds of Preferred (1) in which R.sup.I is CH.sub.3 or CH.sub.2 CH.sub.3 ; A.sup.I is H;

(3) Compounds of Preferred (2) of Formula I";

(4) Compounds of Preferred (2) of Formula II";

(5) Compounds of Preferred (2) of Formula III".

Equally Preferred in increasing order for reasons of lower cost and/or greater ease of synthesis and/or higher activity of derived compounds are those intermediate:

(6) Compounds of formulas I", II", and III" in which W' is oxygen; W is oxygen; A' is H, Cl or Br;

(7) Compounds of Preferred (6) in which R.sup.I is CH.sub.3 or CH.sub.2 CH.sub.3 ; A.sup.I is H;

(8) Compounds of Preferred (7) of Formula I".

(9) Compounds of Preferred (7) of Formula II".

(10) Compounds of Preferred (7) of Formula III".

Specifically Preferred for reasons of lowest cost and/or greatest ease of synthesis and/or highest activity of desired compounds are:

methyl 3-(isocyanatosulfonyl)-2-thiophenecarboxylate

methyl 2-(isocyanatosulfonyl)-3-thiophenecarboxylate

methyl 4-(isocyanatosulfonyl)-3-thiophenecarboxylate

methyl 3-(isocyanatosulfonyl)-2-furancarboxylate

methyl 2-(isocyanatosulfonyl)-3-furancarboxylate

methyl 4-(isocyanatosulfonyl)-3-furancarboxylate

Synthesis

Many of the compounds of Formulas I-III are prepared as shown in Equation 3 by the reaction of an appropriately substituted alkoxycarbonylthiophene or furan sulfonylisocyanate or sulfonylisothiocyanate with an appropriate aminopyrimidine or aminotriazine. These compounds of Formulas I-III can be converted to other compounds of Formulas I-III as will be shown in subsequent equations.

The novel sulfonylisocyanates are important intermediates for the preparation of the compounds of this invention. Their synthesis is described in Equations 1 and 2. ##STR54##

A mixture of the appropriate sulfonamide, e.g. an 2-alkoxycarbonyl-3-thiophene sulfonamide IV such as the methyl ester, which is known in the art, an alkyl isocyanate such as butyl isocyanate and a catalytic amount of 1,4-diaza[2.2.2]bicyclooctane (DABCO) in xylene or other inert solvent of sufficiently high boiling point (e.g.>135.degree.) is heated to approximately 130.degree.-150.degree. C. Phosgene is added to the mixture until an excess of phosgene is present as indicated by a drop in the boiling point. After the mixture is cooled and filtered to remove a small amount of insoluble by-products, the solvent and alkyl isocyanate are distilled off in-vacuo leaving a residue which is the crude sulfonyl isocyanate V. In Equation 1,

A', W' and CO.sub.2 R.sup.I are as defined previously for structures I", II" and III".

The novel sulfonylisothiocyanate intermediates of Formula Va, prepared according to Equations 2 and 2', are useful for the preparation of compounds of Formulas I-III where W=S. ##STR55##

The alkoxycarbonyl substituted sulfonamide is dissolved in dimethylformamide (DMF) with an equivalent amount of carbon disulfide and two equivalents of potassium hydroxide are added portionwise at room temperature. The mixture is stirred for 1-8 hours and diluted with ethylacetate, ethyl ether or similar aprotic solvent to cause the dipotassium salt of the dithiocarbamic acid to precipitate. The salt is isolated, dried and suspended in an inert solvent such as xylene, benzene, carbon tetrachloride or methylene chloride. Phosgene is added to the stirred suspension at below room temperature and the mixture stirred for 1-3 hours. In place of phosgene, a chloroformic ester (e.g. methyl chloroformate), phosphorous pentachloride, sulfuryl chloride or thionyl chloride can be used.

The sulfonylisothiocyanate which is formed is usually soluble in the solvent and is isolated by filtering off the insoluble potassium chloride and concentrating the filtrate. These isothiocyanates tend to be unstable and dimerize readily, (Equation 2') however, the dimers can be used

Alternate routes to prepare sulfonylisothiocyanates are described by M. O. Lozinskii et al. in Organic Compounds: Reactions and Methods, Ed. by B. A. Kazanskii et al., Vol 22, p 188-197, Plenum Press, 1973 (Engl. Trans.) ##STR56## in the same manner as the parent isothiocyanates for the purposes of this invention.

The synthetic method chosen for the preparation of compounds of Formulas I-III depends largely on the substituents QR.sup.I and R.sub.4. As shown in Equation 3, compounds of Formulas I-III wherein R.sup.I or A' are as defined for Equation 1, are conveniently prepared by reacting an appropriately substituted carbonyl thiophene or furan sulfonyl isocyanate or isothiocyanate of Formula V with an appropriately substituted aminopyrimidine or aminotriazine of Formula VI: ##STR57##

The reaction of Equation 3 is best carried out in inert aprotic organic solvents such as methylene chloride, tetrahydrofuran or acetonitrile, at ambient pressure and temperature. The mode of addition is not critical; however, it is often convenient to add the sulfonyl isocyanate or isothiocyanate to a stirred suspension of amine VI. Since such isocyanates and isothiocyanates are liquids, low melting solids or are readily soluble in solvents such as those listed above, their addition can be easily controlled.

The reaction is generally exothermic. In some cases, the desired product is soluble in the warm reaction medium and on cooling crystallizes in pure form. Other products which are soluble in the reaction medium are isolated by evaporation of the solvent, trituration of the solid residue with solvents such as 1-chlorobutane or ethyl ether, and filtration.

As shown in Equation 4, compounds of Formulas I-III, wherein W is S, A and A' are as previously defined and R.sub.5 is H, are altervatively prepared by the reaction of an appropriately substituted thiophene or furan sulfonamide with the appropriate triazine or pyrimidine isothiocyanate of Formula VIa. ##STR58##

The reaction of Equation 4 is best carried out by dissolving or suspending the sulfonamide and isothiocyanate in a polar solvent such as acetone, acetonitrile, ethyl acetate or methylethylketone, adding an equivalent of a base such as potassium carbonate and stirring the mixture at a temperature from ambient up to the reflux temperature for one to twenty-four hours. In some cases, the product precipitates from the reaction mixture and can be removed by filtration. The product is stirred in dilute mineral acid, filtered and washed with cold water. If the product does not precipitate from the reaction mixture, it can be isolated by evaporation of the solvent, trituration of the residue with dilute mineral acid and filtering off the insoluble product.

The heterocyclic isothiocyanates which are used in the procedure of Equation 4 are prepared, for example, according to the method of Japan Patent Application Pub: Kokai 51-143686, June 5, 1976, or that of W. Abraham and G. Barnikow, Tetrahedron 29, 691-7 (1973).

As shown in Equation 5, compounds of Formulas I-III, wherein A, A', R.sub.1, W', and and R.sub.5 are as defined previously, and W is O, can be prepared by methylation of salts VII wherein M is an alkali metal cation such as sodium (derived from compounds of Formulas I-III wherein R.sub.4 is hydrogen): ##STR59## D being an incipient anion and n being an integer corresponding to the valence of D.

The reaction of Equation 5 is best carried out in aprotic organic solvents such as tetrahydrofuran, dimethylformamide, or dimethylacetamide, at ambient pressure and temperature. Methylating agents VIII such as dimethyl sulfate or methyl iodide, can be employed. The desired product can be isolated by pouring the reaction mixture into water and filtering off the precipitated solid.

As shown in Equation 6, compounds of Formulas I-III wherein A, A', R.sub.1, W', and R.sub.5 are as defined for Equation 5, and W is O or S, can also be prepared by the reaction of an appropriately substituted sulfonyl-N-methylcarbamyl chloride or sulfonyl-N-methylthiocarbamyl chloride of Formula IX with an appropriate aminopyrimidine or aminotriazine of Formula VI; ##STR60##

The preparation of ureas and thioureas, like those of Formula Ic, from amines and carbamyl chlorides and thiocarbamyl chlorides is well known to the art. The reaction can best be carried out by adding equivalent amounts of chloride IX and amine VI to an inert organic solvent, such as tetrahydrofuran, xylene, or methylene chloride, in the presence of an acid acceptor, such as triethylamine, pyridine, or sodium carbonate employing temperatures from 20.degree.-130.degree.. Soluble products can be isolated by filtering off the precipitated salts and concentration of the filtrate. Insoluble products can be filtered off and washed free of salts with water.

The chlorides of Formula IX can be prepared by phosgenation or thiophosgenation of N-methylsulfonamide salts. The sulfonamide salt is added to an excess of phosgene or thiophosgene in an inert organic solvent, such as tetrahydrofuran, toluene, or xylene, whereupon, after removal of the excess phosgene, the chloride IX can be isolated or reacted in situ with the amine VI.

The esters of Formulas I-III hydrolyze to the parent acid as shown in Equation 7. Alkali metal base catalyzed hydrolysis in aqueous methanol produces the alkali metal carboxylate from which the carboxylic acid is obtained by treatment with mineral acids such as HCl: ##STR61##

The reaction of Equation 7 is best carried out in a solution containing the compound being hydrolyzed, 2 to 10 parts of methanol, 10-50 parts of water and 2-10 equivalents of a base such as sodium or potassium hydroxide maintaining the temperature at 30-90.degree. C. for 3-24 hours. the reaction yields the soluble alkali metal salt of the carboxylic acid, which is suitable for the purposes of this invention. Conversion of these salts to the acid form is easily carried out by addition to the reaction medium of strong mineral acids, such as hydrochloric or sulfuric acid, causing the desired carboxylic acids to precipitate from solution.

The acids of Formula Ie prepared as in Equation 7 wherein W is O can be converted to compounds of this invention where R.sup.I is a higher alkyl or substituted hydrocarbyl group, as already disclosed herein, by the reaction of salts of the parent acid with R.sup.I -halogen as shown in Equation 8. ##STR62##

The reaction of Equation 8 is of use where the intermediate compound R.sup.I -halogen contains a readily replaceable halogen as is the case for substituted or unsubstituted allylic or benzylic halides, .alpha.-halonitriles, or .alpha.-halocarbonyl compounds.

The procedure of Equation 8 is best carried out in inert polar solvents such as tetrahydrofuran, acetonitrile or acetone by combining the appropriately substituted carboxylic acid and base such as triethylamine or 1,4diaza[2,2,2]bicyclooctane adding the appropriate halide and heating the mixture to reflux with stirring for 1 to 16 hours. The reaction mixture can be evaporated to dryness and the residue triturated with water, filtered and washed with water to separate the desired product from the water soluble salt.

The procedure of Equation 8 can also be used for the synthesis of compounds wherein R.sup.I -halogen of Equation 8 is of a less reactive species than described above. In these cases, the silver salt of the carboxylic acid is used rather than the amine salt. The silver salt which is precipitated by adding silver nitrate to an aqueous solution of the sodium salt of the acid of Formula Ie is combined with the appropriate R.sup.I -halide using the same solvents and conditions as shown above for the amine salt.

When Q is NR.sub.6, the compounds can be prepared from the esters of this invention where R.sup.I is c.sub.1 -C.sub.4 (preferably C.sub.1) by the reaction of the esters with dialkylaluminum-N-alkylamide derivatives according to Equation 9; R.sup.I, A', W', R.sub.1, R.sub.4, R.sub.5 and R.sub.6 being as previously defined. ##STR63##

The intermediate alkylaminoaluminum compounds prepared according to A. Basha, M. Lipton and S. W. Weinreb, Tetrahedron Letters 4171 (1977), are comingled with a suspension of the esters in toluene or similar inert solvent and the mixture is refluxed for one to six hours. The product can be isolated by evaporation of the solvent, addition of methylene chloride and aqueous hydrochloric acid to decompose the residual reaction mass and extracting the desired product into the methylene chloride. Evaporation of the methylene chloride yields the desired product in sufficiently pure form for the purpose of this invention.

Compounds of Formula X, wherein Q is ##STR64## A', W' and R.sub.4 are as previously defined in the general formula, which are useful as intermediates in Equation 4, are prepared as shown in Equation 10. ##STR65## The conditions described for Equation 8 are suitable for the conversion of the esters of Formula IVa to the carboxamides as shown in Equation 10.

The products of Equation 10 are especially useful for the preparation of compounds of Formulas I-III wherein Y has an ester substituent CO.sub.2 (C.sub.1 -C.sub.6), by the route described in Equation 4.

When Q is S, these compounds can be prepared from the esters of this invention wherein QR.sup.I is O(C.sub.1 -C.sub.4 alkyl) (preferably C.sub.1) by the reaction of the esters with the appropriate dialkylaluminum alkylthiolate according to Equation 11. ##STR66##

The intermediate aluminum thiolates can be prepared according to R. P. Hatch and S. W. Weinreb, Journal of Organic Chemistry, Vol. 42, 3960 (1977). The reaction of the thiolate with the ester of this invention is best carried out in a neutral solvent such as toluene or xylene at reflux for one to three hours. Best results are obtained when the aluminum thiolate compound is present in excess of the stoichiometric amount required.

Sulfonamides of Formula IVcf are also converted from carboxylic acid esters to the thiolesters as shown in Equation 12 according to the method of R. P. Hatch and S. W. Weinreb as described for Equation 11 wherein R.sup.I, A', W' and R.sub.4 are as previously defined. ##STR67## The conditions described for Equation 11 are suitable for the conversion of the sulfonamides of Formula IVc as shown in Equation 12.

The products obtained by the procedure of Equation 12 are especially useful for the preparation of compounds of formulas I-III where Y has a substituent (CO.sub.2 C.sub.1 -C.sub.6) by the route described for Equation 4 and Q=S.

An alternate route to prepare compounds where R.sup.I is bonded to Q (Q=O) at a secondary carbon involves the reaction of the appropriate dialkylaluminum alcoholate and an ester of this invention wherein R.sup.I is a lower primary alkyl group, preferably methyl, according to Equation 13. ##STR68##

The reaction is carried out in a neutral solvent such as toluene with a boiling point sufficiently high to bring about the desired reaction during reflux. The dialkylaluminum alcoholate being present in greter than an equivalent amount to the ester for best yields. After refluxing for 1-15 hours, the reaction mixture is decomposed with dilute hydrochloric acid and the product extracted into methylene chloride. Evaporation of the methylene chloride yields the desired compound sufficiently pure for the purposes of this invention. The product can be triturated with a solvent, e.g. 1-chlorobutane to remove impurities.

Ketones wherein A is ##STR69## and A', W', W, R.sub.1, R.sub.4 and R.sub.5 are as defined by the scope of this invention, are prepared according to Equation 14, from the carboxylic acids of Formula Ie whose preparation is described in Equation 7. ##STR70##

The reaction of an organolithium compound with a carboxylic acid to yield a ketone as in Equation 14 is described in the work of H. Gilman and P. R. Van Ess, JACS, 55, 1258 (1933); H. Gilman, W. Langham and F. W. Moore, ibid., 62 (1940); C. Tegner, Chem. Scand., 6, 782 (1952); J. F. Arens and D. A. Van Dorp, Rec. Trav., 65 338 (1946); 66, 759 (1948); C. H. Depuy, G. M. Dappen, K. L. Eilers and R. A. Klein, J. Org., 29, 2813 (1964).

An excess of the organolithium compound in a suitable solvent such as diethyl ether, hexane, pentane or benzene is added to a solution or slurry of XI in a similar solvent at temperatures between -100 and 0.degree. C. The mixture is allowed to warm to room temperture and stir for 30 minutes. Aqueous acid is then added and the ketosulfonamide extracted into a suitable solvent to free it from salts followed by evaporation of the solvent.

The synthesis of a wide variety of organolithium compounds by many different procedures is known in the art. A summary of methods with bibliography is contained in Organo-Metallic Compounds, G. E. Coates, John Wiley and Sons, 1960, p. 3-21.

Oximes of the ketones of Formula XI, for example, can be prepared from the appropriate hydroxylamine derivative, wherein R.sup.III is as previously defined, and the ketone of Formula XI according to Equation 15. ##STR71##

A procedure such as that described in Preparative Organic Chemistry by G. Hilgetag and A. Martini, Ed., John Wiley and Sons, p. 513 is suitable for the preparation of the oximes of this invention.

Compounds of Formulas I-III wherein B is ##STR72## and W is O, are prepared by the sequence of reactions shown in Equation 16. ##STR73##

The compounds of Formula XVII are prepared by adding an appropriate carbon tetrahalide to a solution of a compound of Formula XII and triphenyl phosphine in an inert aprotic solvent such as acetonitrile at about -10.degree. to 25.degree. and stirring at the designated temperature for 10 to 48 hours. The carbamimidoyl halides of Formula XVI thus formed may be isolated by passing the reaction solution through a silica gel column to remove the triphenyl phosphine oxide and removal of the solvent by evaporation under reduced pressure.

The compounds of Formula XVI can be converted to the corresponding compounds of Formula XVII by treating reaction mixture with a metal alkoxide, NaOR.sup.III, at -10.degree. to 25.degree. and stirring at ambient temperature for 2 to 24 hours. The crude products of Formula XVII are isolated by filtering off the precipitated metal halide and removing the solvent by evaporation under reduced pressure. Further purification may be accomplished by recrystallization or by column chromatography over silica gel.

It will be understood that the compounds of Formula XVI are not necessarily converted directly to the compounds of Formula XVII, but may first form the carbodiimides of Formula XVIII. ##STR74##

Many compounds, particularly compounds in which the heterocyclic moiety is pyrimidinyl, may be prepared by the sequence of reactions shown in Equation 17. ##STR75##

The compounds of Formula XIX are prepared according to the procedure or R. Gompper and W. Hagele in Chemische Berichte 99, 2885-2899 (1966).

The compounds of Formula XX are prepared from the compounds of Formula XIX with sulfuryl chloride in an inert organic solvent such as methylene chloride or chloroform at temperatures between -10.degree. and 80.degree.. They are isolated by removing the solvent under reduced pressure, and can be used without further purification.

The compounds of Formual XXI are prepared in the following manner: The lithium salt of the appropriate aminoheterocycle is prepared from the aminoheterocycle with n-butyl lithium in a solvent such as tetrahydrofuran. To this salt solution is added the compound of Formula XX in tetrahydrofuran at a temperature of about -10.degree. to 10.degree.. The reaction mixture is then stirred at about 0.degree.-10.degree. for 1/2-2 hours and at ambient temperature for 1/2-4 hours. The products of Formula XXI are isolated by filtering off the inorganic salts and removing the solvent under reduced pressure. Further purification can be done by recrystallization or by column chromatography on silica gel using a suitable eluent such as ethyl acetate.

As shown in Equation 18, the compounds of Formula XXIV, wherein ##STR76## and W=S can be prepared by reacting an appropriately substituted carbamimidothioic acid salt of Formula XXII with an alkylating agent of Formula XXIII. ##STR77## wherein D is a sulfate or halogen, such as Cl, Br, or I; M is an alkali or alkaline earth metal, and n is an integer corresponding to the valence of D.

The reaction is best carried out in inert aprotic organic solvents such as tetrahydrofuran or diethyl ether at temperatures between 25.degree. and 100.degree. C. and ambient pressure. The mode of addition is not critical; however, it is often convenient to add the alkylating agent in solution to a stirred suspension of the salt of Formula XXII. The product is isolated by evaporation of the solvent and can be purified by recrystallization from a solvent such as acetonitrile or ethanol.

The metal salts of Formula XXII can be prepared by treating the corresponding sulfonylthiourea with a solution of an alkali metal or alkaline earth metal salt having an anion sufficiently basic to the proton (e.g. hydroxide, alkoxide, caronate or hydride).

When Z is N, the preferred procedure for the preparation of compounds of Formula XXIV is that shown in Equation 19. ##STR78##

A compound of Formula XXV is treated with an alkali metal (M') salt of the appropriately substituted heterocyclic amine at temperatures of 0.degree. to 100.degree. C. in a solvent such as dimethylformamide, dimethylsulfoxide or an ethereal solvent, such as tetrahydrofuran.

Compounds of Formula XXV can be prepared according to the procedure of Chem. Ber. 99, 2885 (1966).

Compounds of Formulas I-III wherein Y of group R.sub.1 contains ##STR79## and L is OH can be prepared according to the procedure of Equation 20 wherein A', W', X, R.sub.4, W and R.sub.5 are as defined previously; and Q' is C.sub.1 -C.sub.4 alkyl ##STR80## where R.sub.11 is as previously defined. ##STR81##

The reaction of Equation 20 is best carried out by suspending the compound being hydrolyzed in 10 to 100 parts of water with enough of a base such as sodium hydroxide or potassium hydroxide to obtain a pH 10 to 14, ideally a pH of 12, heating until a clear solution is obtained and then adjusting the pH to 1-3, preferably 3. The product is thus caused to precipitate in some instances and can be removed by filtration or it can be extracted into a polar organic solvent such as methylene chloride and isolated by evaporation of the solvent.

Thiophene derivatives with sulfamoyl and alkoxycarbonyl substituents on adjacent carbon atoms are prepared by the methods taught by O. Hromatka and D. Binder, U.S. Pat. No. 4,028,373 and P. A. Rossy et al., U.S. Pat. No. 4,143,050. The analogous furan derivatives are prepared similarly or as taught in Belgian Pat. No. 871,772.

Alternate methods of preparation of thiophene and furan sulfonamides with alkoxycarbonyl substituents adjacent to the sulfonamide are preferable in certain circumstances. For example, if one of the .alpha.-carbons is not substituted, chlorosulfonation of a furan or thiophene may give the undesired substituted sulfonyl chloride or a mixture of isomers. Regiospecific introduction of substituents may be achieved in many cases via ring metalation reactions. The use of such reactions has been reviewed by H. Gschwend and H. Rodriguez in "Organic Reactions", Vol. 26 (John Wiley & Sons, Inc., New York, 1979). Using these methods, the 2-lithio-3-furancarboxylates or -thiophenecarboxylates may be generated from the corresponding acid and two equivalents of an alkyllithium in an inert, aprotic solvent such as an ether solvent. These intermediates are described in ##STR82## Tetrahedron Letters 5051 (1980) and references therein. Treatment of these organolithium species with sulfur dioxide afford the corresponding 2-sulfinate-3-carboxylate salts which are conveniently isolated by evaporation of the solvent. The lithium sulfinates are converted to the sulfonamides by reaction with an excess of chloramine in aqueous solution and isolated by acidification and extraction ##STR83## into an organic solvent. Esterification of the resulting acids under standard conditions (e.g., methanol, sulfuric acid catalyst, 25.degree.-65.degree. C. 1-24 h ) yield the appropriate alkoxycarbonyl sulfonamides.

Other isomeric furan and thiophene sulfonamides may be prepared through a sequence of these metalation reactions as shown below. The reaction of 3-bromofurans or -thiophenes with alkyllithium reagents at low temperatures (preferably below -40.degree.) in an aprotic, inert solvent afford the corresponding 3-lithiofurans and -thiophenes via halogen-metal exchange. These may be quenched with sulfur dioxide to yield the 3-sulfinic acid salts. They may be subsequently ##STR84## converted to sulfonyl chlorides with a chlorinating agent, conveniently with a reagent such as N-chlorosuccinimide (NCS) in a suitable solvent such as acetic acid, preferably at ambient temperature. The ##STR85## 3-t-butylsulfonamide is then prepared upon reaction of the sulfonyl chloride with excess t-butylamine. Reaction of the sulfonamide with ##STR86## two equivalents of an alkyllithium, as described above for the 3-carboxylic acids, yield specifically the 2-lithio intermediates which are quenched with carbon dioxide to afford the 2-carboxylic acid salts. Esterification of the carboxylic acid and removal of the t-butyl group may be accomplished in one reaction by heating the above products in an alcohol solvent with acid catalyst (e.g. methanol, sulfuric acid). ##STR87##

For 3,4-disubstituted furan and thiophene sulfonamides, a modification of the above sequence is appropriate. A 4-bromo-3-t-butylsulfamoylthiophene or furan intermediate may be prepared by the methods outlined above beginning with the 3,4-dibromo compound. Reaction of these sulfonamides with ##STR88## two equivalents of alkyllithium in preferably an ether solvent at low temperature (preferably less than -40.degree.) will afford the 3-lithio species via halogenmetal exchange. These may be subsequently quenched with carbon dioxide to yield the carboxylic acids which are then converted to the free to the free sulfonamide-esters as outlined above for the 2,3-disubstituted isomers.

Compounds of structure XXIX wherein A is an aldehyde group and A' does not equal -NO.sub.2 are prepared by the procedure of Equation 21. ##STR89##

Following the procedure of R. Kanazawa and T. Tokoroyama, Synthesis, 526 (1976), a solution of sodium bis-(2-methoxyethoxy)aluminum hydride in THF is reacted with one equivalent or morpholine. To this solution at -40.degree. C. is added a methyl ester of Formula XXVIII and the solution is allowed to warm to 25.degree. C. The product is isolated by addition of aqueous acid and extraction into ether or methylene chloride. Evaporation of the solvent and crystallization or column chromatography on silica gel affords the aldehyde XXX.

Aldehydes of Formula XXX may also be prepared from the esters by treatment with diisobutylaluminum hydride according to the procedures of E. Winterfeldt, Synthesis, 617 (1975).

Compounds of Formulas I, II and III may also be prepared by the reaction of the appropriately substituted thiophene or furan sulfonamides with the appropriate heterocyclic isocyanate using the methods described in co-pending applications U.S. Ser. No. 098,725 and U.S. Ser. No. 098,722, filed Nov. 30, 1979.

The synthesis of heterocyclic amines has been reviewed in "The Chemistry of Heterocyclic Compounds" a series published by Interscience Publ., New York and London. 2-Aminopyrimidines are described by D. J. Brown in The Pyrimidines, Vol. XVI of this series. The 2-amino-1,3,5-triazines are reviewed by K. R. Huffman and in The Triazines of this same series. The synthesis of triazines are also described by F. C. Schafer, U.S. Pat. No. 3,154,547 and by K. R. Huffman and F. C. Schaeffer, J. Org. Chem. 28, 1816-1821 (1963).

The preparation of the aminoheterocycles described by Formula XXX varies according to the definition of Y.sub.1 and X.sub.II. ##STR90##

Braker, Sheehan, Spitzmiller and Lott, J. Am. Chem. Soc. 69, 3072 (1947) describes the preparation of 6,7-dihydro-4-methoxy-5H-cyclopentapyrimidin-2-amine by the following sequence of reactions. ##STR91##

Similarly, 6,7-dihydro-4-methyl-5H-cyclopentapyrimidin-2-amine can be prepared by the condensation of 2-acetylcyclopentanone with guanidine carbonate, but preferably under acidic conditions, removing the water formed. ##STR92##

Shrage and Hitchings, J. Org. Chem. 16, 1153 (1951) described the preparation of 5,6-dihydro-4-methylfuro [2,3-d]pyrimidin-2-amine by the following sequence of reactions ##STR93##

5,6-Dihydro-4-methoxyfuro [2,3-d]pyrimidin-2-amine can be prepared by the method of Braker et al., J. Am. Chem. Soc. 69, 3072 (1947), using 5,6-dihydro-4-hydroxyfuro [2,3-d]pyrimidin-2-amine [Svab, Budesinski and Vavrina, Collection Czech. Chem. Commun. 32, 1582 (1967)]. ##STR94##

Caldwell, Kornfeld and Donnell, J. Am. Chem. Soc. 63, 2188 (1941), describe the preparation of 6,7-dihydro-5H-cyclopentapyrimidin-2-amine by the following sequence of reactions. ##STR95##

Fissekis, Myles and Brown, J. Org. Chem. 29, 2670 (1964), describe the preparation of 2-amino-4-hydroxy-5-(2-hydroxyethyl) pyrimidine which can be converted to 5,6-dihydrofuro [2,3-d]pyrimidin-2-amine by dehydration. ##STR96##

Agriculturally suitable salts of compounds of Formulas I-III are also useful herbicides and can be prepared by a number of ways known to the art. For example, metal salts can be made by treating compounds of Formulas I-III with a solution of alkali or alkaline earth metal salt having a sufficiently basic anion (e.g., hydroxide, alkoxide, carbonate or hydride). Quaternary amine salts can be made by similar techniques.

Salts of compounds of Formulas I-III can also be prepared by exchange of one cation to another. Cationic exchange can be effected by direct treatment of an aqueous solution of a salt of a compound of Formulas I-III (e.g., alkali metal or quaternary amine salt) with a solution containing the cation to be exchanged. This method is most effective when the desired salt containing the exchanged cation is insoluble in water, e.g., a copper salt, and can be separated by filtration.

Exchange may also be effected by passing an aqueous solution of a salt of a compound of Formulas I-III (e.g., an alkali metal or quaternary amine salt) through a column packed with a cation exchange resin containing the cation to be exchanged. In this method, the cation of the resin is exchanged for that of the original salt and the desired product is eluted from the column. This method is particularly useful when the desired salt is water soluble, e.g., a potassium, sodium or calcium salt.

Acid addition salts, useful in this invention, can be obtained by reacting a compound of Formulas I-III with a suitable acid, e.g., p-toluenesulfonic acid, trichloroacetic acid or the like.

The compounds of this invention and their preparation are further illustrated by the following examples wherein temperatures are given in degrees centrigrade.

The desired product is underscored at the top of each example.

EXAMPLE 1

2-Methoxycarbonyl-3-thiophenesulfonyl isocyanate

A mixture containing 22.1 g of methyl-3-sulfamoylthiophene-2-carboxylate, 9.9 g of n-butyl isocyanate, 0.3 g of 1,4-diaza[2,2,2]bicyclooctane and 150 ml of dry xylene was placed in a 4 neck round bottom flask equipped with a gas inlet tube, mechanical stirrer, thermometer and dry ice cooled reflux condenser. This mixture was heated to 135.degree. C. and phosgene was passed into the flask so that after several minutes, the reflux temperature dropped to 120.degree.. The phosgene addition was halted until the temperature rose to 130.degree. and then additional phosgene was added to cause the temperature to drop again to 120.degree.. The phosgene addition cycle was repeated until the reflux temperature of the reaction mixture remained at 120.degree. with no further phosgene addition.

Cooling the reaction mixture caused a small amount of a precipitate to form which was removed by filtration and the filtrate was concentrated in-vacuo to yield an oil which showed a stong absorption peak in the infrared region at 2200 cm.sup.1 consistent for the desired sulfonyl isocyanate. This highly reactive intermediate was used without further purification.

EXAMPLE 2

Methyl 3-[[(4,6-dimethylpyrimidin-2-yl)aminocarbonyl]-aminosulfonyl]-2-thiophenec arboxylate

To 1.23 g of 2-amino-4,6-dimethyl pyrimidine in 30 ml of anhydrous acetonitrile was added with stirring 2.7 g of 2-methoxycarbonyl-3-thiophene-sulfonylisocyanate. The mixture was heated to the boiling point, whereupon all of the insoluble material dissolved and the mixture was allowed to cool. After stirring for two hours the mixture was filtered to remove the desired product which had precipitated as a white solid. After washing with anhydrous ethyl ether the produce melted at 191.degree.-193.degree. with decomposition and showed absorption peaks by nuclear magnetic resonance at 3.8 ppm for the methoxy group, 2.44 ppm for the two methyl groups on the pyrimidine ring, a peak at 7.0 consistent for the hydrogen in the pyrimidine ring and a peak at 7.42 for the hydrogens on the thiophene ring. The infrared absorption spectrum showed absorption peaks at 1720 and 1700 cm-.sup.1 consistent for the two carbonyl groups present in the desired product.

EXAMPLE 3

Methyl 3 [[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]-aminosulfonyl] -2-thiophenecarboxylate

To 1.5 g of 2-amino-4,6-dimethoxypyrimidine in 30 ml of anhydrous acetonitrile was added 2.7 g of 2-methoxycarbonyl-3-thiopnenesulfonyl isocyanate with stirring at ambient temperature. All of the solid reactant dissolved and after twenty minutes of stirring a preciptate started to form. After two hours the mixture was filtered and the solid which was washed with anhydrous ethyl ether, melted at 191.degree.-193.degree.. The solid showed peaks by nuclear magnetic resonance spectroscopy at 4.0 ppm and 3.8 ppm for the methoxy groups, 6.0 ppm for the H of pyrimidine and 7.6 ppm for the hydrogens on thiophene. The infrared absorption spectrum showed absorption peaks at 1730 and 1700 cm-.sup.1 consistent for the two carbonyl peaks in the desired product.

EXAMPLE 4

Methyl 3-[[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]aminosulfonyl]-2-thiop henecarboxylate

To 1.4 g of 2-amino-4-methoxy-6-methylpyrimidine in 30 ml of anhydrous acetonitrile was added at ambient temperature, with stirring 3.6 g of 2-methoxycarbonyl-3-thiophenesulfonylisocyanate. The mixture was heated to the boiling point and then allowed to cool to ambient temperature. After stirring for sixteen hours the precipitate present in the mixture was filtered off and washed with anhydrous ethyl ether. The product thus obtained which melted at 165.degree.-173.degree. showed absorption peaks by infrared spectroscopy at 1720 and 1700 cm-.sup.1, consistent for the carbonyl groups in the desired product.

EXAMPLE 5

Methyl 3-[[(4,6-dimethyl-1,3,5-triazin-2-yl) aminocarbonyl]aminosulfonyl]-2-thiophenecarboxylate

To 1.23 g of 2-amino-4,6-dimethyl-1,3,5-triazine in 30 ml of anhydrous methylene chloride was added with stirring 2.7 g of 2-methoxycarbonyl-3-thiophenesulfonylisocyanate. The mixture was heated to the boiling point and allowed to cool and stir at ambient temperature for sixteen hours. The solid thus obtained was removed by filtration to yield 2.3 g of the crude desired product melting at 158.degree.-178.degree.. The product showed peaks at 1720 and 1700 cm-.sup.1, by infrared absorption spectroscopy, consistent for the desired product.

EXAMPLE 6

Methyl 3-[[(5,6 dimethyl-1,2,4-triazinyl-2-yl)aminocarbonyl]aminosulfonyl]-2-thiophenecarb oxylate

To 1.2 g of 3-amino-5,6-dimethyl-1,2,4-traizine in 30 ml of anhydrous methylene chloride was added with stirring 2.7 g of 2-methoxycarbonyl-3-thiophenesulfonylisocyanate. After stirring for 16 hours at ambient temperature the solution was filtered to remove some insoluble material and the filtrate evaporated to dryness. The residue thus obtained was triturated with ethyl ether and the insoluble product filtered to yield 2.9 g of the desired compound melting at 129.degree. with decomposition. Infrared analysis of this product showed absorption peaks at 1730 and 1700 cm-.sup.1 as expected for the desired product.

EXAMPLE 7

3-[[(4,6-Dimethylpyrimidin-2-yl)aminocarbonyl]amino sulfonyl]-2-thiophene carboxylic acid

A solution of 1.0 g of methyl 3-[[(4,6-dimethylpyrimidin-2-yl)aminocarbonyl]aminosulfonyl]-2-thiopheneca rboxylate in 10 ml of ethanol and 1 ml of 50% sodium hydroxide in water was stirred overnight at room temperature. To this was added icewater and aqueous hydrochloric acid until acidic, and the precipitate was filtered and washed first with acetone and then with methylene chloride. The product, 0.8 g, melted at 127.degree..

EXAMPLE 8

1-[3-[[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]aminosulfonyl]thiene -2-yl carbonyl]pyrrolidone

To 2.5 ml of 2M-solution of trimethylaluminum in toluene was added 20 ml of methylene chloride and 400 .mu.l of pyrrolidine. To this solution was added 0.66 g of methyl 3-[[(4-methoxy-6-methylpyrimidin-2-yl)amino carbonyl]aminosulfonyl]-2-thiophenecarboxylate. The resulting solution was stirred under nitrigen overnight at room temperature, quenched with 5N aqueous hydrochloric acid, and extracted with ethyl acetate. The residue obtained from evaporation of solvent was washed with ether to afford 0.6 g of product, mp 184.degree.-5.degree., which showed absorption peaks at 1.8-2.2 ppm and 3.2-3.8 ppm for the pyrrolidine ring and no methyl ester peak, and all other signals indicative of the desired product.

                                      TABLE I-a
    __________________________________________________________________________
     ##STR97##
    A'    R.sup.I      W R.sub.5
                            X     Y              m.p. (.degree.C.)
    __________________________________________________________________________
    H     CH.sub.3     O H  CH.sub.3
                                  Cl
    H     CH.sub.3     O H  H     H
    H     CH.sub.3     O H  Cl    Cl
    H     CH.sub.3     O H  OCH.sub.2 CH.sub.3
                                  CH.sub.2 CH.sub.3
    H     CH.sub.3     O H  CH.sub.3
                                  CH.sub.2 CH.sub.3
    H     CH.sub.3     O H  CH.sub.3
                                  CH.sub.3 CH.sub.2 OCH.sub.3
    H     CH.sub.3     O H  CH.sub.3
                                  (CH.sub.2).sub.4 OCH.sub.3
    H     CH.sub.3     O H  CH.sub.3
                                  (CH.sub.2).sub.2 OC.sub.2 H.sub.5
    H     CH.sub.3     O H  OCH.sub.3
                                  CH.sub.2 CN
    H     CH.sub.3     O H  OCH.sub.3
                                   ##STR98##
    H     CH.sub.3     O H  OCH.sub.3
                                  (CH.sub.2).sub.3 CO.sub.2 CH.sub.3
    H     CH.sub.3     O H  OCH.sub.3
                                  CH.sub.2 CO.sub.2 C.sub.2 H.sub.5
    H     CH.sub.3     O H  OCH.sub.3
                                  CH.sub.2 CF.sub.3
    H     CH.sub.3     O H  OCH.sub.3
                                  CH.sub.2 CH.sub.2 Cl
    H     CH.sub.3     O H  OCH.sub.3
                                  CF.sub.3
    H     CH.sub.3     O H  OCH.sub.3
                                  CH.sub.2 CCl.sub.3
    H     CH.sub.3     O H  OCH.sub.3
                                  (CH.sub.2).sub.4 Cl
    H     CH.sub.3     O H  OCH.sub.3
                                  (CH.sub.2).sub.3 Br
    H     CH.sub.3     O H  OCH.sub.3
                                  CH.sub.2 CHCH.sub.2
    H     CH.sub.3     O H  OCH.sub.3
                                  CH.sub.2 CHCHCH.sub.2
    H     CH.sub.3     O H  CH.sub.3
                                  O(CH.sub.2).sub.2 OCH.sub.3
    H     CH.sub.3     O H  CH.sub.3
                                  O(CH.sub.2).sub.2 OC.sub.2 H.sub.5
    H     CH.sub.3     O H  CH.sub.3
                                  O(CH.sub.2).sub.2 OCH(CH.sub.3).sub.2
    H     CH.sub.3     O H  CH.sub.3
                                  O(CH.sub.2).sub.3 O(CH.sub.2).sub.2
                                  CH.sub.3
    H     CH.sub.3     O H  CH.sub.3
                                   ##STR99##
    H     CH.sub.3     O H  CH.sub.3
                                   ##STR100##
    H     CH.sub.3     O H  CH.sub.3
                                   ##STR101##
    H     CH.sub.3     O H  CH.sub.3
                                   ##STR102##
    H     CH.sub.3     O H  CH.sub.3
                                   ##STR103##
    H     CH.sub.3     O H  CH.sub.3
                                   ##STR104##
    H     CH.sub.3     O H  CH.sub.3
                                   ##STR105##
    H     CH.sub.3     O H  CH.sub.3
                                   ##STR106##
    H     CH.sub.3     O H  CH.sub.3
                                   ##STR107##
    H     CH.sub.3     O H  CH.sub.3
                                   ##STR108##
    H     CH.sub.3     O H  CH.sub.3
                                   ##STR109##
    H     CH.sub.3     O H  CH.sub.3
                                  SCN
    H     CH.sub.3     O H  CH.sub.3
                                  N.sub.3
    H     CH.sub.3     O H  CH.sub.3
                                  NH.sub.2
    H     CH.sub.3     O H  CH.sub.3
                                  NHCH.sub.3
    H     CH.sub.3     O H  CH.sub.3
                                   ##STR110##
    H     CH.sub.3     O H  CH.sub.3
                                   ##STR111##
    H     CH.sub.3     O H  CH.sub.3
                                   ##STR112##
    H     CH.sub.3     O H  CH.sub.3
                                   ##STR113##
    H     CH.sub.3     O H  CH.sub.3
                                  NHCH.sub.2 CHCH.sub.2
    H     CH.sub.3     O H  CH.sub.3
                                  NHCH.sub.2 CHCHCH.sub.2
    H     CH.sub.3     O H  CH.sub.3
                                   ##STR114##
    H     CH.sub.3     O H  CH.sub.3
                                   ##STR115##
    H     CH.sub.3     O H  CH.sub.3
                                  NH(CH.sub.2).sub.2 OC.sub.2 H.sub.5
    H     CH.sub.3     O H  CH.sub.3
                                   ##STR116##
    H     CH.sub.3     O H  CH.sub.3
                                   ##STR117##
    H     CH.sub.3     O H  CH.sub.3
                                   ##STR118##
    H     CH.sub.3     O H  CH.sub.3
                                   ##STR119##
    H     CH.sub.3     O H  CH.sub.3
                                   ##STR120##
    H     CH.sub.3     O H  CH.sub.3
                                   ##STR121##
    H     CH.sub.3     O H  CH.sub.3
                                   ##STR122##
    H     CH.sub.3     O H  CH.sub.3
                                  OC.sub.2 H.sub.5
    H     CH.sub.3     O H  CH.sub. 3
                                  On-C.sub.3 H
    H     CH.sub.3     O H  CH.sub.3
                                  OCH(CH.sub.3).sub.2
    H     CH.sub.3     O H  CH.sub.3
                                   ##STR123##
    H     CH.sub.3     O H  CH.sub.3
                                  OCH.sub.2 CF.sub.3
    H     CH.sub.3     O H  CH.sub.3
                                  OCH.sub.2 CH.sub.2 Cl
    H     CH.sub.3     O H  CH.sub.3
                                  OCH.sub.2 CH.sub.2 Br
    H     CH.sub.3     O H  CH.sub.3
                                  OCH.sub.2 CCl.sub.3
    H     CH.sub.3     O H  CH.sub.3
                                  OCH.sub.2 CN
    H     CH.sub.3     O H  CH.sub.3
                                   ##STR124##
    H     CH.sub.3     O H  CH.sub.3
                                  OCH.sub.2CHCHCH.sub.3
    H     CH.sub.3     O H  CH.sub.3
                                  OCH.sub.2CCH
    H     CH.sub.3     O H  CH.sub.3
                                  OCH.sub.2CCCH.sub.2 Cl
    H     CH.sub.3     O H  CH.sub.3
                                   ##STR125##
    H     CH.sub.3     O H  CH.sub. 3
                                   ##STR126##
    H     CH.sub.3     O H  CH.sub.3
                                  SCH.sub.3
    H     CH.sub.3     O H  CH.sub.3
                                  SCH(CH.sub.3).sub.2
    H     CH.sub.3     O H  CH.sub.3
                                  Sn-C.sub.4 H.sub.9
    H     CH.sub.3     O H  CH.sub.3
                                  SCH.sub.2 CHCH.sub.2
    5-CH.sub.3
          CH.sub.3     O H  CH.sub.3
                                  OCH.sub.3
    5-CH.sub.3
          CH.sub.3     O H  CH.sub.3
                                  OCH.sub.3
    5-Cl  CH.sub.3     O H  CH.sub.3
                                  OCH.sub.3
    5-Cl  CH.sub.3     O H  CH.sub.3
                                  OCH.sub.3
    5-Cl  CH.sub.3     O H  CH.sub.3
                                  OCH.sub.3
    5-Br  CH.sub.3     O H  CH.sub.3
                                  OCH.sub.3
    5-Br  CH.sub.3     O H  CH.sub.3
                                  OCH.sub.3
    5-Br  CH.sub.3     O H  CH.sub.3
                                  OCH.sub.3
    5-C.sub.2 H.sub.5
          CH.sub.3     O H  CH.sub.3
                                  OCH.sub.3
    5-n-C.sub.4 H.sub.9
          CH.sub.3     O H  CH.sub.3
                                  OCH.sub.3
    H     (CH.sub.2).sub.5 CN
                       O H  CH.sub.3
                                  OCH.sub.3
    H     CH.sub.2 CHCH(CH.sub.2).sub.2 Cl
                       O H  CH.sub.3
                                  OCH.sub.3
    H     CH.sub.2 CCCH.sub.2 Cl
                       O H  CH.sub.3
                                  OCH.sub.3
    H     CH.sub.2 CC(CH.sub.2).sub.3 Cl
                       O H  CH.sub.3
                                  OCH.sub.3
           ##STR127##  O H  CH.sub.3
                                  OCH.sub.3
    H
           ##STR128##  O H  CH.sub.3
                                  OCH.sub.3
    H
           ##STR129##  O H  CH.sub.3
                                  OCH.sub.3
    H
           ##STR130##  O H  CH.sub.3
                                  OCH.sub.3
    H
           ##STR131##  O H  CH.sub.3
                                  OCH.sub.3
    H
           ##STR132##  O H  CH.sub.3
                                  OCH.sub.3
    H
           ##STR133##  O H  CH.sub.3
                                  OCH.sub.3
    H
           ##STR134##  O H  CH.sub.3
                                  OCH.sub.3
    H
           ##STR135##  O H  CH.sub.3
                                  OCH.sub.3
    H
           ##STR136##  O H  CH.sub.3
                                  OCH.sub.3
    H
           ##STR137##  O H  CH.sub.3
                                  OCH.sub.3
    H     CH.sub.3     O H  OCH.sub.3
                                  SCH.sub.2CCH
    H     CH.sub.3     O H  OCH.sub.3
                                   ##STR138##
    H     CH.sub.3     O H  OCH.sub.3
                                  SCH.sub.2 CN
    H     CH.sub.3     S H  OCH.sub.3
                                  CH.sub.3
    H     CH.sub.3     S H  CH.sub.3
                                  CH.sub.3
    H     CH.sub.3     S H  OCH.sub.3
                                  CH.sub.3
    H     CH.sub.3     S H  OCH.sub.3
                                  CH.sub.3
    H     CH.sub.3     S CH.sub.3
                            OCH.sub.3
                                  OCH.sub.3
    H     CH.sub.3     S CH.sub.3
                            CH.sub.3
                                  OCH.sub.3
    H     CH.sub.3     S H  OCH.sub.3
                                  OC.sub.2 H.sub.5
    H     CH.sub.3     O CH.sub.3
                            OCH.sub.3
                                  OCH.sub.3
    H     CH.sub.3     O CH.sub.3
                            CH.sub.3
                                  OCH.sub.3
    H     CH.sub.3     O CH.sub.3
                            CH.sub.3
                                  CH.sub.3
    H     CH.sub.3     O CH.sub.3


CH.sub.3 OCH.sub.2 CO.sub.2 CH.sub.3 4-Cl CH.sub.3 O H CH.sub.3 OCH.sub.3 4-Cl CH(CH.sub.3).sub.2 O H CH.sub.3 OCH.sub.3 4-Cl CH.sub.2 CHCH.sub.2 O H CH.sub.3 OCH.sub.3 4-Br C.sub.2 H.sub.5 O H CH.sub.3 OCH.sub.3 4-CH.sub.3 CH.sub.3 CH.sub.2 Cl O H CH.sub.3 OCH.sub.3 4-C.sub.2 H.sub.5 CH(CH.sub.3).sub.2 O H CH.sub.3 OCH.sub.3 4-n-C.sub.4 H.sub.9 CH.sub.2 CHCH.sub.2 O H CH.sub.3 OCH.sub.3 4-i-C.sub.3 H.sub.7 CH.sub.3 O H CH.sub.3 OCH.sub.3 5-Cl C.sub.2 H.sub.3 O H CH.sub.3 OCH.sub.3 5-Br CH.sub.3 O H CH.sub.3 OCH.sub.3 5-CH.sub.3 CH(CH.sub.3).sub.2 O H CH.sub.3 OCH.sub.3 H C.sub.2 H.sub.5 O H CH.sub.3 OCH.sub.3 H CH.sub.2 CHCH.sub.2 O H OCH.sub.3 OCH.sub.3 H (CH.sub.2).sub.3 CH.sub.3 O H OCH.sub.3 OCH.sub.3 H (CH.sub.2).sub.4 CH.sub.3 O H OCH.sub.3 OCH.sub.3 H ##STR139## O H OCH.sub.3 OCH.sub.3 H (CH.sub.2).sub.5 CH.sub.3 O H OCH.sub.3 OCH.sub.3 H CH.sub.2 CHCHCH.sub.3 O H OCH.sub.3 OCH.sub. 3 H CH.sub.2 CHCHC.sub.2 H.sub.5 O H OCH.sub.3 OCH.sub.3 H CH.sub.2 CHCHCH(.sub.3).sub.2 O H OCH.sub.3 OCH.sub.3 H (CH.sub.2).sub.3 Cl O H OCH.sub.3 OCH.sub.3 H (CH.sub.3).sub.5 Cl O H OCH.sub.3 OCH.sub.3 H (CH.sub.2).sub.6 OCH.sub.3 O H OCH.sub.3 OCH.sub.3 H CH.sub.2 CN O H OCH.sub.3 OCH.sub.3 4-OCH.sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 5-OCH.sub.3 CH.sub.3 O H CH.sub.3 OCH.sub.3 4-NO.sub.2 CH.sub.3 O H CH.sub.3 OCH.sub.3 5-NO.sub.2 CH.sub.3 O H CH.sub.3 OCH.sub.3 4-CF.sub.3 CH.sub.3 O H CH.sub.3 OCH.sub.3 5-CF.sub.3 CH.sub.3 O H CH.sub.3 OCH.sub.3 H CH.sub.2 CH.sub.2 CH.sub.2 Cl O H CH.sub.3 OCH.sub.3 H CH.sub.2 CCl.sub.3 O H CH.sub.3 OCH.sub.3 H (CH.sub.2).sub.6 Cl O H CH.sub.3 OCH.sub.3 H (CH.sub.2).sub.4 Cl O H CH.sub.3 OCH.sub.3 H CH.sub.2 CBr.sub.3 O H CH.sub.3 OCH.sub.3 H (CH.sub.2).sub. 4 Br O H CH.sub.3 OCH.sub.3 H (CH.sub.2).sub.6 Br O H CH.sub.3 OCH.sub.3 H (CH.sub.2).sub.6 F O H CH.sub.3 OCH.sub.3 H (CH.sub.2).sub.4 F O H CH.sub.3 OCH.sub.3 H (CH.sub.2).sub.3 F O H CH.sub.3 OCH.sub.3 H CH.sub.2 CF.sub.3 O H CH.sub.3 OCH.sub.3 H CH.sub.2 CN O H CH.sub.3 OCH.sub.3 H ##STR140## O H CH.sub.3 OCH.sub.3 H ##STR141## O H CH.sub.3 OCH.sub.3 H ##STR142## O H CH.sub.3 OCH.sub.3 H ##STR143## O H CH.sub.3 OCH.sub.3 H ##STR144## O H CH.sub.3 OCH.sub.3 H ##STR145## O H CH.sub.3 OCH.sub.3 H ##STR146## O H CH.sub.3 OCH.sub.3 H ##STR147## O H CH.sub.3 OCH.sub.3 `-H CH.sub.2 OCH.sub.3 O H CH.sub.3 OCH.sub.3 H CH.sub.2 OC.sub.2 H.sub.5 O H CH.sub.3 OCH.sub.3 H CH.sub.2 OCH(CH.sub.3).sub.2 O H CH.sub.3 OCH.sub.3 H CH.sub.2 On-C.sub.4 H.sub.9 O H CH.sub.3 OCH.sub.3 H H O H CH.sub.3 CH.sub.3 H H O H CH.sub.3 OCH.sub.3 H H O H OCH.sub.3 OCH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.3 191-193 H CH.sub.3 O H OCH.sub.3 OCH.sub.3 191-193 H CH.sub.3 O H OCH.sub.3 CH.sub.3 165-173 H CH.sub.2 C.sub.6 H.sub.5 O H CH.sub.3 CH.sub.3 133-136 H CH(CH.sub.3).sub.2 O H OCH.sub.3 OCH.sub.3 155-160 H CH.sub.2 CHCH.sub.2 O H CH.sub.3 OCH.sub.3 164-165 H CH(CH.sub.3).sub.2 O H CH.sub.3 OCH.sub. 3 153-161 H CH(CH.sub.3)C.sub.2 H.sub.5 O H CH.sub.3 OCH.sub.3 146-156 H CH(CH.sub.3)CHCH.sub.2 O H CH.sub.3 OCH.sub.3 152-154 H CH(CH.sub.3)CCH O H CH.sub.3 OCH.sub.3 167-173 H CH.sub.3 O H CH.sub.3 CF.sub.3 171-175 H CH.sub.3 O H CH.sub.3 SCH.sub.3 128-142 H CH.sub.3 O H CH.sub.3 CH.sub.2 OCH.sub.3 183-187 H CH.sub.3 O H CH.sub.3 Cl 155-158 H CH.sub.3 O H CH.sub.3 N(CH.sub.3).sub.2 225-228 H CH.sub.3 O H Cl N(CH.sub.3).sub.2 205-207 H CH.sub.3 O H CH.sub.3 CH.sub.3 198-199 H CH.sub.2 CHCH.sub.2 O H CH.sub.3 CH.sub.3 173-175(d) H CH.sub.2 CHCH.sub.2 O H OCH.sub.3 OCH.sub.3 140-145(d) H CH.sub.3 O H CH.sub.3 H 184-185(d) H CH.sub.3 O H CH.sub.3 C.sub.2 H.sub.5 160-169 H CH.sub.3 O H CH.sub.3 CH(CH.sub.3).sub.2 130-139 H CH(CH.sub.3)CCH O H CH.sub.3 CH.sub.3 -- H CH.sub.3 O H CH.sub.3 N(CH.sub.3)OCH.sub.3 150-154(d) __________________________________________________________________________

TABLE I-b ______________________________________ ##STR148## m.p. A' R.sup.I W R.sub.5 X Y (.degree.C.) ______________________________________ H CH.sub.3 O H CH.sub.3 Cl H CH.sub.3 O H H H H CH.sub.3 O H Cl Cl H CH.sub.3 O H OCH.sub.2 CH.sub.3 CH.sub.2 CH.sub.3 H CH.sub.3 O H CH.sub.3 CH(CH.sub.3).sub.2 H CH.sub.3 O H CH.sub.3 CH.sub.2 CH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.2 OCH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.3 CH.sub.2 OCH.sub.3 H CH.sub.3 O H CH.sub.3 (CH.sub.2).sub.4 OCH.sub.3 H CH.sub.3 O H CH.sub.3 (CH.sub.2).sub.2 OC.sub.2 H.sub.5 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CN H CH.sub.3 O H OCH.sub.3 ##STR149## H CH.sub.3 O H OCH.sub.3 (CH.sub.2).sub.3 CO.sub.2 CH.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CO.sub.2 C.sub.2 H.sub.5 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CF.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CH.sub.2 Cl H CH.sub.3 O H OCH.sub.3 CF.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CCl.sub.3 H CH.sub.3 O H OCH.sub.3 (CH.sub.2).sub.4 Cl H CH.sub.3 O H OCH.sub.3 (CH.sub.2).sub.3 Br H CH.sub.3 O H OCH.sub.3 CH.sub.2 CHCH.sub.2 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CHCHCH.sub.2 H CH.sub.3 O H CH.sub.3 O(CH.sub.2).sub.2 OCH.sub.3 H CH.sub.3 O H CH.sub.3 O(CH.sub.2).sub.3 OC.sub.2 H.sub.5 H CH.sub.3 O H CH.sub.3 O(CH.sub.2).sub. 2 OCH(CH.sub.3).sub.2 H CH.sub.3 O H CH.sub.3 CH.sub.3 179- 181(d) H CH.sub.3 O H OCH.sub.3 CH.sub.3 149- 159(d) H CH.sub.3 O H OCH.sub.3 OCH.sub.3 189- 190(d) ______________________________________

TABLE I-c __________________________________________________________________________ ##STR150## A' R.sup.I W R.sub.5 X Y m.p. (.degree.C.) __________________________________________________________________________ H CH.sub.3 O H CH.sub.3 Cl H CH.sub.3 O H H H H CH.sub.3 O H Cl Cl H CH.sub.3 O H OCH.sub.2 CH.sub.3 CH.sub.2 CH.sub.3 H CH.sub.3 O H CH.sub.3 CH(CH.sub.3).sub.2 H CH.sub.3 O H CH.sub.3 CH.sub.2 CH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.3 CH.sub.2 OCH.sub.3 H CH.sub.3 O H CH.sub.3 (CH.sub.2).sub.4 OCH.sub.3 H CH.sub.3 O H CH.sub.3 (CH.sub.2).sub.2 OC.sub.2 H.sub.5 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CN H CH.sub.3 O H OCH.sub.3 ##STR151## H CH.sub.3 O H OCH.sub.3 (CH.sub.2).sub.3 CO.sub.2 CH.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CO.sub.2 C.sub.2 H.sub.5 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CF.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CH.sub.2 Cl H CH.sub.3 O H OCH.sub.3 CF.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CCl.sub.3 H CH.sub.3 O H OCH.sub.3 (CH.sub.2).sub.4 Cl H CH.sub.3 O H OCH.sub.3 (CH.sub.2).sub.3 Br H CH.sub.3 O H OCH.sub.3 CH.sub.2 CHCH.sub.2 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CHCHCH.sub.2 H CH.sub.3 O H CH.sub.3 O(CH.sub.2).sub.2 OCH.sub.3 H CH.sub.3 O H CH.sub.3 O(CH.sub.2).sub.3 OC.sub.2 H.sub.5 H CH.sub.3 O H CH.sub.3 O(CH.sub.2).sub.2 OCH(CH.sub.3).sub.2 H CH.sub.3 O H CH.sub.3 OCH.sub.3 182-183.5 H CH.sub.3 O H CH.sub.3 CH.sub.3 169-172(d) H CH.sub.3 O H OCH.sub.3 OCH.sub.3 179-181 H CH.sub.3 O H CH.sub.3 CH.sub.2 OCH.sub.3 154-157(d) 5-C.sub.2 H.sub.5 CH.sub.3 O H CH.sub.3 CH.sub.3 180-185 5-C.sub.2 H.sub.5 CH.sub.3 O H CH.sub.3 OCH.sub.3 150-154(d) 5-C.sub.2 H.sub.5 CH.sub.3 O H OCH.sub.3 OCH.sub.3 158-161 __________________________________________________________________________

TABLE I-d __________________________________________________________________________ ##STR152## A' R.sup.I W R.sub.5 X Y m.p. (.degree.C.) __________________________________________________________________________ H CH.sub.3 O H CH.sub.3 Cl H CH.sub.3 O H H H H CH.sub.3 O H Cl Cl H CH.sub.3 O H OCH.sub.2 CH.sub.3 CH.sub.2 CH.sub.3 H CH.sub.3 O H CH.sub.3 CH(CH.sub.3).sub.2 H CH.sub.3 O H CH.sub.3 CH.sub.2 CH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.2 OCH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.3 CH.sub.2 OCH.sub.3 H CH.sub.3 O H CH.sub.3 (CH.sub.2).sub.4 OCH.sub.3 H CH.sub.3 O H CH.sub.3 (CH.sub. 2).sub.2 OC.sub.2 H.sub.5 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CN H CH.sub.3 O H OCH.sub.3 ##STR153## H CH.sub.3 O H OCH.sub.3 (CH.sub.2).sub.3 CO.sub.2 CH.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CO.sub.2 C.sub.2 H.sub.5 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CF.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CH.sub.2 Cl H CH.sub.3 O H OCH.sub.3 CF.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CCl.sub.3 H CH.sub.3 O H OCH.sub.3 (CH.sub.2).sub.4 Cl H CH.sub.3 O H OCH.sub.3 (CH.sub.2).sub.3 Br H CH.sub.3 O H OCH.sub.3 CH.sub.2 CHCH.sub.2 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CHCHCH.sub.2 H CH.sub.3 O H CH.sub.3 O(CH.sub.2).sub.2 OCH.sub.3 H CH.sub.3 O H CH.sub.3 O(CH.sub.2).sub.3 OC.sub.2 H.sub.5 H CH.sub.3 O H CH.sub.3 O(CH.sub.2).sub.2 OCH(CH.sub.3).sub.2 H CH.sub. 3 O H CH.sub.3 CH.sub.3 158-171 H CH.sub.3 O H OCH.sub.3 OCH.sub.3 181-183 H CH.sub.3 O H CH.sub.3 OCH.sub.3 166-170 H CH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 195-196(d) H CH(CH.sub.3).sub.2 O H CH.sub.3 OCH.sub.3 179-181(d) H CH(CH.sub.3).sub.2 O H OCH.sub.3 OCH.sub.3 178-180(d) H CH.sub.2 CHCH.sub.2 O H CH.sub.3 OCH.sub.3 142-146(d) H CH.sub.2 CHCH.sub.2 O H OCH.sub.3 OCH.sub.3 151-155(d) H CH.sub.3 O H OCH.sub.3 N(CH.sub.3).sub.2 173-175 H CH.sub.3 O H OCH.sub.3 CH.sub.2 OCH.sub.3 179-181 H CH.sub.3 O CH.sub.3 OCH.sub.3 OCH.sub.3 185-187 H CH.sub.3 O CH.sub.3 CH.sub.3 Cl 134-138 H CH.sub.3 O CH.sub.3 OCH.sub.3 CH.sub.3 139-145 H CH.sub.3 O OCH.sub.3 OCH.sub.3 OCH.sub.3 175-177 __________________________________________________________________________

TABLE I-e __________________________________________________________________________ ##STR154## A' R.sup.I W R.sub.5 X Y m.p.(.degree.C.) __________________________________________________________________________ H CH.sub.3 O H CH.sub.3 Cl H CH.sub.3 O H H H H CH.sub.3 O H Cl Cl H CH.sub.3 O H OCH.sub.2 CH.sub.3 CH.sub.2 CH.sub.3 H CH.sub.3 O H CH.sub.3 CH(CH.sub.3).sub.2 H CH.sub.3 O H CH.sub.3 CH.sub.2 CH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.2 OCH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.3 CH.sub.2 OCH.sub.3 H CH.sub.3 O H CH.sub.3 (CH.sub.2).sub.4 OCH.sub.3 H CH.sub.3 O H CH.sub.3 (CH.sub.2).sub.2 OC.sub.2 H.sub.5 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CN H CH.sub.3 O H OCH.sub.3 ##STR155## H CH.sub.3 O H OCH.sub.3 (CH.sub.2).sub.3 CO.sub.2 CH.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CO.sub.2 C.sub.2 H.sub.5 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CF.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CH.sub.2 Cl H CH.sub.3 O H OCH.sub.3 CF.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CCl.sub.3 H CH.sub.3 O H OCH.sub.3 (CH.sub.2).sub.4 Cl H CH.sub.3 O H OCH.sub.3 (CH.sub.2).sub.3 Br H CH.sub.3 O H OCH.sub.3 CH.sub.2 CHCHCH.sub.2 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CHCH.sub.2 H CH.sub.3 O H CH.sub.3 O(CH.sub.2).sub.2 OCH.sub.3 H CH.sub.3 O H CH.sub.3 O(CH.sub.2).sub.3 OC.sub.2 H.sub.5 H CH.sub.3 O H CH.sub.3 O(CH.sub.2).sub.2 OCH(CH.sub.3).sub.2 H CH.sub.3 O H CH.sub.3 CH.sub.3 184-187(d) H CH.sub.3 O H CH.sub.3 OCH.sub.3 196-198(d) H CH.sub.3 O H OCH.sub.3 OCH.sub.3 192-195 H CH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 155-157 H CH(CH.sub.3).sub.2 O H CH.sub.3 OCH.sub.3 166-170 H CH(CH.sub.3).sub.2 O H OCH.sub.3 OCH.sub.3 176-177 __________________________________________________________________________

TABLE I-f __________________________________________________________________________ ##STR156## A' R.sup.I W R.sub.5 X Y m.p.(.degree.C.) __________________________________________________________________________ H CH.sub.3 O H CH.sub.3 Cl H CH.sub.3 O H H H H CH.sub.3 O H Cl Cl H CH.sub.3 O H OCH.sub.2 CH.sub.3 CH.sub.2 CH.sub.3 H CH.sub.3 O H CH.sub.3 CH(CH.sub.3).sub.2 H CH.sub.3 O H CH.sub.3 CH.sub.2 CH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.2 OCH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.3 CH.sub.2 OCH.sub.3 H CH.sub.3 O H CH.sub.3 (CH.sub.2).sub.4 OCH.sub.3 H CH.sub.3 O H CH.sub.3 (CH.sub.2).sub.2 OC.sub.2 H.sub.5 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CN H CH.sub.3 O H OCH.sub.3 ##STR157## H CH.sub.3 O H OCH.sub.3 (CH.sub.2).sub.3 CO.sub.2 CH.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CO.sub.2 C.sub.2 H.sub.5 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CF.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CH.sub.2 Cl H CH.sub.3 O H OCH.sub.3 CF.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CCl.sub.3 H CH.sub.3 O H OCH.sub.3 (CH.sub.2).sub.4 Cl H CH.sub.3 O H OCH.sub.3 (CH.sub.2).sub.3 Br H CH.sub.3 O H OCH.sub.3 CH.sub.2 CHCH.sub.2 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CHCHCH.sub.2 H CH.sub.3 O H CH.sub.3 O(CH.sub.2).sub.2 OCH.sub.3 H CH.sub.3 O H CH.sub.3 O(CH.sub.2).sub.3 OC.sub.2 H.sub.5 H CH.sub.3 O H CH.sub.3 O(CH.sub.2).sub.2 OCH(CH.sub. 3).sub.2 H CH.sub.3 O H CH.sub.3 CH.sub.3 165-175 H CH.sub.3 O H CH.sub.3 OCH.sub.3 170-72(d) H CH.sub.3 O H OCH.sub.3 OCH.sub.3 -- H CH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 158-160 H CH(CH.sub.3).sub.2 O H CH.sub.3 OCH.sub.3 106-111 H CH(CH.sub.3).sub.2 O H OCH.sub.3 OCH.sub.3 165-167 __________________________________________________________________________

TABLE I-g ______________________________________ ##STR158## m.p. A' R.sup.I W R.sub.5 X Y (.degree.C.) ______________________________________ H CH.sub.3 O H CH.sub.3 Cl H CH.sub.3 O H H H H CH.sub.3 O H Cl Cl H CH.sub.3 O H OCH.sub.2 CH.sub.3 CH.sub.2 CH.sub.3 H CH.sub.3 O H CH.sub.3 CH(CH.sub.3).sub.2 H CH.sub.3 O H CH.sub.3 CH.sub.2 CH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.2 OCH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.3 CH.sub.2 OCH.sub.3 H CH.sub.3 O H CH.sub.3 (CH.sub.2).sub.4 OCH.sub.3 H CH.sub.3 O H CH.sub.3 (CH.sub.2).sub.2 OC.sub.2 H.sub.5 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CN H CH.sub.3 O H OCH.sub.3 ##STR159## H CH.sub.3 O H OCH.sub.3 (CH.sub.2).sub.3 CO.sub.2 CH.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CO.sub.2 C.sub.2 H.sub.5 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CF.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CH.sub.2 Cl H CH.sub.3 O H OCH.sub.3 CF.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CCl.sub.3 H CH.sub.3 O H OCH.sub.3 (CH.sub.2).sub.4 Cl H CH.sub.3 O H OCH.sub.3 (CH.sub.2).sub.3 Br H CH.sub.3 O H OCH.sub.3 CH.sub.2 CHCH.sub.2 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CHCHCH.sub.2 H CH.sub.3 O H CH.sub.3 O(CH.sub.2).sub.2 OCH.sub.3 H CH.sub.3 O H CH.sub.3 O(CH.sub.2).sub.3 OC.sub.2 H.sub.5 H CH.sub.3 O H CH.sub.3 O(CH.sub.2).sub.2 OCH(CH.sub.3 ).sub.2 H CH.sub.3 O H CH.sub.3 CH.sub.3 194-196 H CH.sub.3 O H CH.sub.3 OCH.sub.3 162-165 H CH.sub.3 O H OCH.sub.3 OCH.sub.3 205-207 ______________________________________

TABLE I-h ______________________________________ ##STR160## m.p. A' R.sup.I W R.sub.5 X Y (.degree.C.) ______________________________________ H CH.sub.3 O H CH.sub.3 Cl H CH.sub.3 O H H H H CH.sub.3 O H Cl Cl H CH.sub.3 O H OCH.sub.2 CH.sub.3 CH.sub.2 CH.sub.3 H CH.sub.3 O H CH.sub.3 CH(CH.sub.3).sub.2 H CH.sub.3 O H CH.sub.3 CH.sub.2 CH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.2 OCH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.3 CH.sub.2 OCH.sub.3 H CH.sub.3 O H CH.sub.3 (CH.sub.2).sub.4 OCH.sub.3 H CH.sub.3 O H CH.sub.3 (CH.sub.2).sub.2 OC.sub.2 H.sub.5 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CN H CH.sub.3 O H OCH.sub.3 ##STR161## H CH.sub.3 O H OCH.sub.3 (CH.sub.2).sub.3 CO.sub.2 CH.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CO.sub.2 C.sub.2 H.sub.5 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CF.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CH.sub.2 Cl H CH.sub.3 O H OCH.sub.3 CF.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CCl.sub.3 H CH.sub.3 O H OCH.sub.3 (CH.sub.2).sub.4 Cl H CH.sub.3 O H OCH.sub.3 (CH.sub.2).sub.3 Br H CH.sub.3 O H OCH.sub.3 CH.sub.2 CHCH.sub.2 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CHCHCH.sub.2 H CH.sub.3 O H CH.sub.3 O(CH.sub.2).sub.2 OCH.sub.3 H CH.sub.3 O H CH.sub.3 O(CH.sub.2).sub.3 OC.sub.2 H.sub.5 H CH.sub.3 O H CH.sub.3 O(CH.sub.2).sub.2 OCH(CH.sub.3).sub.2 H CH.sub.3 O H OCH.sub.3 CH.sub.3 168-170 H CH.sub.3 O H OCH.sub.3 OCH.sub.3 164-167 ______________________________________

TABLE I-i ______________________________________ ##STR162## m.p. A' R.sup.I W R.sub.5 X Y (.degree.C.) ______________________________________ H CH.sub.3 O H CH.sub.3 Cl H CH.sub.3 O H H H H CH.sub.3 O H Cl Cl H CH.sub.3 O H OCH.sub.2 CH.sub.3 CH.sub.2 CH.sub.3 H CH.sub.3 O H CH.sub.3 CH(CH.sub.3).sub.2 H CH.sub.3 O H CH.sub.3 CH.sub.2 CH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.2 OCH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.3 CH.sub.2 OCH.sub.3 H CH.sub.3 O H CH.sub.3 (CH.sub.2).sub.4 OCH.sub.3 H CH.sub.3 O H CH.sub.3 (CH.sub.2).sub.2 OC.sub.2 H.sub.5 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CN H CH.sub.3 O H OCH.sub.3 ##STR163## H CH.sub.3 O H OCH.sub.3 (CH.sub.2).sub.3 CO.sub.2 CH.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CO.sub.2 C.sub.2 H.sub.5 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CF.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CH.sub.2 Cl H CH.sub.3 O H OCH.sub.3 CF.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CCl.sub.3 H CH.sub.3 O H OCH.sub.3 (CH.sub.2).sub.4 Cl H CH.sub.3 O H OCH.sub.3 (CH.sub.2).sub.3 Br H CH.sub.3 O H OCH.sub.3 CH.sub.2 CHCH.sub.2 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CHCHCH.sub.2 H CH.sub.3 O H CH.sub.3 O(CH.sub.2).sub.2 OCH.sub.3 H CH.sub.3 O H CH.sub.3 O(CH.sub.2).sub.3 OC.sub.2 H.sub.5 H CH.sub.3 O H CH.sub.3 O(CH.sub.2).sub.2 OCH(CH.sub. 3).sub.2 H CH.sub.3 O H CH.sub.3 CH.sub.3 189-190 H CH.sub.3 O H OCH.sub.3 CH.sub.3 189-190 H CH.sub.3 O H OCH.sub.3 OCH.sub.3 180-182 ______________________________________

TABLE I-j ______________________________________ ##STR164## m.p. A' R.sup.I W R.sub.5 X Y (.degree.C.) ______________________________________ H CH.sub.3 O H CH.sub.3 Cl H CH.sub.3 O H H H H CH.sub.3 O H Cl Cl H CH.sub.3 O H OCH.sub.2 CH.sub.3 CH.sub.2 CH.sub.3 H CH.sub.3 O H CH.sub.3 CH(CH.sub.3).sub.2 H CH.sub.3 O H CH.sub.3 CH.sub.2 CH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.2 OCH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.3 CH.sub.2 OCH.sub.3 H CH.sub.3 O H CH.sub.3 (CH.sub.2).sub. 4 OCH.sub.3 H CH.sub.3 O H CH.sub.3 (CH.sub.2).sub.2 OC.sub.2 H.sub.5 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CN H CH.sub.3 O H OCH.sub.3 ##STR165## H CH.sub.3 O H OCH.sub.3 (CH.sub.2).sub.3 CO.sub.2 CH.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CO.sub.2 C.sub.2 H.sub.5 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CF.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CH.sub.2 Cl H CH.sub.3 O H OCH.sub.3 CF.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CCl.sub.3 H CH.sub.3 O H OCH.sub.3 (CH.sub.2).sub.4 Cl H CH.sub.3 O H OCH.sub.3 (CH.sub.2).sub.3 Br H CH.sub.3 O H OCH.sub.3 CH.sub.2 CHCH.sub.2 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CHCHCH.sub.2 H CH.sub.3 O H CH.sub.3 O(CH.sub.2).sub.2 OCH.sub.3 H CH.sub.3 O H CH.sub.3 O(CH.sub.2).sub.3 OC.sub.2 H.sub.5 H CH.sub.3 O H CH.sub.3 O(CH.sub.2).sub.2 OCH(CH.sub.3).sub.2 H CH.sub.3 O H CH.sub.3 OCH.sub.3 160-163 H CH.sub.3 O H OCH.sub.3 OCH.sub.3 173-175 H CH.sub.3 O H CH.sub.3 CH.sub.3 174-176 ______________________________________

TABLE I-k ______________________________________ ##STR166## m.p. A' R.sup.I W R.sub.5 X Y (.degree.C.) ______________________________________ H CH.sub.3 O H CH.sub.3 Cl H CH.sub.3 O H H H H CH.sub.3 O H Cl Cl H CH.sub.3 O H OCH.sub.2 CH.sub.3 CH.sub.2 CH.sub.3 H CH.sub.3 O H CH.sub.3 CH(CH.sub.3).sub.2 H CH.sub.3 O H CH.sub.3 CH.sub.2 CH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.2 OCH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.3 CH.sub.2 OCH.sub.3 H CH.sub.3 O H CH.sub.3 (CH.sub.2).sub.4 OCH.sub.3 H CH.sub.3 O H CH.sub. 3 (CH.sub.2).sub.2 OC.sub.2 H.sub.5 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CN H CH.sub.3 O H OCH.sub.3 ##STR167## H CH.sub.3 O H OCH.sub.3 (CH.sub.2).sub.3 CO.sub.2 CH.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CO.sub.2 C.sub.2 H.sub.5 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CF.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CH.sub.2 Cl H CH.sub.3 O H OCH.sub.3 CF.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CCl.sub.3 H CH.sub.3 O H OCH.sub.3 (CH.sub.2).sub.4 Cl H CH.sub.3 O H OCH.sub.3 (CH.sub.2).sub.3 Br H CH.sub.3 O H OCH.sub.3 CH.sub.2 CHCH.sub.2 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CHCHCH.sub.2 H CH.sub.3 O H CH.sub.3 O(CH.sub.2).sub.2 OCH.sub.3 H CH.sub.3 O H CH.sub.3 O(CH.sub.2).sub.3 OC.sub.2 H.sub.5 H CH.sub.3 O H CH.sub.3 O(CH.sub.2).sub.2 OCH(CH.sub.3).sub.2 ______________________________________

TABLE I-l ______________________________________ ##STR168## m.p. A' R.sup.I W R.sub.5 X Y (.degree.C.) ______________________________________ H CH.sub.3 O H CH.sub.3 Cl H CH.sub.3 O H H H H CH.sub.3 O H Cl Cl H CH.sub.3 O H OCH.sub.2 CH.sub.3 CH.sub.2 CH.sub.3 H CH.sub.3 O H CH.sub.3 CH(CH.sub.3).sub.2 H CH.sub.3 O H CH.sub.3 CH.sub.2 CH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.2 OCH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.3 CH.sub.2 OCH.sub.3 H CH.sub.3 O H CH.sub.3 (CH.sub.2).sub.4 OCH.sub.3 H CH.sub.3 O H CH.sub. 3 (CH.sub.2).sub.2 OC.sub.2 H.sub.5 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CN H CH.sub.3 O H OCH.sub.3 ##STR169## H CH.sub.3 O H OCH.sub.3 (CH.sub.2).sub.3 CO.sub.2 CH.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CO.sub.2 C.sub.2 H.sub.5 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CF.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CH.sub.2 Cl H CH.sub.3 O H OCH.sub.3 CF.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CCl.sub.3 H CH.sub.3 O H OCH.sub.3 (CH.sub.2).sub.4 Cl H CH.sub.3 O H OCH.sub.3 (CH.sub.2).sub.3 Br H CH.sub.3 O H OCH.sub.3 CH.sub.2 CHCH.sub.2 H CH.sub.3 O H OCH.sub.3 CH.sub.2 CHCHCH.sub.2 H CH.sub.3 O H CH.sub.3 O(CH.sub.2).sub.2 OCH.sub.3 H CH.sub.3 O H CH.sub.3 O(CH.sub.2).sub.3 OC.sub.2 H.sub.5 H CH.sub.3 O H CH.sub.3 O(CH.sub.2).sub.2 OCH(CH.sub.3).sub.2 ______________________________________

TABLE II-a ______________________________________ ##STR170## A' R.sup.I W R.sub.5 X.sub.1 Y.sub.1 m.p.(.degree.C.) ______________________________________ H CH.sub.3 O H H H H CH.sub.3 O H H OCH.sub.3 H CH.sub.3 O H H CH.sub.3 H CH.sub.3 O H Cl H H CH.sub.3 O H Cl OCH.sub.3 H CH.sub.3 O H Cl CH.sub.3 H CH.sub.3 O H OCH.sub.3 H H CH.sub.3 O H OCH.sub.3 OCH.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.3 H CH.sub.3 O H OC.sub.2 H.sub.5 H H CH.sub.3 O H OC.sub.2 H.sub.5 OCH.sub.3 H CH.sub.3 O H OC.sub.2 H.sub.5 CH.sub.3 H CH.sub.3 O H CH.sub.3 H H CH.sub.3 O H CH.sub.3 OCH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.3 H CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-Cl CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-CH.sub.3 CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-Br CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-C.sub.2 H.sub.5 CH.sub.3 O H OCH.sub.3 OCH.sub.3 H CH(CH.sub.3).sub.2 O CH OCH.sub.3 OCH.sub.3 H CH.sub.2 CHCH.sub.2 O CH OCH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 CH.sub.3 H CH.sub.3 S H CH.sub.3 CH.sub.3 H CH.sub.3 S H OCH.sub.3 OCH.sub.3 H CH.sub.3 S H H H H CH(CH.sub.3).sub.2 S H CH.sub.3 CH.sub.3 ______________________________________

TABLE II-b ______________________________________ ##STR171## A' R.sup.I W R.sub.5 X.sub.1 Y.sub.1 m.p. (.degree.C.) ______________________________________ H CH.sub.3 O H H H H CH.sub.3 O H H OCH.sub.3 H CH.sub.3 O H H CH.sub.3 H CH.sub.3 O H Cl H H CH.sub.3 O H Cl OCH.sub.3 H CH.sub.3 O H Cl CH.sub.3 H CH.sub.3 O H OCH.sub.3 H H CH.sub.3 O H OCH.sub.3 OCH.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.3 H CH.sub.3 O H OC.sub.2 H.sub.5 H H CH.sub.3 O H OC.sub.2 H.sub.5 OCH.sub.3 H CH.sub.3 O H OC.sub.2 H.sub.5 CH.sub.3 H CH.sub.3 O H CH.sub.3 H H CH.sub.3 O H CH.sub.3 OCH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.3 H CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-Cl CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-CH.sub.3 CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-Br CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-C.sub.2 H.sub.5 CH.sub.3 O H OCH.sub.3 OCH.sub.3 H CH(CH.sub.3).sub.2 O CH OCH.sub.3 OCH.sub.3 H CH.sub.2 CHCH.sub.2 O CH OCH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 CH.sub.3 H CH.sub.3 S H CH.sub.3 CH.sub.3 H CH.sub.3 S H OCH.sub.3 OCH.sub.3 H CH.sub.3 S H H H H CH(CH.sub.3).sub.2 S H CH.sub.3 CH.sub.3 ______________________________________

TABLE II-c ______________________________________ ##STR172## A' R.sup.I W R.sub.5 X.sub.1 Y.sub.1 m.p. (.degree.C.) ______________________________________ H CH.sub.3 O H H H H CH.sub.3 O H H CH.sub.3 H CH.sub.3 O H Cl H H CH.sub.3 O H Cl OCH.sub.3 H CH.sub.3 O H Cl CH.sub.3 H CH.sub.3 O H OCH.sub.3 H H CH.sub.3 O H OCH.sub.3 OCH.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.3 H CH.sub.3 O H OC.sub.2 H.sub.5 H H CH.sub.3 O H OC.sub.2 H.sub.5 OCH.sub.3 H CH.sub.3 O H OC.sub.2 H.sub.5 CH.sub.3 H CH.sub.3 O H CH.sub.3 H H CH.sub.3 O H CH.sub.3 OCH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.3 129.degree. (d) H CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-Cl CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-CH.sub.3 CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-Br CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-C.sub.2 H.sub.5 CH.sub.3 O H OCH.sub.3 OCH.sub.3 H CH(CH.sub.3).sub.2 O CH OCH.sub.3 OCH.sub.3 H CH.sub.2 CHCH.sub.2 O CH OCH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 CH.sub.3 H CH.sub.3 S H CH.sub.3 CH.sub.3 H CH.sub.3 S H OCH.sub.3 OCH.sub.3 H CH.sub.3 S H H H H CH(CH.sub.3).sub.2 S H CH.sub.3 CH.sub.3 ______________________________________

TABLE II-d ______________________________________ ##STR173## A' R.sup.I W R.sub.5 X.sub.1 Y.sub.1 m.p. (.degree.C.) ______________________________________ H CH.sub.3 O H H H H CH.sub.3 O H H OCH.sub.3 H CH.sub.3 O H H CH.sub.3 H CH.sub.3 O H Cl H H CH.sub.3 O H Cl OCH.sub.3 H CH.sub.3 O H Cl CH.sub.3 H CH.sub.3 O H OCH.sub.3 H H CH.sub.3 O H OCH.sub.3 OCH.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.3 H CH.sub.3 O H OC.sub.2 H.sub.5 H H CH.sub.3 O H OC.sub.2 H.sub.5 OCH.sub.3 H CH.sub.3 O H OC.sub.2 H.sub.5 CH.sub.3 H CH.sub.3 O H CH.sub.3 H H CH.sub.3 O H CH.sub.3 OCH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.3 H CH.sub.3 O H OCH.sub.3 OCH.sub.3 126-133.degree. 5-Cl CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-CH.sub.3 CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-Br CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-C.sub.2 H.sub.5 CH.sub.3 O H OCH.sub.3 OCH.sub.3 H CH(CH.sub.3).sub.2 O CH OCH.sub.3 OCH.sub.3 H CH.sub.2 CHCH.sub.2 O CH OCH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 CH.sub.3 H CH.sub.3 S H CH.sub.3 CH.sub.3 H CH.sub.3 S H OCH.sub.3 OCH.sub.3 H CH.sub.3 S H H H H CH(CH.sub.3).sub.2 S H CH.sub.3 CH.sub.3 ______________________________________

TABLE II-e ______________________________________ ##STR174## A' R.sup.I W R.sub.5 X.sub.1 Y.sub.1 m.p. (.degree.C.) ______________________________________ H CH.sub.3 O H H H H CH.sub.3 O H H OCH.sub.3 H CH.sub.3 O H H CH.sub.3 H CH.sub.3 O H Cl H H CH.sub.3 O H Cl OCH.sub.3 H CH.sub.3 O H Cl CH.sub.3 H CH.sub.3 O H OCH.sub.3 H H CH.sub.3 O H OCH.sub.3 OCH.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.3 H CH.sub.3 O H OC.sub.2 H.sub.5 H H CH.sub.3 O H OC.sub.2 H.sub.5 OCH.sub.3 H CH.sub.3 O H OC.sub.2 H.sub.5 CH.sub.3 H CH.sub.3 O H CH.sub.3 H H CH.sub.3 O H CH.sub.3 OCH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.3 H CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-Cl CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-CH.sub.3 CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-Br CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-C.sub.2 H.sub.5 CH.sub.3 O H OCH.sub.3 OCH.sub.3 H CH(CH.sub.3).sub.2 O CH OCH.sub.3 OCH.sub.3 H CH.sub.2 CHCH.sub.2 O CH OCH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 CH.sub.3 H CH.sub.3 S H CH.sub.3 CH.sub.3 H CH.sub.3 S H OCH.sub.3 OCH.sub.3 H CH.sub.3 S H H H H CH(CH.sub.3).sub.2 S H CH.sub.3 CH.sub.3 ______________________________________

TABLE II-f ______________________________________ ##STR175## A' R.sup.I W R.sub.5 X.sub.1 Y.sub.1 m.p. (.degree.C.) ______________________________________ H CH.sub.3 O H H H H CH.sub.3 O H H OCH.sub.3 H CH.sub.3 O H H CH.sub.3 H CH.sub.3 O H Cl H H CH.sub.3 O H Cl OCH.sub.3 H CH.sub.3 O H Cl CH.sub.3 H CH.sub.3 O H OCH.sub.3 H H CH.sub.3 O H OCH.sub.3 OCH.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.3 H CH.sub.3 O H OC.sub.2 H.sub.5 H H CH.sub.3 O H OC.sub.2 H.sub.5 OCH.sub.3 H CH.sub.3 O H OC.sub.2 H.sub.5 CH.sub.3 H CH.sub.3 O H CH.sub.3 H H CH.sub.3 O H CH.sub.3 OCH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.3 H CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-Cl CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-CH.sub.3 CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-Br CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-C.sub.2 H.sub.5 CH.sub.3 O H OCH.sub.3 OCH.sub.3 H CH(CH.sub.3).sub.2 O CH OCH.sub.3 OCH.sub.3 H CH.sub.2 CHCH.sub.2 O CH OCH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 CH.sub.3 H CH.sub.3 S H CH.sub.3 CH.sub.3 H CH.sub.3 S H OCH.sub.3 OCH.sub.3 H CH.sub.3 S H H H H CH(CH.sub.3).sub.2 S H CH.sub.3 CH.sub.3 ______________________________________

TABLE II-g ______________________________________ ##STR176## A' R.sup.I W R.sub.5 X.sub.1 Y.sub.1 m.p. (.degree.C.) ______________________________________ H CH.sub.3 O H H H H CH.sub.3 O H H OCH.sub.3 H CH.sub.3 O H H CH.sub.3 H CH.sub.3 O H Cl H H CH.sub.3 O H Cl OCH.sub.3 H CH.sub.3 O H Cl CH.sub.3 H CH.sub.3 O H OCH.sub.3 H H CH.sub.3 O H OCH.sub.3 OCH.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.3 H CH.sub.3 O H OC.sub.2 H.sub.5 H H CH.sub.3 O H OC.sub.2 H.sub.5 OCH.sub.3 H CH.sub.3 O H OC.sub. 2 H.sub.5 CH.sub.3 H CH.sub.3 O H CH.sub.3 H H CH.sub.3 O H CH.sub.3 OCH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.3 H CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-Cl CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-CH.sub.3 CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-Br CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-C.sub.2 H.sub.5 CH.sub.3 O H OCH.sub.3 OCH.sub.3 H CH(CH.sub.3).sub.2 O CH OCH.sub.3 OCH.sub.3 H CH.sub.2 CHCH.sub.2 O CH OCH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 CH.sub.3 H CH.sub.3 S H CH.sub.3 CH.sub.3 H CH.sub.3 S H OCH.sub.3 OCH.sub.3 H CH.sub.3 S H H H H CH(CH.sub.3).sub.2 S H CH.sub.3 CH.sub.3 ______________________________________

TABLE II-h ______________________________________ ##STR177## A' R.sup.I W R.sub.5 X.sub.1 Y.sub.1 m.p. (.degree.C.) ______________________________________ H CH.sub.3 O H H H H CH.sub.3 O H H OCH.sub.3 H CH.sub.3 O H H CH.sub.3 H CH.sub.3 O H Cl H H CH.sub.3 O H Cl OCH.sub.3 H CH.sub.3 O H Cl CH.sub.3 H CH.sub.3 O H OCH.sub.3 H H CH.sub.3 O H OCH.sub.3 OCH.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.3 H CH.sub.3 O H OC.sub.2 H.sub.5 H H CH.sub.3 O H OC.sub.2 H.sub.5 OCH.sub.3 H CH.sub.3 O H OC.sub.2 H.sub.5 CH.sub.3 H CH.sub.3 O H CH.sub.3 H H CH.sub.3 O H CH.sub.3 OCH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.3 H CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-Cl CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-CH.sub.3 CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-Br CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-C.sub.2 H.sub.5 CH.sub.3 O H OCH.sub.3 OCH.sub.3 H CH(CH.sub.3).sub.2 O CH OCH.sub.3 OCH.sub.3 H CH.sub.2 CHCH.sub.2 O CH OCH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 CH.sub.3 H CH.sub.3 S H CH.sub.3 CH.sub.3 H CH.sub.3 S H OCH.sub.3 OCH.sub.3 H CH.sub.3 S H H H H CH(CH.sub.3).sub.2 S H CH.sub.3 CH.sub.3 ______________________________________

TABLE II-i ______________________________________ ##STR178## A' R.sup.I W R.sub.5 X.sub.1 Y.sub.1 m.p. (.degree.C.) ______________________________________ H CH.sub.3 O H H H H CH.sub.3 O H H OCH.sub.3 H CH.sub.3 O H H CH.sub.3 H CH.sub.3 O H Cl H H CH.sub.3 O H Cl OCH.sub.3 H CH.sub.3 O H Cl CH.sub.3 H CH.sub.3 O H OCH.sub.3 H H CH.sub.3 O H OCH.sub.3 OCH.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.3 H CH.sub.3 O H OC.sub.2 H.sub.5 H H CH.sub.3 O H OC.sub.2 H.sub.5 OCH.sub.3 H CH.sub.3 O H OC.sub.2 H.sub.5 CH.sub.3 H CH.sub.3 O H CH.sub.3 H H CH.sub.3 O H CH.sub.3 OCH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.3 H CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-Cl CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-CH.sub.3 CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-Br CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-C.sub.2 H.sub.5 CH.sub.3 O H OCH.sub.3 OCH.sub.3 H CH(CH.sub.3).sub.2 O CH OCH.sub.3 OCH.sub.3 H CH.sub.2 CHCH.sub.2 O CH OCH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 CH.sub.3 H CH.sub.3 S H CH.sub.3 CH.sub.3 H CH.sub.3 S H OCH.sub.3 OCH.sub.3 H CH.sub.3 S H H H H CH(CH.sub.3).sub.2 S H CH.sub.3 CH.sub.3 ______________________________________

TABLE II-j ______________________________________ ##STR179## A' R.sup.I W R.sub.5 X.sub.1 Y.sub.1 m.p. (.degree.C.) ______________________________________ H CH.sub.3 O H H H H CH.sub.3 O H H OCH.sub.3 H CH.sub.3 O H H CH.sub.3 H CH.sub.3 O H Cl H H CH.sub.3 O H Cl OCH.sub.3 H CH.sub.3 O H Cl CH.sub.3 H CH.sub.3 O H OCH.sub.3 H H CH.sub.3 O H OCH.sub.3 OCH.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.3 H CH.sub.3 O H OC.sub.2 H.sub.5 H H CH.sub.3 O H OC.sub.2 H.sub.5 OCH.sub.3 H CH.sub.3 O H OC.sub.2 H.sub.5 CH.sub. 3 H CH.sub.3 O H CH.sub.3 H H CH.sub.3 O H CH.sub.3 OCH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.3 H CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-Cl CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-CH.sub.3 CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-Br CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-C.sub.2 H.sub.5 CH.sub.3 O H OCH.sub.3 OCH.sub.3 H CH(CH.sub.3).sub.2 O CH OCH.sub.3 OCH.sub.3 H CH.sub.2 CHCH.sub.2 O CH OCH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 CH.sub.3 H CH.sub.3 S H CH.sub.3 CH.sub.3 H CH.sub.3 S H OCH.sub.3 OCH.sub.3 H CH.sub.3 S H H H H CH(CH.sub.3).sub.2 S H CH.sub.3 CH.sub.3 ______________________________________

TABLE II-k ______________________________________ ##STR180## A' R.sup.I W R.sub.5 X.sub.1 Y.sub.1 m.p. (.degree.C.) ______________________________________ H CH.sub.3 O H H H H CH.sub.3 O H H OCH.sub.3 H CH.sub.3 O H H CH.sub.3 H CH.sub.3 O H Cl H H CH.sub.3 O H Cl OCH.sub.3 H CH.sub.3 O H Cl CH.sub.3 H CH.sub.3 O H OCH.sub.3 H H CH.sub.3 O H OCH.sub.3 OCH.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.3 H CH.sub.3 O H OC.sub.2 H.sub.5 H H CH.sub.3 O H OC.sub.2 H.sub.5 OCH.sub.3 H CH.sub.3 O H OC.sub. 2 H.sub.5 CH.sub.3 H CH.sub.3 O H CH.sub.3 H H CH.sub.3 O H CH.sub.3 OCH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.3 H CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-Cl CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-Br CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-C.sub.2 H.sub.5 CH.sub.3 O H OCH.sub.3 OCH.sub.3 H CH(CH.sub.3).sub.2 O CH OCH.sub.3 OCH.sub.3 H CH.sub.2 CHCH.sub.2 O CH OCH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 CH.sub.3 H CH.sub.3 S H CH.sub.3 CH.sub.3 H CH.sub.3 S H OCH.sub.3 OCH.sub.3 H CH.sub.3 S H H H H CH(CH.sub.3).sub.2 S H CH.sub.3 CH.sub.3 ______________________________________

TABLE II-l ______________________________________ ##STR181## A' R.sup.I W R.sub.5 X.sub.1 Y.sub.1 m.p. (.degree.C.) ______________________________________ H CH.sub.3 O H H H H CH.sub.3 O H H OCH.sub.3 H CH.sub.3 O H H CH.sub.3 H CH.sub.3 O H Cl H H CH.sub.3 O H Cl OCH.sub.3 H CH.sub.3 O H Cl CH.sub.3 H CH.sub.3 O H OCH.sub.3 H H CH.sub.3 O H OCH.sub.3 OCH.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.3 H CH.sub.3 O H OC.sub.2 H.sub.5 H H CH.sub.3 O H OC.sub.2 H.sub.5 OCH.sub.3 H CH.sub.3 O H OC.sub.2 H.sub.5 CH.sub. 3 H CH.sub.3 O H CH.sub.3 H H CH.sub.3 O H CH.sub.3 OCH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.3 H CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-Cl CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-CH.sub.3 CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-Br CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-C.sub.2 H.sub.5 CH.sub.3 O H OCH.sub.3 OCH.sub.3 H CH(CH.sub.3).sub.2 O CH OCH.sub.3 OCH.sub.3 H CH.sub.2 CHCH.sub.2 O CH OCH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 CH.sub.3 H CH.sub.3 S H CH.sub.3 CH.sub.3 H CH.sub.3 S H OCH.sub.3 OCH.sub.3 H CH.sub.3 S H H H H CH(CH.sub.3).sub.2 S H CH.sub.3 CH.sub.3 ______________________________________

TABLE III-a ______________________________________ ##STR182## A' R.sup.I W R.sub.5 X.sub.11 Y.sub.1 m.p. (.degree.C.) ______________________________________ H CH.sub.3 O H CH.sub.2 H H CH.sub.3 O H CH.sub.2 OCH.sub.3 H CH.sub.3 O H CH.sub.2 CH.sub.3 H CH.sub.3 O H O H H CH.sub.3 O H O OCH.sub.3 H CH.sub.3 O H O CH.sub.3 5-CH.sub.3 CH.sub.3 O H O CH.sub.3 5-CH.sub.3 CH.sub.3 O H O CH.sub.3 5-Cl CH.sub.3 O H O CH.sub.3 5-Cl CH.sub.3 O H O CH.sub.3 H CH.sub.3 S H CH.sub.2 OCH.sub.3 H CH.sub.3 S H O CH.sub.3 H CH.sub.3 S H O CH.sub.3 H CH(CH.sub.3).sub.2 S H O CH.sub.3 H CH(CH.sub.3).sub.2 O H O CH.sub.3 H CH.sub.3 O CH.sub.3 O CH.sub.3 H CH(CH.sub.3).sub.2 O CH.sub.3 O CH.sub.3 ______________________________________

TABLE III-b ______________________________________ ##STR183## A' R.sup.I W R.sub.5 X.sub.11 Y.sub.1 m.p. (.degree.C.) ______________________________________ H CH.sub.3 O H CH.sub.2 H H CH.sub.3 O H CH.sub.2 OCH.sub.3 H CH.sub.3 O H CH.sub.2 CH.sub.3 H CH.sub.3 O H O H H CH.sub.3 O H O OCH.sub.3 H CH.sub.3 O H O CH.sub.3 147-155(d) 5-CH.sub.3 CH.sub.3 O H O CH.sub.3 5-CH.sub.3 CH.sub.3 O H O CH.sub.3 5-Cl CH.sub.3 O H O CH.sub.3 5-Cl CH.sub.3 O H O CH.sub.3 H CH.sub.3 S H CH.sub.2 OCH.sub.3 H CH.sub.3 S H O CH.sub.3 H CH.sub.3 S H O CH.sub.3 H CH(CH.sub.3).sub.2 S H O CH.sub.3 H CH(CH.sub.3).sub.2 O H O CH.sub.3 H CH.sub.3 O CH.sub.3 O CH.sub.3 H CH(CH.sub.3).sub.2 O CH.sub.3 O CH.sub.3 ______________________________________

TABLE III-c ______________________________________ ##STR184## A' R.sup.I W R.sub.5 X.sub.11 Y.sub.1 m.p. (.degree.C.) ______________________________________ H CH.sub.3 O H CH.sub.2 H H CH.sub.3 O H CH.sub.2 OCH.sub.3 H CH.sub.3 O H CH.sub.2 CH.sub.3 H CH.sub.3 O H O H H CH.sub.3 O H O OCH.sub.3 H CH.sub.3 O H O CH.sub.3 5-CH.sub.3 CH.sub.3 O H O CH.sub.3 5-CH.sub.3 CH.sub.3 O H O CH.sub.3 5-Cl CH.sub.3 O H O CH.sub.3 5-Cl CH.sub.3 O H O CH.sub.3 H CH.sub.3 S H CH.sub.2 OCH.sub.3 H CH.sub. 3 S H O CH.sub.3 H CH.sub.3 S H O CH.sub.3 H CH(CH.sub.3).sub.2 S H O CH.sub.3 H CH(CH.sub.3).sub.2 O H O CH.sub.3 H CH.sub.3 O CH.sub.3 O CH.sub.3 H CH(CH.sub.3).sub.2 O CH.sub.3 O CH.sub.3 ______________________________________

TABLE III-d ______________________________________ ##STR185## A' R.sup.I W R.sub.5 X.sub.11 Y.sub.1 m.p. (.degree.C.) ______________________________________ H CH.sub.3 O H CH.sub.2 H H CH.sub.3 O H CH.sub.2 OCH.sub.3 H CH.sub.3 O H CH.sub.2 CH.sub.3 H CH.sub.3 O H O H H CH.sub.3 O H O OCH.sub.3 H CH.sub.3 O H O CH.sub.3 180-182.degree. 5-CH.sub.3 O H O CH.sub.3 5-CH.sub.3 CH.sub.3 O H O CH.sub.3 5-Cl CH.sub.3 O H O CH.sub.3 5-Cl CH.sub.3 O H O CH.sub.3 H CH.sub.3 S H CH.sub.2 OCH.sub.3 H CH.sub.3 S H O CH.sub.3 H CH.sub.3 S H O CH.sub.3 H CH(CH.sub.3).sub.2 S H O CH.sub.3 H CH(CH.sub.3).sub.2 O H O CH.sub.3 H CH.sub.3 O CH.sub.3 O CH.sub.3 H CH(CH.sub.3).sub.2 O CH.sub.3 O CH.sub.3 ______________________________________

TABLE III-e ______________________________________ ##STR186## A' R.sup.I W R.sub.5 X.sub.11 Y.sub.1 m.p. (.degree.C.) ______________________________________ H CH.sub.3 O H CH.sub.2 H H CH.sub.3 O H CH.sub.2 OCH.sub.3 H CH.sub.3 O H CH.sub.2 CH.sub.3 H CH.sub.3 O H O H H CH.sub.3 O H O OCH.sub.3 H CH.sub.3 O H O CH.sub.3 175.degree.(d) 5-CH.sub.3 CH.sub.3 O H O CH.sub.3 5-CH.sub.3 CH.sub.3 O H O CH.sub.3 5-Cl CH.sub.3 O H O CH.sub.3 5-Cl CH.sub.3 O H O CH.sub.3 H CH.sub.3 S H CH.sub.2 OCH.sub.3 H CH.sub.3 S H O CH.sub.3 H CH.sub.3 S H O CH.sub.3 H CH(CH.sub.3).sub.2 S H O CH.sub.3 H CH(CH.sub.3).sub.2 O H O CH.sub.3 H CH.sub.3 O CH.sub.3 O CH.sub.3 H CH(CH.sub.3).sub.2 O CH.sub.3 O CH.sub.3 ______________________________________

TABLE III-f ______________________________________ ##STR187## A' R.sup.I W R.sub.5 X.sub.11 Y.sub.1 m.p. (.degree.C.) ______________________________________ H CH.sub.3 O H CH.sub.2 H H CH.sub.3 O H CH.sub.2 OCH.sub.3 H CH.sub.3 O H CH.sub.2 CH.sub.3 H CH.sub.3 O H O H H CH.sub.3 O H O OCH.sub.3 H CH.sub.3 O H O CH.sub.3 5-CH.sub.3 CH.sub.3 O H O CH.sub.3 5-CH.sub.3 CH.sub.3 O H O CH.sub.3 5-Cl CH.sub.3 O H O CH.sub.3 5-Cl CH.sub.3 O H O CH.sub.3 H CH.sub.3 S H CH.sub.2 OCH.sub.3 H CH.sub.3 S H O CH.sub.3 H CH.sub.3 S H O CH.sub.3 H CH(CH.sub.3).sub.2 S H O CH.sub.3 H CH(CH.sub.3).sub.2 O H O CH.sub.3 H CH.sub.3 O CH.sub.3 O CH.sub.3 H CH(CH.sub.3).sub.2 O CH.sub.3 O CH.sub.3 ______________________________________

TABLE IV-a ______________________________________ ##STR188## m.p. A' R.sup.I W R.sub.5 X Y (.degree.C.) ______________________________________ H CH.sub.3 O H CH.sub.3 CH.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.3 H CH.sub.3 O H OCH.sub.3 OCH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.2 OCH.sub.3 H CH.sub.3 O H OC.sub.2 H.sub.5 C.sub.2 H.sub.5 H CH.sub.3 S H OCH.sub.3 CH.sub.3 H CH.sub.3 S H CH.sub.3 CH.sub.3 H CH.sub.3 O CH.sub.3 CH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 OCH.sub.3 5-Cl CH.sub.3 O H OCH.sub. 3 OCH.sub.3 5-CH.sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 5-CH.sub.3 CH.sub.3 O H OCH.sub.3 OCH.sub.3 H C.sub.2 H.sub.5 O H OCH.sub.3 OCH.sub.3 H CH(CH.sub.3).sub.2 O H OCH.sub.3 OCH.sub.3 H CH.sub.2 CHCH.sub.2 O H OCH.sub.3 OCH.sub.3 ______________________________________

TABLE IV-b ______________________________________ ##STR189## m.p. A' R.sup.I W R.sub.5 X Y (.degree.C.) ______________________________________ H CH.sub.3 O H CH.sub.3 CH.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.3 H CH.sub.3 O H OCH.sub.3 OCH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.2 OCH.sub.3 H CH.sub.3 O H OC.sub.2 H.sub.5 C.sub.2 H.sub.5 H CH.sub.3 S H OCH.sub.3 CH.sub.3 H CH.sub.3 S H CH.sub.3 CH.sub.3 H CH.sub.3 O CH.sub.3 CH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 OCH.sub.3 5-Cl CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-CH.sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 5-CH.sub.3 CH.sub.3 O H OCH.sub.3 OCH.sub.3 H C.sub.2 H.sub.5 O H OCH.sub.3 OCH.sub.3 H CH(CH.sub.3).sub.2 O H OCH.sub.3 OCH.sub.3 H CH.sub.2 CHCH.sub.2 O H OCH.sub.3 OCH.sub.3 ______________________________________

TABLE IV-c ______________________________________ ##STR190## m.p. A' R.sup.I W R.sub.5 X Y (.degree.C.) ______________________________________ H CH.sub.3 O H CH.sub.3 CH.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.3 H CH.sub.3 O H OCH.sub.3 OCH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.2 OCH.sub.3 H CH.sub.3 O H OC.sub.2 H.sub.5 C.sub.2 H.sub.5 H CH.sub.3 S H OCH.sub.3 CH.sub.3 H CH.sub.3 S H CH.sub.3 CH.sub.3 H CH.sub.3 O CH.sub.3 CH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 OCH.sub.3 5-Cl CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-CH.sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 5-CH.sub.3 CH.sub.3 O H OCH.sub.3 OCH.sub.3 H C.sub.2 H.sub.5 O H OCH.sub.3 OCH.sub.3 H CH(CH.sub.3).sub.2 O H OCH.sub.3 OCH.sub.3 H CH.sub.2 CHCH.sub.2 O H OCH.sub.3 OCH.sub.3 ______________________________________

TABLE IV-d ______________________________________ ##STR191## m.p. A' R.sup.I W R.sub.5 X Y (.degree.C.) ______________________________________ H CH.sub.3 O H CH.sub.3 CH.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.3 H CH.sub.3 O H OCH.sub.3 OCH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.2 OCH.sub.3 H CH.sub.3 O H OC.sub.2 H.sub.5 C.sub.2 H.sub.5 H CH.sub.3 S H OCH.sub.3 CH.sub.3 H CH.sub.3 S H CH.sub.3 CH.sub.3 H CH.sub.3 O CH.sub.3 CH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 OCH.sub.3 5-Cl CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-CH.sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 5-CH.sub.3 CH.sub.3 O H OCH.sub.3 OCH.sub.3 H C.sub.2 H.sub.5 O H OCH.sub.3 OCH.sub.3 H CH(CH.sub.3).sub.2 O H OCH.sub.3 OCH.sub.3 H CH.sub.2 CHCH.sub.2 O H OCH.sub.3 OCH.sub.3 ______________________________________

TABLE IV-e ______________________________________ ##STR192## m.p. A' R.sup.I W R.sub.5 X Y (.degree.C.) ______________________________________ H CH.sub.3 O H CH.sub.3 CH.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.3 H CH.sub.3 O H OCH.sub.3 OCH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.2 OCH.sub.5 H CH.sub.3 O H OC.sub.2 H.sub.5 C.sub.2 H.sub.5 H CH.sub.3 S H OCH.sub.3 CH.sub.3 H CH.sub.3 S H CH.sub.3 CH.sub.3 H CH.sub.3 O CH.sub.3 CH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 OCH.sub.3 5-Cl CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-CH.sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 5-CH.sub.3 CH.sub.3 O H OCH.sub.3 OCH.sub.3 H C.sub.2 H.sub.5 O H OCH.sub.3 OCH.sub.3 H CH(CH.sub.3).sub.2 O H OCH.sub.3 OCH.sub.3 H CH.sub.2 CHCH.sub.2 O H OCH.sub.3 OCH.sub.3 ______________________________________

TABLE IV-f ______________________________________ ##STR193## m.p. A' R.sup.I W R.sub.5 X Y (.degree.C.) ______________________________________ H CH.sub.3 O H CH.sub.3 CH.sub.3 H CH.sub.3 O H OCH.sub.3 CH.sub.3 H CH.sub.3 O H OCH.sub.3 OCH.sub.3 H CH.sub.3 O H CH.sub.3 CH.sub.2 OCH.sub.3 H CH.sub.3 O H OC.sub.2 H.sub.5 C.sub.2 H.sub.5 H CH.sub.3 S H OCH.sub.3 CH.sub.3 H CH.sub.3 S H CH.sub.3 CH.sub.3 H CH.sub.3 O CH.sub.3 CH.sub.3 OCH.sub.3 H CH.sub.3 O CH.sub.3 OCH.sub.3 OCH.sub.3 5-Cl CH.sub.3 O H OCH.sub.3 OCH.sub.3 5-CH.sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 5-CH.sub.3 CH.sub.3 O H OCH.sub.3 OCH.sub.3 H C.sub.2 H.sub.5 O H OCH.sub.3 OCH.sub.3 H CH(CH.sub.3).sub.2 O H OCH.sub.3 OCH.sub.3 H CH.sub.2 CHCH.sub.2 O H OCH.sub.3 OCH.sub.3 ______________________________________

TABLE V ______________________________________ ##STR194## A' R.sup.I R.sub.5 X Y Z m.p. (.degree.C.) ______________________________________ H CH.sub.3 H CH.sub.3 CH.sub.3 CH H CH.sub.3 H CH.sub.3 OCH.sub.3 CH H CH.sub.3 H CH.sub.3 OC.sub.2 H.sub.5 CH H CH.sub.3 H OCH.sub.3 OCH.sub.3 CH H CH(CH.sub.3).sub.2 H OCH.sub.3 CH.sub.3 N H CH.sub.2 CH.sub.2 Cl H OCH.sub.3 OCH.sub.3 N H CH.sub.3 H CH.sub.3 CH.sub.3 N H CH.sub.3 H CH.sub.3 CH.sub.3 CCH.sub.3 H CH.sub.3 H CH.sub.3 OCH.sub.3 CCH.sub.3 ______________________________________


Adjustable valve for pipette gun Agent system
Air-fuel ratio detecting system Alcohol synthesis
Analog to digital converter Anti-skid brake system
Antibodies to plasmodium falciparum Antimicrobial toilet bars
Apparatus for analyzing biological specimens Apparatus for cleaning surfaces
Apparatus for collecting cultures Apparatus for mixing plastics
Apparatus for mounting advertisement notice Apparatus for performing work functions
Apparatus for sorting documents Apparatus for transporting bulk materials
Archery cross hair sight protector Arm exerciser
Asphalt heater Asynchronous pseudo SRAM
Athletic undergarment Attrition resistant catalysts
Automatic circuit board tester Automatic vehicle deceleration
Ball bearing Ball joint
Ball valve Barbed anchor pile
Benzimidazole derivatives with antihistaminic activity Biodegradable non-toxic gear oil
Block copolymer composition Body positioning device
Boolean gate definition Braking device particularly for skates
Brassiere Broad-band substrate-wave-coupled electro-optic modulator
Building element Built in board resistors
Calendar pad stand Caliper
Camera driving circuit Car cover and anchoring assembly
Car wash mop Catalyst for olefin polymerization
Cigarette smoking device Cleaving apparatus
Clock with constellation display Closure cap
Closure for telecommunications cable Coating Apparatus
Color temperature control circuit Combustor for waste gas treatment
Compact tailgate lifter Compound hair roller
Container venting arrangement Container with cover lockable thereon
Control for engine Conveyors system with volume sharing
Coordinate input device with display Core lifting chuck
Creeper Cuffed aircraft propeller
Cut-off gauge for saw tables Cycle lamp and attachment therefor
Cytomegalovirus proteinase Daunosamine nucleosides
Development system Device for eliminating malodorous smells
Device for mounting an item Differential hair curler
Digital audio tape recorder Digital camera
Digital video image splitter Direct station selection circuit
Dispensing device for radionuclide generators Disperse dyes
Display control device and method Divide-by-two frequency divider
Drilling device Drive circuit for resonant motors
Dynamic preloading of web pages Electric igniter assembly
Electric stapler Electrical cable connector
Electrical ground fault detection apparatus Electrically heatable catalytic converter insert
Emergency steering wheel braking system Enantiomeric resolution
Endarterectomy method and apparatus Engagement ring bracelet
Enhancing liquid jet erosion Exposure method
External flash control system Fabric conditioning compositions
Far infrared barbecue stove Fastening device
Fiber quality monitor Filter cleaning device
Fireplace heating unit Fishing rod holder
Flame-retardant nylon resin composition Flexible bag taping machine
Flexible lead chloride cathode construction Flow regulator
Flue for water heater Fluid diverting assembly
Fluorided composite catalyst Fragrance pro-accords
Freezer Frequency conversion system
Gas collecting apparatus Gas discharge laser
Gas-cleaning equipment and its use Gear box assembly
Generation of uniformly-distributed plasma Generator housing
Glass repair apparatus Golf grip training device
Golf training device Graphic display area classification
Heating apparatus for vehicle High density flash EPROM
High friction brake shoe assembly High voltage waveform generator
High-adhesion conductors High-power III-V semiconductor device
Hinge structure for automobile hoods HIV protease inhibitors
Hockey helmet with self-adjusting padding Increment/decrement sampling phase shifter
Induction heating apparatus Inflating device for use single-handed
Inflator/deflator accessory for air compressor Infusion devices and method
Inline dispersal valve Jaw assembly for endoscopic instruments
Ladder stabilizer Large amplitude sinusoidal voltammetry
LiClO.sub.4 Containing propellant compositions Light bulb changer
Liquid crystal display Liquid crystal display device
Liquid operated clock Load responsive valve assemblies
Locking mechanism for vending machines Low pressure transducer
Machines for classifying pharmaceutical capsules Magnetic sensor integrated with CMOS
Manchester pattern fault recognition Medical X-ray examination device
Method for reclaiming rubber Method of continuously wrapping products
Method of controlling reel drive Method of manufacturing three-dimensional compact
Method of producing copper-iron-aluminum catalysts Method of redrawing metal cup
Methods for vessel cannulation Mice lacking expression of osteoprotegerin
Microstrip wide band antenna Mobile floor crane
Mobile sound field correcting device Model rocket car
Modification of soy isolate Motor vehicle bumper
Motorcycle towing apparatus Mousse product
Multi-function pipe machining apparatus Multi-lug socket tool
Multi-size photoreceptor flange bearing Multi-story tower for goods display
Multifunctional bumper assembly Multilayer capacitor
Multiple reflection optical system Multiple stage hydrocarbon conversion process
Multiplex data communication system Multivalent antigen-binding proteins
N-Substituted alkynyl anilines Nanophase dental prosthetics and method
Navigational angle-measurement device Needle protector sheath
Net posts for ball games New organo-aluminum antiperspirant compositions
Nifedipine combination preparation Non-fouling print stylus
Oil funnel assembly Open back acoustic speaker module
Optical color printer assembly Optical device
Optical fiber decorative article Optical recording medium
Optimization of information bases Outdoor fan system
Panel lifter with antidrop protection Panels for constructing swimming pools
Penile implantation prosthesis Permanently lubricated bearing cartridge
Photo-induced DNA-cleaving agents Photographic composite board
Photosensitive material processing apparatus Pigment composition
PIM latch/extractor Pipeline identification
Piperazine derivatives Plant watering device
Plasma catalysis of carbon nanofibers Plasma gun with adjustable cathode
Plastic molded center tube assembly Poly-(-2-aminoalkyl)polyamines
Polyarylene sulfide molding composition Portable exercise machine
Portable eye examination system cart Powdered material parting agent
Power transmission Precision casting titanium aluminide
Preparation of substituted benzophenones Pressure swing adsorption process
Process for preparing .alpha.-ketocarboxylic acids Process for preparing 4-substituted imidazo[1,2-a]quinoxalines
Process for producing ammonium polythimolybdate Process for producing fluorinated catalysts
Process for producing pulse generator Process for purifying aminosulfenylcarbamate derivatives
Process for whitening kaolin Production of aqueous polymer compositions
Production of metallic powder Putting skill game
Radiation-sensitive resin composition Raster scanner variable-frequency clock circuit
Rattle-free door latch Regulated DC power supply
Repatterned integrated circuit chip package Retaining wall anchor system
Reversible door frame threshold Roof ventilator
Rotary adsorption/desorption gas treating apparatus Ruggedized tradesworkers radio
Safety harness Satellite communication routing arbitration techniques
Secure boot Self resonant scanning device
Semiconductor chip carrier system Semiconductor memory device
Sensor with improved drift stability Shaving apparatus
Shock absorber Shower head
Shutter device Simulated moving bed reaction process
Single barrel externally powdered gun Ski goggles
Slider window assembly Snap-fit-button
Socket-wrench removable oil filter Sod harvester
Solar control safety window Soldering method and soldering apparatus
Speed change device Staged anaerobic reactor
Steam generation apparatus and methods Stent pattern with figure-eights
Stitching assembly for selvedging machine Strand casting process
Structure for growing mushrooms Sunblocking polymers and their formulation
Surgical probe apparatus and system Swimming pool alarm
Synergistic germicidal compositions containing 3,5-dimethyl-4-chlorophenol System for network resource management
Tacky-surface animal repeller Tag pin
Tamburello Tape measure endpiece
Telephone keypad input technique Tent
Toilet tank flush control Toner and developer compositions
Tonometer transducer positioning system Torque transmitting apparatus
Transfer apparatus Transformer with superconducting windings
Transgenic model of heart failure Tree shear
Tricyclo[6.4.0.0.sup.2,7 ] dodecane-3,6-diphenyl-1,8,4,5-tetracarboxylic acid dianhydrides Triorganotin cyanometallate compounds
Trouble lamp Truck mounted load scale
Two-cycle engine Umbilical safety joint
Unfurled side impact air bag Universal joint prosthesis with cap
Urine control device Variable microwave cold/warm noise source
Variable resistor Vehicle disabling device
Vehicle propulsion system Vehicular alternating current dynamo
Vermicular expanded graphite composite material Vertical card file
Video pedobarograph system Wafer chamfering machine
Webbing wind-up force limiting apparatus Weighing and packing system
Welded austenitic steel pipe assembly Well perforating apparatus
Wine dispenser Work transport system


TABLE VI ______________________________________ ##STR195## m.p. A' R.sup.I WR.sup.IV X Y Z (.degree.C.) ______________________________________ H CH.sub.3 OCH.sub.3 CH.sub.3 CH.sub.3 N H CH.sub.3 OC.sub.2 H.sub.5 OCH.sub.3 CH.sub.3 N H CH.sub.3 OCH.sub.2 CHCH.sub.2 OCH.sub.3 CH.sub.3 N H CH.sub.3 OCH.sub.3 OCH.sub.3 CH.sub.3 CH H CH.sub.3 OCH.sub.3 CH.sub.3 CH.sub.3 CH H CH.sub.3 OCH(CH.sub.3).sub.2 CH.sub.3 CH.sub.3 CH H CH.sub.3 OC.sub.2 H.sub.5 CH.sub.3 CH.sub.3 CH H CH.sub.3 OCH.sub.3 CH.sub.3 CH.sub.3 CH H CH.sub.3 O(CH.sub.2).sub.3 CH.sub.3 CH.sub.3 CH.sub.3 CH H CH.sub.3 OCH.sub.2 CHCHCH.sub.3 CH.sub.3 CH.sub.3 CH H CH.sub.3 OC.sub.2 H.sub.5 CH.sub.3 CH.sub.3 CCH.sub.3 H CH.sub.3 SCH.sub.3 CH.sub.3 OCH.sub.3 N H CH.sub.3 SC.sub.2 H.sub.5 CH.sub.3 OCH.sub.3 N H CH.sub.3 SCH.sub.2 CHCH.sub.2 CH.sub.3 CH.sub.3 CH H CH.sub.3 S(CH.sub.2).sub.4 CH.sub.3 CH.sub.3 CH.sub.3 CH ______________________________________

TABLE VII-a __________________________________________________________________________ ##STR196## A' QR.sup.I W R.sub.5 X Y m.p. (.degree.C.) __________________________________________________________________________ H SCH.sub.3 O H CH.sub.3 OCH.sub.3 H SCH(CH.sub.3).sub.2 O H CH.sub.3 OCH.sub.3 ##STR197## O H CH.sub.3 OCH.sub.3 H ##STR198## O H CH.sub.3 OCH.sub.3 H SCH.sub.2 CHCH.sub.2 O H CH.sub.3 OCH.sub.3 H SCH.sub.2 CHCHC.sub.2 H.sub.5 O H CH.sub.3 OCH.sub.3 H SCH.sub.2CCC.sub.2 H.sub.5 O H CH.sub.3 OCH.sub.3 H S(CH.sub.2).sub.4 Cl O H CH.sub.3 OCH.sub.3 H SCH.sub.2 CN O H CH.sub.3 OCH.sub.3 5-Cl S(CH.sub.2).sub.2 OCH.sub.3 O H CH.sub.3 OCH.sub.3 5-Cl S(CH.sub.2).sub.4 OCH.sub.3 O H CH.sub.3 OCH.sub.3 5-CH.sub.3 SCH.sub.2 CHCHCH.sub.2 Cl O H CH.sub.3 OCH.sub.3 5-C.sub.2 H.sub.5 SCH.sub.2 CCCH.sub.2 CH.sub.2 Cl O H CH.sub.3 OCH.sub.3 H ##STR199## O H CH.sub.3 OCH.sub.3 H ##STR200## O H CH.sub.3 OCH.sub.3 H ##STR201## O H CH.sub.3 OCH.sub.3 H ##STR202## O H CH.sub.3 OCH.sub.3 H ##STR203## O H CH.sub.3 OCH.sub.3 H NH.sub.2 O H CH.sub.3 OCH.sub.3 H ##STR204## O H CH.sub.3 OCH.sub.3 H N(CH.sub.2 CN).sub.2 O H CH.sub.3 OCH.sub.3 H N(CH.sub.2 CH.sub.2 CN).sub.2 O H CH.sub.3 OCH.sub.3 H N(C.sub.2 H.sub.5).sub.2 O H CH.sub.3 OCH.sub.3 H ##STR205## O H CH.sub.3 OCH.sub.3 H N(CH.sub.2 CHCH.sub.2).sub.2 O H CH.sub.3 OCH.sub.3 5-Cl ##STR206## O H CH.sub.3 OCH.sub.3 5-Cl ##STR207## O H CH.sub.3 OCH.sub.3 5-Br NHCH.sub.3 O H CH.sub.3 CH.sub.3 5-CH.sub.3 NHC.sub.2 H.sub.5 O H CH.sub.3 CH.sub.3 5-CH.sub.3 NHCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H ##STR208## O H CH.sub.3 CH.sub.3 H NH(CH.sub.2).sub.5 CH.sub.3 O H CH.sub.3 CH.sub.3 H NH(CH.sub.2)OCH.sub.3 O H CH.sub.3 CH.sub.3 H NH(CH.sub.2).sub.3 OC.sub.2 H.sub.5 O H CH.sub. 3 CH.sub.3 H NH(CH.sub.2).sub.2 OCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H ##STR209## O H CH.sub.3 CH.sub.3 H NHCH.sub.2 CHCH.sub.2 O CH.sub.3 CH.sub.3 CH.sub.3 H NHCH.sub.2 CHCHC.sub.2 H.sub.5 O H CH.sub.3 CH.sub.3 H ##STR210## O H CH.sub.3 CH.sub.3 H ##STR211## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR212## O H CH.sub.3 CH.sub.3 H ##STR213## O H CH.sub.3 CH.sub.3 H ##STR214## O H CH.sub.3 CH.sub.3 H ##STR215## O H CH.sub.3 CH.sub.3 H ##STR216## O H CH.sub.3 CH.sub.3 H ##STR217## O H CH.sub.3 CH.sub.3 H ##STR218## O H CH.sub.3 CH.sub.3 H ##STR219## O H CH.sub.3 CH.sub.3 H ##STR220## O H CH.sub.3 CH.sub.3 H ##STR221## O H CH.sub.3 CH.sub.3 H ##STR222## O H CH.sub.3 OCH.sub.3 H ##STR223## O H CH.sub.3 OCH.sub.3 H ##STR224## O H CH.sub.3 OCH.sub.3 H ##STR225## O H CH.sub.3 OCH.sub.3 H ##STR226## O H CH.sub.3 OCH.sub.3 H ##STR227## O H CH.sub.3 OCH.sub.3 H ##STR228## O H CH.sub.3 OCH.sub.3 H ##STR229## O H CH.sub.3 OCH.sub.3 H ##STR230## O H CH.sub.3 CH.sub.3 H ##STR231## O H OCH.sub.3 CH.sub.3 H NHOC.sub.2 H.sub.5 O H OCH.sub.3 CH.sub.3 159-162 H N(CH.sub.3)OCH.sub.3 O H OCH.sub.3 OCH.sub.3 177-179(d) H N(CH.sub.3)OCH.sub.3 O H CH.sub.3 OCH.sub.3 180-182.5 H NHOCH.sub.3 O H CH.sub.3 CH.sub.3 172-174 H N(CH.sub.3)OCH.sub.3 O H CH.sub.3 CH.sub.3 150-154 H ##STR232## O H CH.sub.3 CH.sub.3 205-205.5 H ##STR233## O H CH.sub.3 CH.sub.3 167-170 H ##STR234## O H CH.sub.3 CH.sub.3 __________________________________________________________________________

TABLE VII-b ______________________________________ ##STR235## m.p. A' QR.sup.I W R.sub.5 X Y (.degree.C.) ______________________________________ H SCH.sub.3 O H CH.sub.3 OCH.sub.3 H SCH(CH.sub.3).sub.2 O H CH.sub.3 OCH.sub.3 ##STR236## O H CH.sub.3 OCH.sub.3 H ##STR237## O H CH.sub.3 OCH.sub.3 H SCH.sub.2 CHCH.sub.2 O H CH.sub.3 OCH.sub.3 H SCH.sub.2 CHCHC.sub.2 H.sub.5 O H CH.sub.3 OCH.sub.3 H SCH.sub.2CCC.sub.2 H.sub.5 O H CH.sub.3 OCH.sub.3 H S(CH.sub.2).sub.4 Cl O H CH.sub.3 OCH.sub.3 H SCH.sub.2 CN O H CH.sub.3 OCH.sub.3 5-Cl S(CH.sub.2).sub.2 OCH.sub.3 O H CH.sub.3 OCH.sub.3 5-Cl S(CH.sub.2).sub.4 OCH.sub.3 O H CH.sub.3 OCH.sub.3 5-CH.sub.3 SCH.sub.2 CHCHCH.sub.2 Cl O H CH.sub.3 OCH.sub.3 5-C.sub.2 H.sub.5 SCH.sub.2 CCCH.sub.2 CH.sub.2 Cl O H CH.sub.3 OCH.sub.3 H ##STR238## O H CH.sub.3 OCH.sub.3 H ##STR239## O H CH.sub.3 OCH.sub.3 H ##STR240## O H CH.sub.3 OCH.sub.3 H ##STR241## O H CH.sub.3 OCH.sub.3 H ##STR242## O H CH.sub.3 OCH.sub.3 H NH.sub.2 O H CH.sub.3 OCH.sub.3 H ##STR243## O H CH.sub.3 OCH.sub.3 H N(CH.sub.2 CN).sub.2 O H CH.sub.3 OCH.sub.3 H N(CH.sub.2 CH.sub.2 CN).sub.2 O H CH.sub.3 OCH.sub.3 H N(C.sub.2 H.sub.5).sub.2 O H CH.sub.3 OCH.sub.3 H ##STR244## O H CH.sub.3 OCH.sub.3 ______________________________________

TABLE VII-c ______________________________________ ##STR245## m.p. A' QR.sup.I W R.sub.5 X Y (.degree.C.) ______________________________________ H SCH.sub.3 O H CH.sub.3 OCH.sub.3 H SCH(CH.sub.3).sub.2 O H CH.sub.3 OCH.sub.3 ##STR246## O H CH.sub.3 OCH.sub.3 H ##STR247## O H CH.sub.3 OCH.sub.3 H SCH.sub.2 CHCH.sub.2 O H CH.sub.3 OCH.sub.3 H SCH.sub.2 CHCHC.sub.2 H.sub.5 O H CH.sub.3 OCH.sub.3 H SCH.sub.2C CC.sub.2 H.sub.5 O H CH.sub.3 OCH.sub.3 H S(CH.sub.2).sub.4 Cl O H CH.sub.3 OCH.sub.3 H SCH.sub.2 CN O H CH.sub.3 OCH.sub.3 5-Cl S(CH.sub.2).sub.2 OCH.sub.3 O H CH.sub.3 OCH.sub.3 5-Cl S(CH.sub.2).sub.4 OCH.sub.3 O H CH.sub.3 OCH.sub.3 5-CH.sub.3 SCH.sub.2 CHCHCH.sub.2 Cl O H CH.sub.3 OCH.sub.3 5-C.sub.2 H.sub.5 SCH.sub.2 CCCH.sub.2 CH.sub.2 Cl O H CH.sub.3 OCH.sub.3 H ##STR248## O H CH.sub.3 OCH.sub.3 H ##STR249## O H CH.sub.3 OCH.sub.3 H ##STR250## O H CH.sub.3 OCH.sub.3 H ##STR251## O H CH.sub.3 OCH.sub.3 H ##STR252## O H CH.sub.3 OCH.sub.3 H NH.sub.2 O H CH.sub.3 OCH.sub.3 H ##STR253## O H CH.sub.3 OCH.sub.3 H N(CH.sub.2 CN).sub.2 O H CH.sub.3 OCH.sub.3 H N(CH.sub.2 CH.sub.2 CN).sub.2 O H CH.sub.3 OCH.sub.3 H N(C.sub.2 H.sub.5).sub.2 O H CH.sub.3 OCH.sub.3 H ##STR254## O H CH.sub.3 OCH.sub.3 ______________________________________

TABLE VII-d __________________________________________________________________________ ##STR255## A' QR.sup.I W R.sub.5 X Y m.p. (.degree.C.) __________________________________________________________________________ H SCH.sub.3 O H CH.sub.3 OCH.sub.3 H SCH(CH.sub.3).sub.2 O H CH.sub.3 OCH.sub.3 ##STR256## O H CH.sub.3 OCH.sub.3 H ##STR257## O H CH.sub.3 OCH.sub.3 H SCH.sub.2 CHCH.sub.2 O H CH.sub.3 OCH.sub.3 H SCH.sub.2 CHCHC.sub.2 H.sub.5 O H CH.sub.3 OCH.sub.3 H SCH.sub.2C CC.sub.2 H.sub.5 O H CH.sub.3 OCH.sub.3 H S(CH.sub.2).sub.4 Cl O H CH.sub.3 OCH.sub.3 H SCH.sub.2 CN O H CH.sub.3 OCH.sub.3 5-Cl S(CH.sub.2).sub.2 OCH.sub.3 O H CH.sub.3 OCH.sub.3 5-Cl S(CH.sub.2).sub.4 OCH.sub.3 O H CH.sub.3 OCH.sub.3 5-CH.sub.3 SCH.sub.2 CHCHCH.sub.2 Cl O H CH.sub.3 OCH.sub.3 5-C.sub.2 H.sub.5 SCH.sub.2 CCCH.sub.2 CH.sub.2 Cl O H CH.sub.3 OCH.sub.3 H ##STR258## O H CH.sub.3 OCH.sub.3 H ##STR259## O H CH.sub.3 OCH.sub.3 H ##STR260## O H CH.sub.3 OCH.sub.3 H ##STR261## O H CH.sub.3 OCH.sub.3 H ##STR262## O H CH.sub.3 OCH.sub.3 H NH.sub.2 O H CH.sub.3 OCH.sub.3 H ##STR263## O H CH.sub.3 OCH.sub.3 H N(CH.sub.2 CN).sub.2 O H CH.sub.3 OCH.sub.3 H N(CH.sub.2 CH.sub.2 CN).sub.2 O H CH.sub.3 OCH.sub.3 H N(C.sub.2 H.sub.5).sub.2 O H CH.sub.3 OCH.sub.3 H ##STR264## O H CH.sub.3 OCH.sub.3 H ##STR265## O H CH.sub.3 OCH.sub.3 113-117.degree. __________________________________________________________________________

TABLE VII-e __________________________________________________________________________ ##STR266## A' QR.sup.I W R.sub.5 X Y m.p. (.degree.C.) __________________________________________________________________________ H SCH.sub.3 O H CH.sub.3 OCH.sub.3 H SCH(CH.sub.3).sub.2 O H CH.sub.3 OCH.sub.3 ##STR267## O H CH.sub.3 OCH.sub.3 H ##STR268## O H CH.sub.3 OCH.sub.3 H SCH.sub.2 CHCH.sub.2 O H CH.sub.3 OCH.sub.3 H SCH.sub.2 CHCHC.sub.2 H.sub.5 O H CH.sub.3 OCH.sub.3 H SCH.sub.2CCC.sub.2 H.sub.5 O H CH.sub.3 OCH.sub.3 H S(CH.sub.2).sub.4 Cl O H CH.sub.3 OCH.sub.3 H SCH.sub.2 CN O H CH.sub.3 OCH.sub.3 5-Cl S(CH.sub.2).sub.2 OCH.sub.3 O H CH.sub.3 OCH.sub.3 5-Cl S(CH.sub.2).sub.4 OCH.sub.3 O H CH.sub.3 OCH.sub.3 5-CH.sub.3 SCH.sub.2 CHCHCH.sub.2 Cl O H CH.sub.3 OCH.sub.3 5-C.sub.2 H.sub.5 SCH.sub.2 CCCH.sub.2 CH.sub.2 Cl O H CH.sub.3 OCH.sub.3 H ##STR269## O H CH.sub.3 OCH.sub.3 H ##STR270## O H CH.sub.3 OCH.sub.3 H ##STR271## O H CH.sub.3 OCH.sub.3 H ##STR272## O H CH.sub.3 OCH.sub.3 H ##STR273## O H CH.sub.3 OCH.sub.3 H NH.sub.2 O H CH.sub.3 OCH.sub.3 H ##STR274## O H CH.sub.3 OCH.sub. 3 H N(CH.sub.2 CN).sub.2 O H CH.sub.3 OCH.sub.3 H N(CH.sub.2 CH.sub.2 CN).sub.2 O H CH.sub.3 OCH.sub.3 H N(C.sub.2 H.sub.5).sub.2 O H CH.sub.3 OCH.sub.3 H ##STR275## O H CH.sub.3 OCH.sub.3 __________________________________________________________________________

TABLE VII-f __________________________________________________________________________ ##STR276## A' QR.sup.I W R.sub.5 X Y m.p. (.degree.C.) __________________________________________________________________________ H SCH.sub.3 O H CH.sub.3 OCH.sub.3 H SCH(CH.sub.3).sub.2 O H CH.sub.3 OCH.sub.3 ##STR277## O H CH.sub.3 OCH.sub.3 H ##STR278## O H CH.sub.3 OCH.sub.3 H SCH.sub.2 CHCH.sub.2 O H CH.sub.3 OCH.sub.3 H SCH.sub.2 CHCHC.sub.2 H.sub.5 O H CH.sub.3 OCH.sub.3 H SCH.sub.2CCC.sub.2 H.sub.5 O H CH.sub.3 OCH.sub.3 H S(CH.sub.2).sub. 4 Cl O H CH.sub.3 OCH.sub.3 H SCH.sub.2 CN O H CH.sub.3 OCH.sub.3 5-Cl S(CH.sub.2).sub.2 OCH.sub.3 O H CH.sub.3 OCH.sub.3 5-Cl S(CH.sub.2).sub.4 OCH.sub.3 O H CH.sub.3 OCH.sub.3 5-CH.sub.3 SCH.sub.2 CHCHCH.sub.2 Cl O H CH.sub.3 OCH.sub.3 5-C.sub.2 H.sub.5 SCH.sub.2 CCCH.sub.2 CH.sub.2 Cl O H CH.sub.3 OCH.sub.3 H ##STR279## O H CH.sub.3 OCH.sub.3 H ##STR280## O H CH.sub.3 OCH.sub.3 H ##STR281## O H CH.sub.3 OCH.sub.3 H ##STR282## O H CH.sub.3 OCH.sub.3 H ##STR283## O H CH.sub.3 OCH.sub.3 H NH.sub.2 O H CH.sub.3 OCH.sub.3 H ##STR284## O H CH.sub.3 OCH.sub.3 H N(CH.sub. 2 CN).sub.2 O H CH.sub.3 OCH.sub.3 H N(CH.sub.2 CH.sub.2 CN).sub.2 O H CH.sub.3 OCH.sub.3 H N(C.sub.2 H.sub.5).sub.2 O H CH.sub.3 OCH.sub.3 H ##STR285## O H CH.sub.3 OCH.sub.3 __________________________________________________________________________

TABLE VII-g __________________________________________________________________________ ##STR286## A' QR.sup.I W R.sub.5 X Y m.p. (.degree.C.) __________________________________________________________________________ H SCH.sub.3 O H CH.sub.3 OCH.sub.3 H SCH(CH.sub.3).sub.2 O H CH.sub.3 OCH.sub.3 ##STR287## O H CH.sub.3 OCH.sub.3 H ##STR288## O H CH.sub.3 OCH.sub.3 H SCH.sub.2 CHCH.sub.2 O H CH.sub.3 OCH.sub.3 H SCH.sub.2 CHCHC.sub.2 H.sub.5 O H CH.sub.3 OCH.sub.3 H SCH.sub.2CCC.sub.2 H.sub.5 O H CH.sub.3 OCH.sub.3 H S(CH.sub.2).sub.4 Cl O H CH.sub.3 OCH.sub.3 H SCH.sub.2 CN O H CH.sub.3 OCH.sub.3 5-Cl S(CH.sub.2).sub.2 OCH.sub.3 O H CH.sub.3 OCH.sub.3 5-Cl S(CH.sub.2).sub.4 OCH.sub.3 O H CH.sub.3 OCH.sub.3 5-CH.sub.3 SCH.sub.2 CHCHCH.sub.2 Cl O H CH.sub.3 OCH.sub.3 5-C.sub.2 H.sub.5 SCH.sub.2 CCCH.sub.2 CH.sub.2 Cl O H CH.sub.3 OCH.sub.3 H ##STR289## O H CH.sub.3 OCH.sub.3 H ##STR290## O H CH.sub.3 OCH.sub.3 H ##STR291## O H CH.sub.3 OCH.sub.3 H ##STR292## O H CH.sub.3 OCH.sub.3 H ##STR293## O H CH.sub.3 OCH.sub.3 H NH.sub.2 O H CH.sub.3 OCH.sub.3 H ##STR294## O H CH.sub.3 OCH.sub. 3 H N(CH.sub.2 CN).sub.2 O H CH.sub.3 OCH.sub.3 H N(CH.sub.2 CH.sub.2 CN).sub.2 O H CH.sub.3 OCH.sub.3 H N(C.sub.2 H.sub.5).sub.2 O H CH.sub.3 OCH.sub.3 H ##STR295## O H CH.sub.3 OCH.sub.3 __________________________________________________________________________

TABLE VII-h __________________________________________________________________________ ##STR296## A' QR.sup.I W R.sub.5 X Y m.p. (.degree.C.) __________________________________________________________________________ H SCH.sub.3 O H CH.sub.3 OCH.sub.3 H SCH(CH.sub.3).sub.2 O H CH.sub.3 OCH.sub.3 ##STR297## O H CH.sub.3 OCH.sub.3 H ##STR298## O H CH.sub.3 OCH.sub.3 H SCH.sub.2 CHCH.sub.2 O H CH.sub.3 OCH.sub.3 H SCH.sub.2 CHCHC.sub.2 H.sub.5 O H CH.sub.3 OCH.sub.3 H SCH.sub.2CCC.sub.2 H.sub.5 O H CH.sub.3 OCH.sub. 3 H S(CH.sub.2).sub.4 Cl O H CH.sub.3 OCH.sub.3 H SCH.sub.2 CN O H CH.sub.3 OCH.sub.3 5-Cl S(CH.sub.2).sub.2 OCH.sub.3 O H CH.sub.3 OCH.sub.3 5-Cl S(CH.sub.2).sub.4 OCH.sub.3 O H CH.sub.3 OCH.sub.3 5-CH.sub.3 SCH.sub.2 CHCHCH.sub.2 Cl O H CH.sub.3 OCH.sub.3 5-C.sub.2 H.sub.5 SCH.sub.2 CCCH.sub.2 CH.sub.2 Cl O H CH.sub.3 OCH.sub.3 H ##STR299## O H CH.sub.3 OCH.sub.3 H ##STR300## O H CH.sub.3 OCH.sub.3 H ##STR301## O H CH.sub.3 OCH.sub.3 H ##STR302## O H CH.sub.3 OCH.sub.3 H ##STR303## O H CH.sub.3 OCH.sub.3 H NH.sub.2 O H CH.sub.3 OCH.sub.3 H ##STR304## O H CH.sub.3 OCH.sub. 3 H N(CH.sub.2 CN).sub.2 O H CH.sub.3 OCH.sub.3 H N(CH.sub.2 CH.sub.2 CN).sub.2 O H CH.sub.3 OCH.sub.3 H N(C.sub.2 H.sub.5).sub.2 O H CH.sub.3 OCH.sub.3 H ##STR305## O H CH.sub.3 OCH.sub.3 __________________________________________________________________________

TABLE VII-i __________________________________________________________________________ ##STR306## A' QR.sup.I W R.sub.5 X Y m.p. (.degree.C.) __________________________________________________________________________ H SCH.sub.3 O H CH.sub.3 OCH.sub.3 H SCH(CH.sub.3).sub.2 O H CH.sub.3 OCH.sub.3 ##STR307## O H CH.sub.3 OCH.sub.3 H ##STR308## O H CH.sub.3 OCH.sub.3 H SCH.sub.2 CHCH.sub.2 O H CH.sub.3 OCH.sub.3 H SCH.sub.2 CHCHC.sub.2 H.sub.5 O H CH.sub.3 OCH.sub.3 H SCH.sub.2 CCC.sub.2 H.sub.5 O H CH.sub.3 OCH.sub.3 H S(CH.sub.2).sub.4 Cl O H CH.sub.3 OCH.sub.3 H SCH.sub.2 CN O H CH.sub.3 OCH.sub.3 5-Cl S(CH.sub.2).sub.2 OCH.sub.3 O H CH.sub.3 OCH.sub.3 5-Cl S(CH.sub.2).sub.4 OCH.sub.3 O H CH.sub.3 OCH.sub.3 5-CH.sub.3 SCH.sub.2 CHCHCH.sub.2 Cl O H CH.sub.3 OCH.sub.3 5-C.sub.2 H.sub.5 SCH.sub.2 CCCH.sub.2 CH.sub.2 Cl O H CH.sub.3 OCH.sub.3 H ##STR309## O H CH.sub.3 OCH.sub.3 H ##STR310## O H CH.sub.3 OCH.sub.3 H ##STR311## O H CH.sub.3 OCH.sub.3 H ##STR312## O H CH.sub.3 OCH.sub.3 H ##STR313## O H CH.sub.3 OCH.sub.3 H NH.sub.2 O H CH.sub.3 OCH.sub.3 H ##STR314## O H CH.sub.3 OCH.sub.3 H N(CH.sub.2 CN).sub.2 O H CH.sub.3 OCH.sub.3 H N(CH.sub.2 CH.sub.2 CN).sub.2 O H CH.sub.3 OCH.sub.3 H N(C.sub.2 H.sub.5).sub.2 O H CH.sub.3 OCH.sub.3 H ##STR315## O H CH.sub.3 OCH.sub.3 __________________________________________________________________________

TABLE VII-j ______________________________________ ##STR316## m.p. A' QR.sup.I W R.sub.5 X Y (.degree.C.) ______________________________________ H SCH.sub.3 O H CH.sub.3 OCH.sub.3 H SCH(CH.sub.3).sub.2 O H CH.sub.3 OCH.sub.3 ##STR317## O H CH.sub.3 OCH.sub.3 H ##STR318## O H CH.sub.3 OCH.sub.3 H SCH.sub.2 CHCH.sub.2 O H CH.sub.3 OCH.sub.3 H SCH.sub.2 CHCHC.sub.2 H.sub.5 O H CH.sub.3 OCH.sub.3 H SCH.sub.2C CC.sub.2 H.sub.5 O H CH.sub.3 OCH.sub.3 H S(CH.sub.2).sub.4 Cl O H CH.sub.3 OCH.sub.3 H SCH.sub.2 CN O H CH.sub.3 OCH.sub.3 5-Cl S(CH.sub.2).sub.2 OCH.sub.3 O H CH.sub.3 OCH.sub.3 5-Cl S(CH.sub.2).sub.4 OCH.sub.3 O H CH.sub.3 OCH.sub.3 5-CH.sub.3 SCH.sub.2 CHCHCH.sub.2 Cl O H CH.sub.3 OCH.sub.3 5-C.sub.2 H.sub.5 SCH.sub.2 CCCH.sub.2 CH.sub.2 Cl O H CH.sub.3 OCH.sub.3 H ##STR319## O H CH.sub.3 OCH.sub.3 H ##STR320## O H CH.sub.3 OCH.sub.3 H ##STR321## O H CH.sub.3 OCH.sub.3 H ##STR322## O H CH.sub.3 OCH.sub.3 H ##STR323## O H CH.sub.3 OCH.sub.3 H NH.sub.2 O H CH.sub.3 OCH.sub.3 H ##STR324## O H CH.sub.3 OCH.sub.3 H N(CH.sub.2 CN).sub.2 O H CH.sub.3 OCH.sub.3 H N(CH.sub.2 CH.sub.2 CN).sub.2 O H CH.sub.3 OCH.sub.3 H N(C.sub.2 H.sub.5).sub.2 O H CH.sub.3 OCH.sub.3 H ##STR325## O H CH.sub.3 OCH.sub.3 ______________________________________

TABLE VII-k ______________________________________ ##STR326## m.p. A' QR.sup.I W R.sub.5 X Y (.degree.C.) ______________________________________ H SCH.sub.3 O H CH.sub.3 OCH.sub.3 H SCH(CH.sub.3).sub.2 O H CH.sub.3 OCH.sub.3 ##STR327## O H CH.sub.3 OCH.sub.3 H ##STR328## O H CH.sub.3 OCH.sub.3 H SCH.sub.2 CHCH.sub.2 O H CH.sub.3 OCH.sub.3 H SCH.sub.2 CHCHC.sub.2 H.sub.5 O H CH.sub.3 OCH.sub.3 H SCH.sub.2CCC.sub.2 H.sub.5 O H CH.sub.3 OCH.sub.3 H S(CH.sub.2).sub.4 Cl O H CH.sub.3 OCH.sub.3 H SCH.sub.2 CN O H CH.sub.3 OCH.sub.3 5-Cl S(CH.sub.2).sub.2 OCH.sub.3 O H CH.sub.3 OCH.sub.3 5-Cl S(CH.sub.2).sub.4 OCH.sub.3 O H CH.sub.3 OCH.sub.3 5-CH.sub.3 SCH.sub.2 CHCHCH.sub.2 Cl O H CH.sub.3 OCH.sub.3 5-C.sub.2 H.sub.5 SCH.sub.2 CCCH.sub.2 CH.sub.2 Cl O H CH.sub.3 OCH.sub.3 H ##STR329## O H CH.sub.3 OCH.sub.3 H ##STR330## O H CH.sub.3 OCH.sub.3 H ##STR331## O H CH.sub.3 OCH.sub.3 H ##STR332## O H CH.sub.3 OCH.sub.3 H ##STR333## O H CH.sub.3 OCH.sub.3 H NH.sub.2 O H CH.sub.3 OCH.sub.3 H ##STR334## O H CH.sub.3 OCH.sub.3 H N(CH.sub.2 CN).sub.2 O H CH.sub.3 OCH.sub.3 H N(CH.sub.2 CH.sub.2 CN).sub.2 O H CH.sub.3 OCH.sub.3 H N(C.sub.2 H.sub.5).sub.2 O H CH.sub.3 OCH.sub.3 H ##STR335## O H CH.sub.3 OCH.sub.3 ______________________________________

TABLE VII-l ______________________________________ ##STR336## m.p. A' QR.sup.I W R.sub.5 X Y (.degree.C.) ______________________________________ H SCH.sub.3 O H CH.sub.3 OCH.sub.3 H SCH(CH.sub.3).sub.2 O H CH.sub.3 OCH.sub.3 ##STR337## O H CH.sub.3 OCH.sub.3 H ##STR338## O H CH.sub.3 OCH.sub.3 H SCH.sub.2 CHCH.sub.2 O H CH.sub.3 OCH.sub.3 H SCH.sub.2 CHCHC.sub.2 H.sub.5 O H CH.sub.3 OCH.sub.3 H SCH.sub.2CC C.sub.2 H.sub.5 O H CH.sub.3 OCH.sub.3 H S(CH.sub.2).sub.4 Cl O H CH.sub.3 OCH.sub.3 H SCH.sub.2 CN O H CH.sub.3 OCH.sub.3 5-Cl S(CH.sub.2).sub.2 OCH.sub.3 O H CH.sub.3 OCH.sub.3 5-Cl S(CH.sub.2).sub.4 OCH.sub.3 O H CH.sub.3 OCH.sub.3 5-CH.sub.3 SCH.sub.2 CHCHCH.sub.2 Cl O H CH.sub.3 OCH.sub.3 5-C.sub.2 H.sub.5 SCH.sub.2 CCCH.sub.2 CH.sub.2 Cl O H CH.sub.3 OCH.sub.3 H ##STR339## O H CH.sub.3 OCH.sub.3 H ##STR340## O H CH.sub.3 OCH.sub.3 H ##STR341## O H CH.sub.3 OCH.sub.3 H ##STR342## O H CH.sub.3 OCH.sub.3 H ##STR343## O H CH.sub.3 OCH.sub.3 H NH.sub.2 O H CH.sub.3 OCH.sub.3 H ##STR344## O H CH.sub.3 OCH.sub.3 H N(CH.sub.2 CN).sub.2 O H CH.sub.3 OCH.sub.3 H N(CH.sub.2 CH.sub.2 CN).sub.2 O H CH.sub.3 OCH.sub.3 H N(C.sub.2 H.sub.5).sub.2 O H CH.sub.3 OCH.sub.3 H ##STR345## O H CH.sub.3 OCH.sub.3 ______________________________________

TABLE VIII-a ______________________________________ ##STR346## A' QR.sup.I W R.sub.5 X.sub.1 Y.sub.1 m.p. (.degree.C.) ______________________________________ H SCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H SCH.sub.3 O H CH.sub.3 CH.sub.3 H SCH.sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H S(CH.sub.2).sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H NH(CH.sub.2).sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H NHCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H N(CH.sub.3).sub.2 O H OCH.sub.3 OCH.sub.3 H N(C.sub.2 H.sub.5).sub.2 O H OCH.sub.3 OCH.sub.3 ##STR347## O H OCH.sub.3 OCH.sub.3 H ##STR348## O H OCH.sub.3 OCH.sub.3 ______________________________________

TABLE VIII-b ______________________________________ ##STR349## A' QR.sup.I W R.sub.5 X.sub.1 Y.sub.1 m.p. (.degree.C.) ______________________________________ H SCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H SCH.sub.3 O H CH.sub.3 CH.sub.3 H SCH.sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H S(CH.sub.2).sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H NH(CH.sub.2).sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H NHCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H N(CH.sub.3).sub.2 O H OCH.sub.3 OCH.sub.3 H N(C.sub.2 H.sub.5).sub.2 O H OCH.sub.3 OCH.sub.3 ##STR350## O H OCH.sub.3 OCH.sub.3 H ##STR351## O H OCH.sub.3 OCH.sub.3 ______________________________________

TABLE VIII-c ______________________________________ ##STR352## A' QR.sup.I W R.sub.5 X.sub.1 Y.sub.1 m.p. (.degree.C.) ______________________________________ H SCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H SCH.sub.3 O H CH.sub.3 CH.sub.3 H SCH.sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H S(CH.sub.2).sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H NH(CH.sub.2).sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H NHCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H N(CH.sub.3).sub.2 O H OCH.sub.3 OCH.sub.3 H N(C.sub.2 H.sub.5).sub.2 O H OCH.sub.3 OCH.sub.3 ##STR353## O H OCH.sub.3 OCH.sub.3 H ##STR354## O H OCH.sub.3 OCH.sub.3 ______________________________________

TABLE VIII-d ______________________________________ ##STR355## A' QR.sup.I W R.sub.5 X.sub.1 Y.sub.1 m.p. (.degree.C.) ______________________________________ H SCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H SCH.sub.3 O H CH.sub.3 CH.sub.3 H SCH.sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H S(CH.sub.2).sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H NH(CH.sub.2).sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H NHCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H N(CH.sub.3).sub.2 O H OCH.sub.3 OCH.sub.3 H N(C.sub.2 H.sub.5).sub.2 O H OCH.sub.3 OCH.sub.3 ##STR356## O H OCH.sub.3 OCH.sub.3 H ##STR357## O H OCH.sub.3 OCH.sub.3 ______________________________________

TABLE VIII-e ______________________________________ ##STR358## A' QR.sup.I W R.sub.5 X.sub.1 Y.sub.1 m.p. (.degree.C.) ______________________________________ H SCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H SCH.sub.3 O H CH.sub.3 CH.sub.3 H SCH.sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H S(CH.sub.2).sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H NH(CH.sub.2).sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H NHCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H N(CH.sub.3).sub.2 O H OCH.sub.3 OCH.sub.3 H N(C.sub.2 H.sub.5).sub.2 O H OCH.sub.3 OCH.sub.3 ##STR359## O H OCH.sub.3 OCH.sub.3 H ##STR360## O H OCH.sub.3 OCH.sub.3 ______________________________________

TABLE VIII-f ______________________________________ ##STR361## A' QR.sup.I W R.sub.5 X.sub.1 Y.sub.1 m.p. (.degree.C.) ______________________________________ H SCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H SCH.sub.3 O H CH.sub.3 CH.sub.3 H SCH.sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H S(CH.sub.2).sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H NH(CH.sub.2).sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H NHCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H N(CH.sub.3).sub.2 O H OCH.sub.3 OCH.sub.3 H N(C.sub.2 H.sub.5).sub.2 O H OCH.sub.3 OCH.sub.3 ##STR362## O H OCH.sub.3 OCH.sub.3 H ##STR363## O H OCH.sub.3 OCH.sub.3 ______________________________________

TABLE VIII-g ______________________________________ ##STR364## A' QR.sup.I W R.sub.5 X.sub.1 Y.sub.1 m.p. (.degree.C.) ______________________________________ H SCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H SCH.sub.3 O H CH.sub.3 CH.sub.3 H SCH.sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H S(CH.sub.2).sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H NH(CH.sub.2).sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H NHCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H N(CH.sub.3).sub.2 O H OCH.sub.3 OCH.sub.3 H N(C.sub.2 H.sub.5).sub.2 O H OCH.sub.3 OCH.sub.3 ##STR365## O H OCH.sub.3 OCH.sub.3 H ##STR366## O H OCH.sub.3 OCH.sub.3 ______________________________________

TABLE VIII-h ______________________________________ ##STR367## A' QR.sup.I W R.sub.5 X.sub.1 Y.sub.1 m.p. (.degree.C.) ______________________________________ H SCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H SCH.sub.3 O H CH.sub.3 CH.sub.3 H SCH.sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H S(CH.sub.2).sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H NH(CH.sub.2).sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H NHCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H N(CH.sub.3).sub.2 O H OCH.sub.3 OCH.sub.3 H N(C.sub.2 H.sub.5).sub.2 O H OCH.sub.3 OCH.sub.3 ##STR368## O H OCH.sub. 3 OCH.sub.3 H ##STR369## O H OCH.sub.3 OCH.sub.3 ______________________________________

TABLE VIII-i ______________________________________ ##STR370## A' QR.sup.I W R.sub.5 X.sub.1 Y.sub.1 m.p. (.degree.C.) ______________________________________ H SCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H SCH.sub.3 O H CH.sub.3 CH.sub.3 H SCH.sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H S(CH.sub.2).sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H NH(CH.sub.2).sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H NHCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H N(CH.sub.3).sub.2 O H OCH.sub.3 OCH.sub.3 H N(C.sub.2 H.sub.5).sub.2 O H OCH.sub.3 OCH.sub.3 ##STR371## O H OCH.sub. 3 OCH.sub.3 H ##STR372## O H OCH.sub.3 OCH.sub.3 ______________________________________

TABLE VIII-j ______________________________________ ##STR373## A' QR.sup.I W R.sub.5 X.sub.1 Y.sub.1 m.p. (.degree.C.) ______________________________________ H SCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H SCH.sub.3 O H CH.sub.3 CH.sub.3 H SCH.sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H S(CH.sub.2).sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H NH(CH.sub.2).sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H NHCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H N(CH.sub.3).sub.2 O H OCH.sub.3 OCH.sub.3 H N(C.sub.2 H.sub.5).sub.2 O H OCH.sub.3 OCH.sub.3 ##STR374## O H OCH.sub.3 OCH.sub.3 H ##STR375## O H OCH.sub.3 OCH.sub.3 ______________________________________

TABLE VIII-k ______________________________________ ##STR376## A' QR.sup.I W R.sub.5 X.sub.1 Y.sub.1 m.p. (.degree.C.) ______________________________________ H SCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H SCH.sub.3 O H CH.sub.3 CH.sub.3 H SCH.sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H S(CH.sub.2).sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H NH(CH.sub.2).sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H NHCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H N(CH.sub.3).sub.2 O H OCH.sub.3 OCH.sub.3 H N(C.sub.2 H.sub.5).sub.2 O H OCH.sub.3 OCH.sub.3 ##STR377## O H OCH.sub. 3 OCH.sub.3 H ##STR378## O H OCH.sub.3 OCH.sub.3 ______________________________________

TABLE VIII-1 ______________________________________ ##STR379## A' QR.sup.I W R.sub.5 X.sub.1 Y.sub.1 m.p. (.degree.C.) ______________________________________ H SCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H SCH.sub.3 O H CH.sub.3 CH.sub.3 H SCH.sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H S(CH.sub.2).sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H NH(CH.sub.2).sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H NHCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H N(CH.sub.3).sub.2 O H OCH.sub.3 OCH.sub.3 H N(C.sub.2 H.sub.5).sub.2 O H OCH.sub.3 OCH.sub.3 ##STR380## O H OCH.sub.3 OCH.sub. 3 H ##STR381## O H OCH.sub.3 OCH.sub.3 ______________________________________

TABLE IX-a ______________________________________ ##STR382## A' QR.sup.I W R.sub.5 Y.sub.1 X.sub.11 m.p. (.degree.C.) ______________________________________ H SCH.sub.3 O H CH.sub.3 CH.sub.2 H SC.sub.2 H.sub.5 O H CH.sub.3 CH.sub.2 H SCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.2 H SCH.sub.2 CHCH.sub.2 O H CH.sub.3 CH.sub.2 H NHC.sub.2 H.sub.5 O H CH.sub.3 CH.sub.2 H NHCH(CH.sub.3).sub.2 O H CH.sub.3 O H NH(CH.sub.2).sub.5 CH.sub.3 O H CH.sub.3 O H NH(CH.sub.2).sub.8 CH.sub.3 O H CH.sub.3 O H N(CH.sub.3).sub.2 O H CH.sub.3 O ______________________________________

TABLE IX-b ______________________________________ ##STR383## A' QR.sup.I W R.sub.5 Y.sub.1 X.sub.11 m.p. (.degree.C.) ______________________________________ H SCH.sub.3 O H CH.sub.3 CH.sub.2 H SC.sub.2 H.sub.5 O H CH.sub.3 CH.sub.2 H SCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.2 H SCH.sub.2 CHCH.sub.2 O H CH.sub.3 CH.sub.2 H NHC.sub.2 H.sub.5 O H CH.sub.3 CH.sub.2 H NHCH(CH.sub.3).sub.2 O H CH.sub.3 O H NH(CH.sub.2).sub.5 CH.sub.3 O H CH.sub.3 O H NH(CH.sub.2).sub.8 CH.sub.3 O H CH.sub.3 O H N(CH.sub.3).sub.2 O H CH.sub.3 O ______________________________________

TABLE IX-c ______________________________________ ##STR384## A' QR.sup.I W R.sub.5 Y.sub.1 X.sub.11 m.p. (.degree.C.) ______________________________________ H SCH.sub.3 O H CH.sub.3 CH.sub.2 H SC.sub.2 H.sub.5 O H CH.sub.3 CH.sub.2 H SCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.2 H SCH.sub.2 CHCH.sub.2 O H CH.sub.3 CH.sub.2 H NHC.sub.2 H.sub.5 O H CH.sub.3 CH.sub.2 H NHCH(CH.sub.3).sub.2 O H CH.sub.3 O H NH(CH.sub.2).sub.5 CH.sub.3 O H CH.sub.3 O H NH(CH.sub.2).sub.8 CH.sub.3 O H CH.sub.3 O H N(CH.sub.3).sub.2 O H CH.sub.3 O ______________________________________

TABLE IX-d ______________________________________ ##STR385## A' QR.sup.I W R.sub.5 Y.sub.1 X.sub.11 m.p. (.degree.C.) ______________________________________ H SCH.sub.3 O H CH.sub.3 CH.sub.2 H SC.sub.2 H.sub.5 O H CH.sub.3 CH.sub.2 H SCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.2 H SCH.sub.2 CHCH.sub.2 O H CH.sub.3 CH.sub.2 H NHC.sub.2 H.sub.5 O H CH.sub.3 CH.sub.2 H NHCH(CH.sub.3).sub.2 O H CH.sub.3 O H NH(CH.sub.2).sub.5 CH.sub.3 O H CH.sub.3 O H NH(CH.sub.2).sub.8 CH.sub.3 O H CH.sub.3 O H N(CH.sub.3).sub.2 O H CH.sub.3 O ______________________________________

TABLE IX-e ______________________________________ ##STR386## A' QR.sup.I W R.sub.5 Y.sub.1 X.sub.11 m.p. (.degree.C.) ______________________________________ H SCH.sub.3 O H CH.sub.3 CH.sub.2 H SC.sub.2 H.sub.5 O H CH.sub.3 CH.sub.2 H SCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.2 H SCH.sub.2 CHCH.sub.2 O H CH.sub.3 CH.sub.2 H NHC.sub.2 H.sub.5 O H CH.sub.3 CH.sub.2 H NHCH(CH.sub.3).sub.2 O H CH.sub.3 O H NH(CH.sub.2).sub.5 CH.sub.3 O H CH.sub.3 O H NH(CH.sub.2).sub.8 CH.sub.3 O H CH.sub.3 O H N(CH.sub.3).sub.2 O H CH.sub.3 O ______________________________________

TABLE IX-f ______________________________________ ##STR387## A' QR.sup.I W R.sub.5 Y.sub.1 X.sub.11 m.p. (.degree.C.) ______________________________________ H SCH.sub.3 O H CH.sub.3 CH.sub.2 H SC.sub.2 H.sub.5 O H CH.sub.3 CH.sub.2 H SCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.2 H SCH.sub.2 CHCH.sub.2 O H CH.sub.3 CH.sub.2 H NHC.sub.2 H.sub.5 O H CH.sub.3 CH.sub.2 H NHCH(CH.sub.3).sub.2 O H CH.sub.3 O H NH(CH.sub.2).sub.5 CH.sub.3 O H CH.sub.3 O H NH(CH.sub.2).sub.8 CH.sub.3 O H CH.sub.3 O H N(CH.sub.3).sub.2 O H CH.sub.3 O ______________________________________

TABLE X-a ______________________________________ ##STR388## A' QR.sup.I W R.sub.5 X Y m.p. (.degree.C.) ______________________________________ H SCH.sub.3 O H CH.sub.3 CH.sub.3 H SC.sub.2 H.sub.5 O H CH.sub.3 CH.sub.3 H SCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H S(CH.sub.2).sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H SCH.sub.2 CHCH.sub.2 O H CH.sub.3 CH.sub.3 H S(CH.sub.2)CH.sub.3 O H CH.sub.3 CH.sub.3 H NHCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H NHC.sub.2 H.sub.5 O H CH.sub.3 CH.sub.3 H N(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H N(C.sub.2 H.sub.5 ).sub.2 O H CH.sub.3 CH.sub.3 ______________________________________

TABLE X-b ______________________________________ ##STR389## A' QR.sup.I W R.sub.5 X Y m.p. (.degree.C.) ______________________________________ H SCH.sub.3 O H CH.sub.3 CH.sub.3 H SC.sub.2 H.sub.5 O H CH.sub.3 CH.sub.3 H SCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H S(CH.sub.2).sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H SCH.sub.2 CHCH.sub.2 O H CH.sub.3 CH.sub.3 H S(CH.sub.2)CH.sub.3 O H CH.sub.3 CH.sub.3 H NHCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H NHC.sub.2 H.sub.5 O H CH.sub.3 CH.sub.3 H N(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H N(C.sub.2 H.sub.5 ).sub.2 O H CH.sub.3 CH.sub.3 ______________________________________

TABLE X-c ______________________________________ ##STR390## A' QR.sup.I W R.sub.5 X Y m.p. (.degree.C.) ______________________________________ H SCH.sub.3 O H CH.sub.3 CH.sub.3 H SC.sub.2 H.sub.5 O H CH.sub.3 CH.sub.3 H SCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H S(CH.sub.2).sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H SCH.sub.2 CHCH.sub.2 O H CH.sub.3 CH.sub.3 H S(CH.sub.2)CH.sub.3 O H CH.sub.3 CH.sub.3 H NHCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H NHC.sub.2 H.sub.5 O H CH.sub.3 CH.sub.3 H N(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H N(C.sub.2 H.sub.5).sub.2 O H CH.sub.3 CH.sub.3 ______________________________________

TABLE X-d ______________________________________ ##STR391## A' QR.sup.I W R.sub.5 X Y m.p. (.degree.C.) ______________________________________ H SCH.sub.3 O H CH.sub.3 CH.sub.3 H SC.sub.2 H.sub.5 O H CH.sub.3 CH.sub.3 H SCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H S(CH.sub.2).sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H SCH.sub.2 CHCH.sub.2 O H CH.sub.3 CH.sub.3 H S(CH.sub.2)CH.sub.3 O H CH.sub.3 CH.sub.3 H NHCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H NHC.sub.2 H.sub.5 O H CH.sub.3 CH.sub.3 H N(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H N(C.sub.2 H.sub. 5).sub.2 O H CH.sub.3 CH.sub.3 ______________________________________

TABLE X-e ______________________________________ ##STR392## A' QR.sup.I W R.sub.5 X Y m.p. (.degree.C.) ______________________________________ H SCH.sub.3 O H CH.sub.3 CH.sub.3 H SC.sub.2 H.sub.5 O H CH.sub.3 CH.sub.3 H SCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H S(CH.sub.2).sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H SCH.sub.2 CHCH.sub.2 O H CH.sub.3 CH.sub.3 H S(CH.sub.2)CH.sub.3 O H CH.sub.3 CH.sub.3 H NHCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H NHC.sub.2 H.sub.5 O H CH.sub.3 CH.sub.3 H N(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H N(C.sub.2 H.sub.5).sub.2 O H CH.sub.3 CH.sub.3 ______________________________________

TABLE X-f ______________________________________ ##STR393## A' QR.sup.I W R.sub.5 X Y m.p. (.degree.C.) ______________________________________ H SCH.sub.3 O H CH.sub.3 CH.sub.3 H SC.sub.2 H.sub.5 O H CH.sub.3 CH.sub.3 H SCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H S(CH.sub.2).sub.3 CH.sub.3 O H CH.sub.3 CH.sub.3 H SCH.sub.2 CHCH.sub.2 O H CH.sub.3 CH.sub.3 H S(CH.sub.2)CH.sub.3 O H CH.sub.3 CH.sub.3 H NHCH(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H NHC.sub.2 H.sub.5 O H CH.sub.3 CH.sub.3 H N(CH.sub.3).sub.2 O H CH.sub.3 CH.sub.3 H N(C.sub.2 H.sub.5).sub.2 O H CH.sub.3 CH.sub.3 ______________________________________

TABLE XI-a ______________________________________ ##STR394## A' ##STR395## W R.sub.5 X Y (.degree.C.)m.p. ______________________________________ ##STR396## O H CH.sub.3 CH.sub.3 H ##STR397## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR398## O H CH.sub.3 CH.sub.3 H ##STR399## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR400## O H CH.sub.3 CH.sub.3 H ##STR401## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR402## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR403## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR404## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR405## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR406## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR407## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR408## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR409## O H CH.sub.3 CH.sub.3 H ##STR410## O H CH.sub.3 CH.sub.3 H ##STR411## O H CH.sub.3 CH.sub.3 H ##STR412## O H CH.sub.3 CH.sub.3 H ##STR413## O H CH.sub.3 CH.sub.3 H ##STR414## O H CH.sub.3 CH.sub.3 H ##STR415## O H CH.sub.3 CH.sub.3 H ##STR416## O H CH.sub.3 CH.sub.3 H ##STR417## O H OCH.sub.3 OCH.sub.3 ______________________________________

TABLE XI-b ______________________________________ ##STR418## A' ##STR419## W R.sub.5 X Y (.degree. ______________________________________ C.)m.p. ##STR420## O H CH.sub.3 CH.sub.3 H ##STR421## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR422## O H CH.sub.3 CH.sub.3 H ##STR423## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR424## O H CH.sub.3 CH.sub.3 H ##STR425## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR426## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR427## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR428## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR429## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR430## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR431## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR432## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR433## O H CH.sub.3 CH.sub.3 H ##STR434## O H CH.sub.3 CH.sub.3 H ##STR435## O H CH.sub.3 OCH.sub.3 ______________________________________

TABLE XI-c ______________________________________ ##STR436## A' ##STR437## W R.sub.5 X Y (.degree. ______________________________________ C.)m.p. ##STR438## O H CH.sub.3 CH.sub.3 H ##STR439## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR440## O H CH.sub.3 CH.sub.3 H ##STR441## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR442## O H CH.sub.3 CH.sub.3 H ##STR443## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR444## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR445## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR446## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR447## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR448## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR449## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR450## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR451## O H CH.sub.3 CH.sub.3 H ##STR452## O H CH.sub.3 CH.sub.3 H ##STR453## O H CH.sub.3 OCH.sub.3 ______________________________________

TABLE XI-d ______________________________________ ##STR454## A' ##STR455## W R .sub.5 X Y (.degree. ______________________________________ C.)m.p. ##STR456## O H CH.sub.3 CH.sub.3 H ##STR457## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR458## O H CH.sub.3 CH.sub.3 H ##STR459## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR460## O H CH.sub.3 CH.sub.3 H ##STR461## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR462## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR463## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR464## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR465## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR466## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR467## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR468## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR469## O H CH.sub.3 CH.sub.3 H ##STR470## O H CH.sub.3 CH.sub.3 H ##STR471## O H CH.sub.3 OCH.sub.3 H ##STR472## O H CH.sub.3 CH.sub.3 155- 158.degree. ______________________________________

TABLE XI-e ______________________________________ ##STR473## A' ##STR474## W R.sub.5 X Y (.degree. ______________________________________ C.)m.p. ##STR475## O H CH.sub.3 CH.sub.3 H ##STR476## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR477## O H CH.sub.3 CH.sub.3 H ##STR478## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR479## O H CH.sub.3 CH.sub.3 H ##STR480## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR481## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR482## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR483## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR484## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR485## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR486## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR487## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR488## O H CH.sub.3 CH.sub.3 H ##STR489## O H CH.sub.3 CH.sub.3 H ##STR490## O H CH.sub.3 OCH.sub.3 ______________________________________

TABLE XI-f ______________________________________ ##STR491## A' ##STR492## W R.sub.5 X Y (.degree. ______________________________________ C.)m.p. ##STR493## O H CH.sub.3 CH.sub.3 H ##STR494## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR495## O H CH.sub.3 CH.sub.3 H ##STR496## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR497## O H CH.sub.3 CH.sub.3 H ##STR498## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR499## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR500## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR501## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR502## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR503## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR504## O CH.sub.3 CH.sub. 3 CH.sub.3 H ##STR505## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR506## O H CH.sub.3 CH.sub.3 H ##STR507## O H CH.sub.3 CH.sub.3 H ##STR508## O H CH.sub.3 OCH.sub.3 ______________________________________

TABLE XI-g ______________________________________ ##STR509## A' ##STR510## W R.sub.5 X Y (.degree. ______________________________________ C.)m.p. ##STR511## O H CH.sub.3 CH.sub.3 H ##STR512## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR513## O H CH.sub.3 CH.sub.3 H ##STR514## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR515## O H CH.sub.3 CH.sub.3 H ##STR516## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR517## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR518## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR519## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR520## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR521## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR522## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR523## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR524## O H CH.sub.3 CH.sub.3 H ##STR525## O H CH.sub.3 CH.sub.3 H ##STR526## O H OCH.sub.3 OCH.sub.3 ______________________________________

TABLE XI-h ______________________________________ ##STR527## A' ##STR528## W R.sub.5 X Y (.degree. ______________________________________ C.)m.p. ##STR529## O H CH.sub.3 CH.sub.3 H ##STR530## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR531## O H CH.sub.3 CH.sub.3 H ##STR532## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR533## O H CH.sub.3 CH.sub.3 H ##STR534## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR535## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR536## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR537## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR538## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR539## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR540## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR541## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR542## O H CH.sub.3 CH.sub.3 H ##STR543## O H CH.sub.3 CH.sub.3 H ##STR544## O H CH.sub.3 OCH.sub.3 ______________________________________

TABLE XI-i ______________________________________ ##STR545## A' ##STR546## W R.sub.5 X Y m.p. (.degree. ______________________________________ C.) ##STR547## O H CH.sub.3 CH.sub.3 H ##STR548## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR549## O H CH.sub.3 CH.sub.3 H ##STR550## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR551## O H CH.sub.3 CH.sub.3 H ##STR552## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR553## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR554## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR555## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR556## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR557## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR558## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR559## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR560## O H CH.sub.3 CH.sub.3 H ##STR561## O H CH.sub.3 CH.sub.3 H ##STR562## O H CH.sub.3 OCH.sub.3 ______________________________________

TABLE XI-j ______________________________________ ##STR563## A' ##STR564## W R.sub.5 X Y m.p. (.degree. ______________________________________ C.) ##STR565## O H CH.sub.3 CH.sub.3 H ##STR566## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR567## O H CH.sub.3 CH.sub.3 H ##STR568## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR569## O H CH.sub.3 CH.sub.3 H ##STR570## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR571## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR572## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR573## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR574## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR575## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR576## O CH.sub.3 CH.sub. 3 CH.sub.3 H ##STR577## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR578## O H CH.sub.3 CH.sub.3 H ##STR579## O H CH.sub.3 CH.sub.3 H ##STR580## O H CH.sub.3 OCH.sub.3 ______________________________________

TABLE XI-k ______________________________________ ##STR581## A' ##STR582## W R.sub.5 X Y m.p. (.degree. ______________________________________ C.) ##STR583## O H CH.sub.3 CH.sub.3 H ##STR584## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR585## O H CH.sub.3 CH.sub.3 H ##STR586## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR587## O H CH.sub.3 CH.sub.3 H ##STR588## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR589## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR590## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR591## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR592## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR593## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR594## O CH.sub.3 CH.sub. 3 CH.sub.3 H ##STR595## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR596## O H CH.sub.3 CH.sub.3 H ##STR597## O H CH.sub.3 CH.sub.3 H ##STR598## O H CH.sub.3 OCH.sub.3 ______________________________________

TABLE XI-1 ______________________________________ ##STR599## A' ##STR600## W R.sub.5 X Y m.p. (.degree.C.) ______________________________________ ##STR601## O H CH.sub.3 CH.sub.3 H ##STR602## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR603## O H CH.sub.3 CH.sub.3 H ##STR604## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR605## O H CH.sub.3 CH.sub.3 H ##STR606## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR607## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR608## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR609## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR610## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR611## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR612## O CH.sub.3 CH.sub.3 CH.sub.3 H ##STR613## 0 CH.sub.3 CH.sub.3 CH.sub.3 H ##STR614## O H CH.sub.3 CH.sub.3 H ##STR615## O H CH.sub.3 CH.sub.3 H ##STR616## O H CH.sub.3 OCH.sub.3 ______________________________________

TABLE XII ______________________________________ Other compounds within the scope of this invention include: ______________________________________ ##STR617## ##STR618## ##STR619## ##STR620## ##STR621## ##STR622## ##STR623## ##STR624## ##STR625## ##STR626## ##STR627## ##STR628## ##STR629## ##STR630## ##STR631## ##STR632## ##STR633## ______________________________________

TABLE XII-a ______________________________________ ##STR634## A' W' W R.sup.I ______________________________________ H S O C.sub.2 H.sub.5 H S O CH(CH.sub.3).sub.2 H S O CH.sub.2 CH.sub.2 Cl H S O (CH.sub.2).sub.6 H H S O ##STR635## H S O CH.sub.2CHCH.sub.2 H S O CH.sub.2CHCHCH.sub.3 H S O CH.sub.2 CHCHCH.sub.2 CH.sub.3 H S O ##STR636## H S O CH.sub.2 CH(CH.sub.3).sub.2 H S O CH.sub.2 CH(CH.sub.2 CH.sub.3).sub.2 H S O CH.sub.2 CH.sub.2 Cl H S O CH.sub.2 CH(CH.sub.2 Cl).sub.2 H S O CH.sub.2 CCl.sub.3 H S O (CH.sub.2).sub.6 Cl H S O (CH.sub.2).sub.6 Br H S O CH.sub. 2 CH.sub.2 Br H S O (CH.sub.2).sub.6 F H S O (CH.sub.2).sub.4 F H S O CH.sub.2 CN H S O CH.sub.2 CH.sub.2 CN H S O CH.sub.2 CH.sub.2 OCH.sub.3 H S O (CH.sub.2).sub.6 OCH.sub.3 H S O (CH.sub.2).sub.3 OCH.sub.3 H S O ##STR637## H S O ##STR638## H S O ##STR639## H S O ##STR640## H S O CH.sub.2 CN H S O ##STR641## H S O ##STR642## H S O ##STR643## H S O ##STR644## H S O ##STR645## H S O ##STR646## H S O ##STR647## H S O ##STR648## H S O CH.sub.2 OCH.sub.3 H S O CH.sub.2 OC.sub.2 H.sub.5 H S O CH.sub.2 O(CH.sub.2).sub.4 H H S O CH.sub.2 CHCHCl H S O CH.sub.2 CHCHCH.sub.2 Cl H S O CH.sub.2 CHCH(CH.sub.2).sub.3 Cl H S O CH.sub.2 CCCH.sub.3 H S O CH.sub.2 CCCH.sub.2 Cl H S O CH.sub.2 CCCH.sub.2 CH.sub.2Cl H S O ##STR649## H S O ##STR650## H S O ##STR651## H S O ##STR652## H S O ##STR653## H S O ##STR654## H S O ##STR655## H S O ##STR656## H S O ##STR657## H S O ##STR658## H S O ##STR659## H S O ##STR660## H S O ##STR661## H S O ##STR662## H S O ##STR663## H S O CH.sub.2 CH.sub.2 OCH.sub.2 CH.sub. 3 H S O CH.sub.2 CH.sub.2 OCH(CH.sub.3).sub.2 H S O ##STR664## H S O CH.sub.2 CH.sub.2 OCH.sub.2 CH.sub.2 Cl H S O CH.sub.2 CH.sub.2 OCH.sub.2 CCl.sub.3 H S O ##STR665## H S O ##STR666## H S O (CH.sub.2).sub.3 OCH(CH.sub.3).sub.2 H S O (CH.sub.2).sub.3 OCH.sub.2 CH.sub.3 H S O CH.sub.2 CH.sub.2 OCH.sub.2 CH.sub.2 OCH.sub.3 H S O CH.sub.2 CH.sub.2 (OCH.sub.2 CH.sub.2).sub.2 OC.sub.2 H.sub.5 5-CH.sub.3 S O CH.sub.3 H O O CH.sub.3 H S S CH.sub.3 4-CH.sub.3 S O CH.sub.3 4-Cl S O CH.sub.3 4-Br S O CH.sub.3 5-Br S O CH.sub.3 4-NO.sub.2 S O CH.sub.3 4-C.sub.2 H.sub.5 S O CH.sub.3 5-C.sub.2 H.sub.5 S O CH.sub.3 5-n-C.sub.7 H.sub. 9 S O CH.sub.3 5-CH(CH.sub.3).sub.2 S O CH.sub.3 4-CF.sub.3 S O CH.sub.3 5-OCH.sub.3 S O CH.sub.3 ______________________________________

TABLE XII-b ______________________________________ ##STR667## A' W' W R.sup.I ______________________________________ H S O C.sub.2 H.sub.5 H S O CH(CH.sub.3).sub.2 H S O CH.sub.2 CH.sub.2 Cl H S O (CH.sub.2).sub.6 H H S O ##STR668## H S O CH.sub.2CHCH.sub.2 H S O CH.sub.2CHCHCH.sub.3 H S O CH.sub.2 CHCHCH.sub.2 CH.sub.3 H S O ##STR669## H S O CH.sub.2 CH(CH.sub.3).sub.2 H S O CH.sub.2 CH(CH.sub.2 CH.sub.3).sub.2 H S O CH.sub.2 CH.sub.2 Cl H S O CH.sub.2 CH(CH.sub.2 Cl).sub.2 H S O CH.sub.2 CCl.sub.3 H S O (CH.sub.2).sub.6 Cl H S O (CH.sub.2).sub.6 Br H S O CH.sub.2 CH.sub.2 Br H S O (CH.sub.2).sub.6 F H S O (CH.sub.2).sub.4 F H S O CH.sub.2 CN H S O CH.sub.2 CH.sub.2 CN H S O CH.sub.2 CH.sub.2 OCH.sub.3 H S O (CH.sub.2).sub.6 OCH.sub.3 H S O (CH.sub.2).sub.3 OCH.sub.3 H S O ##STR670## H S O ##STR671## H S O ##STR672## H S O ##STR673## H S O CH.sub.2 CN H S O ##STR674## H S O ##STR675## H S O ##STR676## H S O ##STR677## H S O ##STR678## H S O ##STR679## H S O ##STR680## H S O ##STR681## H S O CH.sub.2 OCH.sub.3 H S O CH.sub.2 OC.sub.2 H.sub.5 H S O CH.sub.2 O(CH.sub.2).sub.4 H H S O CH.sub.2 CHCHCl H S O CH.sub.2 CHCHCH.sub.2 Cl H S O CH.sub.2 CHCH(CH.sub.2).sub.3 Cl H S O CH.sub.2 CCCH.sub.3 H S O CH.sub.2 CCCH.sub.2 Cl H S O CH.sub.2 CCCH.sub.2 CH.sub.2Cl H S O ##STR682## H S O ##STR683## H S O ##STR684## H S O ##STR685## H S O ##STR686## H S O ##STR687## H S O ##STR688## H S O ##STR689## H S O ##STR690## H S O ##STR691## H S O ##STR692## H S O ##STR693## H S O ##STR694## H S O ##STR695## H S O ##STR696## H S O CH.sub.2 CH.sub.2 OCH.sub.2 CH.sub.3 H S O CH.sub.2 CH.sub.2 OCH(CH.sub.3).sub.2 H S O ##STR697## H S O CH.sub.2 CH.sub.2 OCH.sub.2 CH.sub.2 Cl H S O CH.sub.2 CH.sub.2 OCH.sub.2 CCl.sub.3 H S O ##STR698## H S O ##STR699## H S O (CH.sub.2).sub.3 OCH(CH.sub.3).sub.2 H S O (CH.sub.2).sub.3 OCH.sub.2 CH.sub.3 H S O CH.sub.2 CH.sub.2 OCH.sub.2 CH.sub.2 OCH.sub.3 H S O CH.sub.2 CH.sub.2 (OCH.sub.2 CH.sub.2).sub.2 OC.sub.2 H.sub.5 5-CH.sub.3 S O CH.sub.3 H O O CH.sub.3 H S S CH.sub.3 2-CH.sub.3 S O CH.sub.3 2-Cl S O CH.sub.3 2-Br S O CH.sub.3 5-Br S O CH.sub.3 2-NO.sub.2 S O CH.sub.3 2-C.sub.2 H.sub.5 S O CH.sub.3 5-C.sub.2 H.sub.5 S O CH.sub.3 5-n-C.sub.7 H.sub.9 S O CH.sub.3 5-CH(CH.sub.3).sub. 2 S O CH.sub.3 2-CF.sub.3 S O CH.sub.3 5-OCH.sub.3 S O CH.sub.3 ______________________________________

TABLE XII-c ______________________________________ ##STR700## A' W' W R.sup.I ______________________________________ H S O C.sub.2 H.sub.5 H S O CH(CH.sub.3).sub.2 H S O CH.sub.2 CH.sub.2 Cl H S O (CH.sub.2).sub.6 H H S O ##STR701## H S O CH.sub.2CHCH.sub.2 H S O CH.sub.2CHCHCH.sub.3 H S O CH.sub.2 CHCHCH.sub.2 CH.sub.3 H S O ##STR702## H S O CH.sub.2 CH(CH.sub.3).sub.2 H S O CH.sub.2 CH(CH.sub.2 CH.sub.3).sub.2 H S O CH.sub.2 CH.sub.2 Cl H S O CH.sub.2 CH(CH.sub.2 Cl).sub.2 H S O CH.sub.2 CCl.sub.3 H S O (CH.sub.2).sub.6 Cl H S O (CH.sub.2).sub.6 Br H S O CH.sub.2 CH.sub.2 Br H S O (CH.sub.2).sub.6 F H S O (CH.sub.2).sub.4 F H S O CH.sub.2 CN H S O CH.sub.2 CH.sub.2 CN H S O CH.sub.2 CH.sub.2 OCH.sub.3 H S O (CH.sub.2).sub.6 OCH.sub.3 H S O (CH.sub.2).sub.3 OCH.sub.3 H S O ##STR703## H S O ##STR704## H S O ##STR705## H S O ##STR706## H S O CH.sub.2 CN H S O ##STR707## H S O ##STR708## H S O ##STR709## H S O ##STR710## H S O ##STR711## H S O ##STR712## H S O ##STR713## H S O ##STR714## H S O CH.sub.2 OCH.sub.3 H S O CH.sub.2 OC.sub.2 H.sub.5 H S O CH.sub.2 O(CH.sub.2).sub.4 H H S O CH.sub.2 CHCHCl H S O CH.sub.2 CHCHCH.sub.2 Cl H S O CH.sub.2 CHCH(CH.sub.2).sub.3 Cl H S O CH.sub.2 CCCH.sub.3 H S O CH.sub.2 CCCH.sub.2 Cl H S O CH.sub.2 CCCH.sub.2 CH.sub.2Cl H S O ##STR715## H S O ##STR716## H S O ##STR717## H S O ##STR718## H S O ##STR719## H S O ##STR720## H S O ##STR721## H S O ##STR722## H S O ##STR723## H S O ##STR724## H S O ##STR725## H S O ##STR726## H S O ##STR727## H S O ##STR728## H S O ##STR729## H S O CH.sub.2 CH.sub.2 OCH.sub.2 CH.sub.3 H S O CH.sub.2 CH.sub.2 OCH(CH.sub.3).sub.2 H S O ##STR730## H S O CH.sub.2 CH.sub.2 OCH.sub.2 CH.sub.2 Cl H S O CH.sub.2 CH.sub.2 OCH.sub.2 OCl.sub.3 H S O ##STR731## H S O ##STR732## H S O (CH.sub.2).sub.3 OCH(CH.sub.3).sub.2 H S O (CH.sub.2).sub.3 OCH.sub.2 CH.sub.3 H S O CH.sub.2 CH.sub.2 OCH.sub.2 CH.sub.2 OCH.sub.3 H S O CH.sub.2 CH.sub.2 (OCH.sub.2 CH.sub.2).sub.2 OC.sub.2 H.sub.5 5-CH.sub.3 S O CH.sub.3 H O O CH.sub.3 H S S CH.sub.3 4-CH.sub.3 S O CH.sub.3 4-Cl S O CH.sub.3 4-Br S O CH.sub.3 5-Br S O CH.sub.3 4-NO.sub.2 S O CH.sub.3 4-C.sub.2 H.sub.5 S O CH.sub.3 5-C.sub.2 H.sub.5 S O CH.sub.3 5-n-C.sub.7 H.sub.9 S O CH.sub.3 5-CH(CH.sub.3).sub. 2 S O CH.sub.3 4-CF.sub.3 S O CH.sub.3 5-OCH.sub.3 S O CH.sub.3 ______________________________________

TABLE XII-d ______________________________________ ##STR733## X Y m.p. (.degree.C.) ______________________________________ CH.sub.3 OCH.sub.3 182-187(d) OCH.sub.3 OCH.sub.3 195-197 ______________________________________



Formulations

Useful formulations of the compounds of Formula I can be prepared in conventional ways. They include dusts, granules, pellets, solutions, suspensions, emulsions, wettable powders, emulsifiable concentrates and the like. Many of these may be applied directly. Sprayable formulations can be extended in sutiable media and used at spray volumes of from a few liters to several hundred liters per hectare. High strength compositions are primarily used as intermediates for further formulation. The formulations, broadly, contain about 0.1% to 99% by weight of active ingredient(s) and at least one of (a) about 0.1% to 20% surfactant(s) and (b) about 1% to 99.9% solid or liquid diluent(s). More specifically, they will contain these ingredients in the following approximate proportions set forth in Table XVIII.

                  TABLE XVIII
    ______________________________________
                Active  Weight Percent*
                Ingred-           Surfac-
                ient    Diluent(s)
                                  tant(s)
    ______________________________________
    Wettable Powders
                  20-90      0-74     1-10
    Oil Suspensions,
                   3-50     40-95     0-15
    Emulsions, Solu-
    tions (including
    Emulsifiable
    Concentrates)
    Aqueous Suspension
                  10-50     40-84     1-20
    Dusts          1-25     70-99     0-5
    Granules and  0.1-95      5-99.9  0-15
    Pellets
    High Strength 90-99      0-10     0-2
    Compositions
    ______________________________________
     *Active ingredient plus at least one of a Surfactant or a Diluent equals
     100 weight percent.


Lower or higher levels of active ingredient can, of course, be present depending on the intended use and the physical properties of the compound. Higher ratios of surfactant to active ingredient are sometimes desirable, and are achieved by incorporation into the formulation or by tank mixing.

Typical solid diluents are described in Watkins, et al., "Handbook of Insecticide Dust Diluents and Carriers," 2nd Ed., Dorland Books, Caldwell, New Jersey, but other solids, either mined or manufactured, may be used. The more absorptive diluents are preferred for wettable powders and the denser ones for dusts. Typical liquid diluents and solvents are described in Marsden, "Solvents Guide," 2nd Ed., Interscience, New York, 1950. Solubility under 0.1% is preferred for suspension concentrates; solution concentrates are preferably stable against phase separation at 0.degree. C. "McCutcheon's Detergents and Emulsifiers Annual," MC Publishing Corp., Ridgewood, New Jersey, as well as Sisely and Wood, "Encyclopedia of Surface Active Agents," Chemical Publishing Co., Inc., New York 1964, list surfactants and recommended uses. All formulations can contain minor amounts of additives to reduce foaming, caking, corrosion, microbiological growth, etc.

The methods of making such compositions are well known. Solutions are prepared by simply mixing the ingredients. Fine solid compositions are made by blending and, usually grinding as in a hammer or fluid energy mill. Suspensions are prepared by wet milling (see, for example, Littler, U.S. Pat. No. 3,060,084). Granules and pellets may be made by spraying the active material upon preformed granular carriers or by agglomeration techniques. See J. E. Browning, "Agglomeration," Chemical Engineering, Dec. 4, 1967, pp. 147ff. and "Perry's Chemical Engineer's Handbook," 4th Ed., McGraw-Hill, New York, 1963, pp. 8-59ff.

For further information regarding the art of formulation, see for example:

H. M. Loux, U.S. Pat. No. 3,235,361, Feb. 15, 1966, Col. 6, line 16 through Col. 7, line 19 and Examples 10 through 41.

R. W. Luckenbaugh, U.S. Pat. No. 3,309,192, Mar. 14, 1967, Col. 5, line 43 through Col. 7, line 62 and Examples 8, 12, 15, 39, 41, 52, 53, 58, 132, 138-140, 162-164, 166, 167, 169-182.

H. Gysin and E. Knusli, U.S. Pat. No. 2,891,855, June 23, 1959, Col 3, line 66 through Col. 5, line 17 and Examples 1-4.

G. C. Klingman, "Weed Control as a Science", John Wiley & Sons, Inc. New York, 1961, pp. 81-96.

J. D. Fryer and S. A. Evans, "Weed Control Handbook", 5th Ed., Blackwell Scientific Publications, Oxford, 1968, pp. 101-103.

In the following examples all parts are by weight unless otherwise indicated.

EXAMPLE 7

    ______________________________________
    Wettable Powder
    ______________________________________
    methyl 3-[[(4,6-dimethylpyrimidin-2-yl)aminocarbonyl]-
                                80%
    aminosulfonyl]-2-thiophenecarboxylate
    sodium alkylnaphthalenesulfonate
                                2%
    sodium ligninsulfonate      2%
    synthetic amorphous silica  3%
    kaolinite                   13%
    ______________________________________


The ingredients are blended, hammer-milled until all the solids are essentially under 50 microns, reblended, and packaged.

EXAMPLE 8

    ______________________________________
    Wettable Powder
    ______________________________________
    methyl 3-[[(4,6-dimethoxypyrimidin-2-yl)-
                             50%
    aminocarbonyl]aminosulfonyl]-2-thiophene-
    carboxylate
    sodium alkylnaphthalenesulfonate
                              2%
    low viscosity methyl cellulose
                              2%
    diatomaceous earth       46%
    ______________________________________


The ingredients are blended, coarsely hammer-milled and then air-milled to produce particles essentially all below 10 microns in diameter. The product is reblended before packaging.

EXAMPLE 9

    ______________________________________
    Granule
    ______________________________________
    wettable powder of Example 8
                            5%
    attapulgite granules   95%
    (U.S.S. 20-40 mesh; 0.84-0.42 mm)
    ______________________________________


A slurry of wettable powder containing.apprxeq.25% solids is sprayed on the surface of attapulgite granules in a double-cone blender. The granules are dried and packaged.

EXAMPLE 10

    ______________________________________
    Extruded Pellet
    ______________________________________
    methyl 3-[[(4-methoxy-6-methylpyrimidin-2-yl)-
                                 25%
    aminocarbonyl]aminosulfonyl]-2-thiophenecarboxylate
    anhydrous sodium sulfate     10%
    crude calcium ligninsulfonate
                                  5%
    sodium alkylnaphthalenesulfonate
                                  1%
    calcium/magnesium bentonite  59%
    ______________________________________


The ingredients are blended, hammer-milled and then moistened about 12% water. The mixture is extruded as cylinders about 3 mm diameter which are cut to produce pellets about 3 mm long. These may be used directly after drying, or the dried pellets may be crushed to pass a U.S.S. No. 20 sieve (0.84 mm openings). The granules held on a U.S.S. No. 40 sieve (0.42 mm openings) may be packaged for use and the fines recycled.

EXAMPLE 11

    ______________________________________
    Oil Suspension
    ______________________________________
    methyl 3-[[(4,6-dimethylpyrimidin-2-yl)amino-
                               25%
    carbonyl]aminosulfonyl]-2-thiophenecarboxylate
    polyoxyethylene sorbitol hexaoleate
                                5%
    highly aliphatic hydrocarbon oil
                               70%
    ______________________________________


The ingredients are grounded together in a sand mill until the solid particles have been reduced to under about 5 microns. The resulting suspension may be applied directly, but preferably after being extended with oils or emulsified in water.

EXAMPLE 12

    ______________________________________
    Wettable Powder
    ______________________________________
    methyl 3-[[(4,6-dimethoxypyrimidin-2-yl)amino-
                               20%
    carbonyl]aminosulfonyl]-2-thiophenecarboxylate
    sodium alkylnaphthalenesulfonate
                               4%
    sodium ligninsulfonate     4%
    low viscosity methyl cellulose
                               3%
    attapulgite                69%
    ______________________________________


The ingredients are thoroughly blended. After grinding in a hammer mill to produce particles essentially all below 100 microns, the material is reblended and sifted through a U.S.S. No. 50 sieve (0.3 mm opening) and packaged.

EXAMPLE 13

    ______________________________________
    Oil Suspension
    ______________________________________
    methyl 3-[[(4-methoxy-6-methylpyrimidin-2-yl)-
                                 35%
    aminocarbonyl]aminosulfonyl]-2-thiophenecarboxylate
    blend of polyalcohol carboxylic
                                  6%
    esters and oil soluble petroleum
    sulfonates
    xylene                       59%
    ______________________________________


The ingredients are combined and ground together in a sand mill to produce particles essentially all below 3 microns. The product can be used directly, extended with oils, or emulsified in water.

EXAMPLE 14

    ______________________________________
    High Strength Concentrate
    ______________________________________
    methyl 3-[[(4,6-dimethylpyrimidin-2-yl)amino-
                                99%
    carbonyl]aminosulfonyl]-2-thiophenecarboxylate
    silica aerogel             0.5%
    synthetic amorphous silica 0.5%
    ______________________________________


The ingredients are blended and ground in a hammer mill to produce a material essentially all passing a U.S.S. No. 50 screen (0.3 mm opening). The concentrate may be formulated further if necessary.

EXAMPLE 15

    ______________________________________
    Low Strength Granule
    ______________________________________
    methyl 3-[[(4,6-dimethoxypyrimidin-2-yl)amino-
                               1%
    carbonyl]aminosulfonyl]-2-thiophenecarboxylate
    N,N--dimethylformamide     9%
    attapulgite granules       90%
    (U.S.S. 20-40 mesh)
    ______________________________________


The active ingredient is dissolved in the solvent and the solution is sprayed upon dedusted granules in a rotating blender. After spraying of the solution has been completed, the blender is allowed to run for a short period and then the granules are packaged.

EXAMPLE 16

    ______________________________________
    Aqueous Suspension
    ______________________________________
    methyl 3-[[(4-methoxy-6-methylpyrimidin-2-yl)-
                                 40%
    aminocarbonyl]aminosulfonyl]-2-thiophenecarboxylate
    polyacrylic acid thickener  0.3%
    dodecylphenol polyethylene glycol ether
                                0.5%
    disodium phosphate            1%
    monosodium phosphate        0.5%
    polyvinyl alcohol           1.0%
    water                       56.7%
    ______________________________________


The ingredients are blended and ground together in a sand mill to produce particles essentially all under 5 microns in size.

EXAMPLE 17

    ______________________________________
    Solution
    ______________________________________
    methyl 3-[[(4,6-dimethylpyrimidin-2-yl)amino-
                                5%
    carbonyl]aminosulfonyl]-2-thiophenecarboxylate
    water                      95%
    ______________________________________


The salt is added directly to the water with stirring to produce the solution, which may then be packaged for use.

EXAMPLE 18

    ______________________________________
    Granule
    ______________________________________
    methyl 3-[[(4,6-dimethoxypyrimidin-2-yl)amino-
                               80%
    carbonyl]aminosulfonyl]-2-thiophenecarboxylate
    wetting agent               1%
    crude ligninsulfonate salt (containing
                               10%
    5-20% of the natural sugars)
    attapulgite clay            9%
    ______________________________________


The ingredients are blended and milled to pass through a 100 mesh screen. This material is then added to a fluid bed granulator, the air flow is adjusted to gently fluidize the material, and a fine spray of water is sprayed onto the fluidized material. The fluidization and spraying are continued until granules of the desired size range are made. The spraying is stopped, but fluidization is continued, optionally with heat, until the water content is reduced to the desired level, generally less than 1%. The material is then discharged, screened to the desired size range, generally 14-100 mesh (1410-149 microns), and packaged for use.

EXAMPLE 19

    ______________________________________
    Low Strength Granule
    ______________________________________
    methyl 3-[[(4-methoxy-6-methylpyrimidin-2-yl)-
                                 0.1%
    aminocarbonyl]aminosulfonyl]-2-thiophenecarboxylate
    attapulgite granules        99.9%
    (U.S.S. 20-40 mesh)
    ______________________________________


The active ingredient is dissolved in a solvent and the solution is sprayed upon dedusted granules in a double cone blender. After spraying of the solution has been completed, the material is warmed to evaporate the slovent. The material is allowed to cool and then packaged.

UTILITY

The compounds of the present invention are powerful herbicides. They have utility for broad-spectrum pre- and/or post-emergence weed control in areas where complete control of all vegetation is desired, such as around fuel storage tanks, ammunition depots, industrial storage areas, parking lots, drive-in theaters, around billboards, highway and railroad structures. Alternatively, the subject compounds are useful for the selective pre- or post-emergence weed control in crops, such as wheat and soybeans.

The rates of application for the compounds of the invention are determined by a number of factors, including their use as selective or general herbicides, the crop species involved, the types of weeds to be controlled, wheather and climate, formulations selected, mode of application, amount of foliage present, etc. In general terms, the subject compounds should be applied at levels of around 0.06 to 10 kg/ha, the lower rates being suggested for use on lighter soils and/or those having a low organic matter content, for selective weed control or for situations where only short-term persistence is required.

The compounds of the invention may be used in combination with any other commercial herbicide examples of which are those of the triazine, triazole, uracil, urea, amide, diphenylether, carbamate and bipyridylium types.

The herbicidal properties of the subject compounds were discovered in a number of greenhouse tests. The test procedures are results follow.

TEST A

Seeds of crabgrass (Digitaria spp.), barnyardgrass (Enchinochloa crusgalli), wild oats (Avena fatua), Cassia tora, morningglory (Ipomoea spp.), cocklebur (Xanthium spp.), sorghum, corn, soybean, rice, wheat as well as nutsedge tubers were planted in a growth medium and treated preemergence with the chemicals dissolved in a non-phytotoxic solvent. At the same time, cotton having five leaves (including cotyledonary ones), bush beans with the third trifoliate leaf expanding, crabgrass, barnyardgrass and wild oats with two leaves, cassia with three leaves (including cotyledonary ones), morningglory and cocklebur with four leaves (including the cotyledonary ones), sorghum and corn with four leaves, soybean with two cotyledonary leaves, rice with three leaves, wheat with one leaf, and nutsedge with three-five leaves were sprayed. Treated plants and controls were maintained in a greenhouse for sixteen days, whereupon all species were compared to controls and visually rated for response to treatment. The ratings are based on a numerical scale extending from 0=no injury, to 10=complete kill. The accompanying descriptive symbols have the following meanings: B=burn; G=growth retardation; C=chlorosis/necrosis; D=defoliation; 6Y=abscised buds or flowers; 6F=delayed flowering; U=unusual pigmentation; S=albinism; E=emergence inhibition; and H=formative effects. The ratings for the compounds tested by this procedure are presented in Table A. It will be seen that certain of the compounds tested have utility for selective pre- and post-emergence weed control in soybean and wheat.

    TABLE A
         MORN-     BARN-        BUSH- COT- ING- COCKLE-  NUT- CRAB- YARD-
     WILD   SOY-  SOR- kg/ha BEAN TON GLORY BUR CASSIA SEDGE GRASS GRASS OATS
     WHEAT CORN BEAN RICE GHUM
       POST-EMERGENCE
      ##STR734##
      0.1 6C,9G,6Y 3U,9G 9C 5C,9G 0 5C,9G 5C,9G 6C,9G 2G 1C,9G 1C,9H 3G 2C,9G
     1C,9G
      ##STR735##
      0.1 5C,8G,6Y 7C,9G 10C 9C 2C 1C,9G 3C,8G 9C 1C,7G 2C,8G 2U,9G 5C,9G
     5C,9G 5U,9G
      ##STR736##
      0.1 8D,9G,6Y 7C,9G 10C 3C,9G 1C,3G 4C,9G 6C,9G 9C 2C,8G 3C,7G 1C,9G
     2C,8G 3C,9G 3C,9G
      ##STR737##
      0.1 9C 3C,7G 5C,8G 10C 1C 0 1C,5G 2C,8H 0 0 2C,8H 1C,2H -- 1C,9G
      ##STR738##
      0.4 6C,9G 3C,3H 1C,3H 1C,5G 2C,2H 1C 4G 2C,5H 0 0 2C,7H 2C,3G 1C,5G
     2C,9H
      ##STR739##
      0.1 2C,8G,6Y 9C 10C 10C 2C,7H 1C 1C 2C,9H 1H 1H 9H 5C,9G 2C,8G 2C,7H
      ##STR740##
      0.1 9C 9C 10C 6C 1C 1C 3C 10C 0 0 7C 2C 5C 9G
      ##STR741##
      0.4 3C,4G,6F 1C,7G 10C 10C 0 5C,5G 10C 10C 2C,3G 3C,5G 3U,5G 4G 3C,4G
     3C,4G
      ##STR742##
      0.05 3C 4C,8G 4C,9H 2C,9G 2C 0 0 1C 1C 2C 1C,2G 1H 1C,2G 1C,5H
      ##STR743##
      0.05 6Y,7C,9G 6C,9G 10C 6C,9G 1C,4G 2C,8G 2C 3C,7H 2C 2C,9G 2C,8H 2C,8G
     2C,9G 2C,9H
      ##STR744##
      0.05 2B 0 1C,3G 1C 1C 0 0 0 0 0 0 1H 5G 2C,8H
      ##STR745##
      0.05 1B 3G 0 0 0 0 0 0 0 0 0 0 0 0
      ##STR746##
      0.05 6Y,1B,2H 4C,9G 3C,9G 3C,9H 2C 2C,5G 1C 2C,6H 0 0 2C,8H 2C,9G 1C,3G
     1C,9G
      ##STR747##
      0.05 0 0 0 0 0 0 0 0 0 0 0 0 0 0
      ##STR748##
      0.05 3D,6Y 0 0 0 0 2G 0 2G 0 0 2C,7H 1H 8G 2C,9G
      ##STR749##
      0.4 9C 10C 10C 10C 9C 7C,9G 9C 9C 9C 9C 7U,9C 9C 8C 9C
      ##STR750##
      0.4 9C 9C 10C 10C 9C 9C 9C 9C 9C 9C 10C 9C 8C 9C
      ##STR751##
      0.4 9C 9C 10C 9C 9C 6C,9G 9C 9C 8C 4C,8G 5U,10C 6C,9G 5C,9G 6C,9G
      ##STR752##
      0.4 9C 9C 10C 9C 9C 9C 8C 9C 2C,8G 1C,5G 8U,9C 5C,9G 9C 2C,9G
      ##STR753##
      0.1 9C 9C 10C 10C 2C 1C 1C 3C 0 0 3C 9C 5C 2C
      ##STR754##
      0.05 7C,9G,6Y 6C,9G 10C 5C,9G 1C 9G 5G 4C,9H 2G 1C,6G 5C,9G 6H 8G 6C,9G
      ##STR755##
      0.04 9C 9C 10C 9C 9C 9C 9C 9C 9C 9C 6U,9C 9C 6C,9G 9C
      ##STR756##
      0.4 9C 9C 10C 9C 6C,9G 9C 9C 9C 9C 8C 5U,9C 9C 6C,9G 9C
      ##STR757##
      0.1 9C 9C 9C 3C 1C 2C 1C 9C 2C 1C 5C 9C 9C 5C
      ##STR758##
      1.0 0 0 0 0 0 0 0 0 0 0 0 0 0 0
      ##STR759##
      2.0 6C,9G,6Y 6C,9G 6C,9G 3C,9G 2C,7G 6C,7G 9C 10C 9C 9C 7U,9C 6C,9G
     4C,9G 9C
      ##STR760##
      0.05 2G,4G,6Y 3C,3H,7G 9C 3C,9G 1C 2C,5G,5X 3G 3C,8H 2C 1C,2G 2C,8G
     2H,9G,5X 8G 2H,9G
      ##STR761##
      0.05 3C,7G,6Y 3C,4H,9G 3C,9G 2C,9G 1C 2C,7G 1C 3C,9H 1C 1C 9H 2C,8G
     8G,5T 9G,5I
      ##STR762##
      0.05 3C,8G,6Y 4C,3H,9G 9C 9C 1C 2C,7G 1C,5G 9C 1C 1C,2G 3H,9G 3H,9G,5X
     9C 5C,9G
      ##STR763##
      0.05 1C 2C 1C 0 0 0 0 0 0 0 0 0 0 0
      ##STR764##
      0.05 5C,9G,6Y 5C,9G 4C,8G 10C 1C,3H 2C,9G 1C 2C,9H 0 0 1C 2C,9G 2C,8G
     2C,9H
      ##STR765##
      0.05 5C,9G,6Y 5C,9G 6C,9G 5C,9G 2C,4G 2C,9G 7G 9C 1C,6G 1C,6G 1C,4G
     2C,2H,8G 5C,9G 4C,9G
      ##STR766##
      0.05 2C,9G,6Y 5C,9G 5C,9G 2H,9G 1C,5G 8G 2C,6G 2C,7H 0 0 1C,3G 0 6G
     2C,9H
      ##STR767##
      0.05 1C,4G 2C,2H,8G 1C,5G 2G 1C,2G 1C,8G 1C,5G 1C,6G 0 1G 1C,2G 1H 8G
     7H
      ##STR768##
      0.05 5C,9G,6Y 4C,7G 2C,7G 2C,9G 1C 4C,9G 9G 5C,9H 0 2C,9G 2C,9H 0 9G
     1C,9G
      ##STR769##
      20.05 1C,1H0 00 00 00 00 00 4G0 6H0 00 00 00 1C0 00 2G0
      ##STR770##
      0.05 3C,5G,6Y 5C,9G 10C 5C,9G 2C,6G 9C 3C 2C,9H 0 2C 2C,7H 1C,5H 2C,8G
     9H
      ##STR771##
      0.1 0 0 0 0 0 0 0 0 0 0 0 0 0 0
      ##STR772##
      0.05 2H 2C,7G 1C 5G 1C 2C,8G 0 3C,9H 0 0 2G 0 5G 9G
      ##STR773##
      2.0 2C 2C 0 0 0 0 0 0 0 0 0 0 0 0
      ##STR774##
      0.4 5S,7G,6Y 5C,9G 3C,8G 5C,9G 0 5G 2C,6G 5C,9H 0 0 2C,6H 0 1C,7G 1C,5H
      ##STR775##
      0.1 0 2G,2C,3H 5G,2C 8G 0 0 0 0 0 0 0 0 0 0
      ##STR776##
      0.1 10G,8C 10G,7C 10G,3C 10G 7G 0 0 3G 0 0 3G 10G,4C 10G,3C 9G
      ##STR777##
      0.1 10G,8C 10G,8C 10C 10C 9G 7G 0 5G 2G 2G 4G 10G,4H 1C,9G 7G
      ##STR778##
      0.05 10G,3H,2C 9G,4H,3C 10G,3C 10G,3H,2C 3G 9G,1C 4G 9G,5H 4G 6G
     9G,2U,2C 9G 10G,2C 10G
      ##STR779##
      0.05 9C 10C 9C 10C 1C 9C 9G 6C 1C 1C 3U 6C 5C 10C
      ##STR780##
      0.05 9C 9C 3C,9G 9C 1C,3G 9C 5C,9G 9C 3G 3C,9G 4U,9C 3C,9H 5C,9G 5U,9G
      ##STR781##
      0.05 3C,9G,6Y 5C,9G 2C,9G 9C 1C,3G 3G 2G 2C,9H 0 0 1U,9G 3H,8H 2C,9G
     1U,9G
      ##STR782##
      0.05 9C 10C 9C 10C 2C 1C 2G 2C 0 0 2C 3C 2C 2C
      ##STR783##
      0.4 0 5C,8G 4C,9G 2H,7G 2C 0 2G 1H 0 0 2G 1G 3G 2G
      ##STR784##
      0.05 5G,6Y 3C,5H,9G 2C,8G 6G 1C,4G 3G 2G 2C,6H 0 0 5H 0 3C,9G 2C,9G
      ##STR785##
      0.05 3C,9G,6Y 6C,9G 2C,9G 10C 1C,3G 2C,8G 4G 2C,9H 1C 1C 2C,8H 2C,6H 7G
     2C,9G
      ##STR786##
      0.05 5C,9G,6Y 5C,9G 9C 2C,9G 1C,3G 2G 2G 5H 0 0 2G 2H,6G 6G 1H,7G
      ##STR787##
      0.05 5C,9G,6Y 6C,9G 6C,9G 6C,9G 1C,3G 2G 0 1H 0 0 2G 7H 5G 5G
      ##STR788##
      0.05 3C,8G,6Y 5C,9G 3C,9G 7G 1C 0 0 7H 0 0 0 0 0 6H
      ##STR789##
      0.05 3C,6Y -- 2C,9G 1C 1C 9G 6G 9H 0 2G 2C,8H 1C,2G 7G 9G
      ##STR790##
      0.05 2G,6F -- 0 0 0 0 0 0 0 0 0 0 0 0
      ##STR791##
      0.05 2C,5G,6Y 2C,3H,8G 2C 1C 1C,3G 5G 6G 3C,9H 0 0 1C 1C,3G 1C,7G 5C,9H
      ##STR792##
      0.05 0 -- 0 0 0 0 0 0 0 0 0 0 0 0
      ##STR793##
      0.05 2C,7G,6Y 5C,8G 4C,8G 3G 2C 5G 6G 5C,9H 4G 3G 3G 2C,2H 4C,9G 3C,9H
      ##STR794##
      0.05 0 -- 2C 0 1C 0 2H 1C 0 0 0 1H 0 1C
      ##STR795##
      0.05 3C,7G,6Y -- 2C,7G 2C,7H 1C 2C,7G 3C,8H 2C,9H 0 9G 2C,9H 2C 3C,9G
     1C,9G
      ##STR796##
      0.1 1C,6Y 0 1C 2G 0 0 0 3H 0 0 0 0 0 2C,7G
      ##STR797##
      0.4 6C,9G,6Y 6C,9G 10C 10C 2C,5G 8G 9C 9C 4C,9G 4C,9G 5U,9G 2C,2H,8G
     6C,9G 5U,9G
      ##STR798##
      0.05 2C,8G,6Y 3C,7G 2C,7G 2C,8G 1C 2G 0 0 0 0 3H 0 2C 2C,9H
      ##STR799##
      0.05 9C 9C 9C 9C 2C 9C 9C 10C 5C 9C 8U 10C 6C 5C
      ##STR800##
      0.05 9C 6C,9G 6C,9G 9C 3C,9G 5C,8G 5C,8G 10C 5C,9G 9C 7U,10C 6C,9G
     5C,9G 10C
      ##STR801##
      0.05 9C 5C,9G 9C 9C 2C,3H 2C,7G 6G 6C,9H 0 0 7U,9H 9C 2C,7G 2C,9G
      ##STR802##
      2.0 4S,7G,6Y -- 0 0 0 0 0 0 0 0 0 00 0
      ##STR803##
      2.0 5S,9G,6Y -- 1C 0 0 0 2C 2C,5H 0 0 1C,4H 3G 2H
      ##STR804##
      2.0 5S,8G,6Y -- 2C,5G 2C,8H 2C 0 3G 1H 0 2H 2C,8G 4G 2G
       PRE-EMERGENCE
      ##STR805##
      0.1 9G 9G 6G 10E 1C,7G 1C,9H 1C,6G 1C,9G 1C,9H 0 10E 10H
      ##STR806##
      0.1 9G 9H 8G 10E 1C,7G 1C,9H 1C,8G 1C,9G 9G 6H 10E 10E
      ##STR807##
      0.1 9G 9H 8G 10E 1C,8G 1C,9H 1C,8G 1C,9H 9G 6H 10E 1C,9H
      ##STR808##
      0.1 9G 8H 2C 0 0 1C,5G 0 0 1C,4G 0 10E 1C,9H
      ##STR809##
      0.4 5G 9G 2G 10E 3C 3C 0 0 1C,5H 1C,1H 10E 3C,9H
      ##STR810##
      0.1 9H 9H 6G 7G 5G 2C,7G 0 0 5G 2C,5H 10E 1C,7H
      ##STR811##
      0.1 9G 8H 8G 3G 2C 2C,8G 0 3G 1C,8G 2C,4G 9H 1C,9H
      ##STR812##
      0.4 5G,3C 6C,5G 4G 10E 4C,7G 5C,8G 3C,4G 10E  1C,3G 10E 7C,8G
      ##STR813##
      0.05 0 0 0 0 0 0 0 0 0 0 0 0
      ##STR814##
      0.05 9H 9H 5G 10E 1C 9H,3C 2C,7G 9G 1C,9H 1C,3H 4C,9H 2C,8H
      ##STR815##
      0.05 0 9H 2C 0 0 1C  0 1C,5G 0 2C 6H
      ##STR816##
      0.05 0 9H 0 0 0 0 0 0 0 0 0 0
      ##STR817##
      0.05 9G 5G 0 0 0 5H 0 0 1C,5C 2C,4H 1C,6G 2C
      ##STR818##
      0.05 0 0 0 0 0 0 0 0 0 0 0 0
      ##STR819##
      0.05 0 3C,8H 1H 0 0 1H 0 0 2G 3H 5G 6H
      ##STR820##
      0.4 9H 9H 10C 10E 10E 9H 5C,9H 10E 10E 9H 10E 10E
      ##STR821##
      0.4 9H 9H 9H 10E 10E 5C,9H 5C,9H 10E 10E 9H 10E 10E
      ##STR822##
      0.4 9G 9H 9G 9G 6C,9G 5C,9H 3C,9G 3C,9G 10E 9H 10E 6C,9H
      ##STR823##
      0.4 9H 9H 3C,9G 10E 3C,9H 5C,9H 3C,9G 1C,8H 3C,9H 9H 10E 6C,9H
      ##STR824##
      0.1 9G 9H 6G 10E 2G 3C,9H 2C,7G 1C,3G 3C,9G 9H 9H 4C,9G
      ##STR825##
      0.05 9G 9H 8G 10E 1C 2C,9H 1C,8G 1C,9G 1C,9G 1C,3G 10E 3C,9G
      ##STR826##
      0.04 9G 9H 6C,9G 10E 10E 3C,9H 2C,9H 10E 10E 9H 10E 2C,9G
      ##STR827##
      0.4 9G 9H 9G 9G 5C,9G 5C,9H 5C,9H 1C,9G 10E 9H 10E 10E
      ##STR828##
      0.1 9H 9H 9G 9G 2C,7G 5C,9H 3C,9G 9G 5C,9G 9H 10E 5C,9H
      ##STR829##
      1.0 0 0 0 0 0 0 0 0 0 0 0 0
      ##STR830##
      2.0 9C 9H 9G 10E 2C,9G 2C,9H 2C,9H 4C,9H 9H 9H 10E 5C,9H
      ##STR831##
      0.05 9G 9H 2G 2C,8G 1C 3C,8H 2C,5G 5G 1C,8G 2C,3G 8H 2C,3G
      ##STR832##
      0.05 8G 9H 4G 1C,8G 1C 9H,2C 2C,7G 2C,9G 2C,9H 8H 9H 1C,9G
      ##STR833##
      0.05 3G,9C 9H 5G 9G 2C,8G 9H 2C,8G 9H,2C 1C,9H 2C,6H 10E 7C,9H
      ##STR834##
      0.05 0 0 0 0 0 0 0 0 0 0 0 0
      ##STR835##
      0.05 8G 9H 0 9G 2C 2C,8H 1C,5G 1C,5G 2C,7G 1C 9H 2C,9H
      ##STR836##
      0.05 2C,9G 9H 6G,2C 2C,9G 3C,7G 5C,9H 2C,9G 1C,9G 2C,8G 2C,6H 10E 9C,9H
      ##STR837##
      0.05 9G 9H 0 9G 1C 2C,3G 1C 4G 2C,7G 0 2C,8H 2C,9G
      ##STR838##
      0.05 1H 8H 1H 9G 1C 3C,4G 3G 5G 6G 1H 8H 1C,7G
      ##STR839##
      0.05 5G 8H 0 10E 7G 2C,8G 2G 9G 2C,9H 0 1oE 2C,9H
      ##STR840##
      20.05 6H0 6H0 00 00 2G0 00 00 00 00 00 1C0 2G0
      ##STR841##
      0.05 9H 9H 1C 8G 3C 3C,9H 2C 1C,4G 3C,7G 2G 2C,9H 2C,9H
      ##STR842##
      0.1 0 0 0 0 0 0 0 0 0 0 0 0
      ##STR843##
      0.05 2G 9H 0 8G 0 7H 0 3G 2C,6G 0 3C,9H 9H
      ##STR844##
      2.0 6G 8H 0 0 0 4C 0 0 2C 0 0 2G
      ##STR845##
      0.4 8G 9H 2C 0 0 1C 0 0 2C 1C 5H 2C
      ##STR846##


0.1 5G 5G 0 0 0 0 0 0 0 0 4G 2G ##STR847## 0.1 9G 10E 8G 6G 3G 5G 0 4G 4G 9G 7G 6G ##STR848## 0.1 9G 6G 8G 5G 1G 3G 2G 2G 2G 9G 7G 6G ##STR849## 0.05 9G 7G 7G 9G 3G 3H,9G 6G 7G 9G 1G,2C 7G 9G ##STR850## 0.05 3C,9G 9HZ 6G 10E 5G 2C,9H 2C,9G 2C,9G 1U,9H 9H 10E 10H ##STR851## 0.05 9H -- 5G 10E 8G 2C,9H 2C,5G 9H 10E 1C,7H 10E 4C,9H ##STR852## 0.05 8H 9H 4G 0 0 2C,6H 0 3G 1C,9G 1C,5H 10E 2C,9H ##STR853## 0.05 10C -- 2C,9G 2C 1C 3C,9H 1C,4G 1C,4G 9G 2C,9H 10E 2C,9H ##STR854## 50 5G 9H 0 4G 0 0 0 0 4G 0 2C,8G 3H ##STR855## 0.05 7G 9G 3G 9G 0 2C 0 3G 1C,6G 0 2C,6G 2C ##STR856## 0.05 8G 9H 4C,3G 10E 2C 3C,7H 1C,4G 1C,5G 2C,8H 2H 3C,7G 2C,9H ##STR857## 0.05 9G 2C,9H 6G 2G 1C 0 0 0 1C,3G 1C,3G 1C 2C ##STR858## 0.05 9G 9H 2C,6G 1C,7G 1C,4G 1C,3H 2C 0 2C,5G 2C,5H 2C,4G 1C,3G ##STR859## 0.05 5G 3H 0 0 0 5H,2C 0 0 2G 0 2C,4G 2C,5G ##STR860## 0.05 8H 9H 2C 10E 3G 2C,6G 2G 8G 8H 0 9H 3C,9H ##STR861## 0.05 0 0 1C 0 2G 1C 0 0 2G 2G 5G 1C ##STR862## 0.05 5C,3C 7H 2C 8G 1C,3G 2C,4G 1C 3G 1C,4G 2G 5C,9H 4C,8G ##STR863## 0.05 1C 2G 0 0 0 0 0 0 0 0 0 0 ##STR864## 0.05 10E 10E 1C 5G 5G 5G 3G 4G 1C,4G 3G 3C,9H 3C,9H ##STR865## 0.05 0 2G 0 0 0 2H 2G 2G 1C,2G 0 2G 1C,5G ##STR866## 0.05 8G 9H 0 4G 1C 3C,9H 3G 2C,7G 9G 0 10E 1C,9G ##STR867## 0.1 0 0 0 0 0 0 0 0 0 0 0 0 ##STR868## 0.4 9H -- 7G 2C,7G 5C,9G 6C,9H 3C,9G 2C,9G 2C,9H 1C,2H 10E 5C,9H ##STR869## 0.05 0 8H 0 0 0 0 0 0 2C,5G 0 7H 2C,8H ##STR870## 0.05 9C 9H 9G 10E 5C,9G 5C,9H 2C,8G 10E 10E 3C,9H 10E 10E ##STR871## 0.05 9C 9H 9G 10E 5C,9G 2C,9H 2C,9G 10E 10E 9H 10E 10E ##STR872## 0.05 9C 9H 3C,9G 8G 5G 5C,9H 2C,4G 1C,6G 2C,9H 9H 10E 5C,9H ##STR873## 2.0 0 0 0 0 0 0 0 0 0 0 0 0 ##STR874## 2.0 5G -- 1C 0 3G 0 0 0 0 0 0 0 ##STR875## 2.0 5G 8H 3H 0 1C 2C 0 0 2G 0 2C,5H 1C,3G

TABLE B ______________________________________ PRE-EMERGENCE ON FALLSINGTON SILT LOAM ______________________________________ ##STR876## Rate kg/ha 0.03 0.12 ______________________________________ Crabgrass 8G,7C 10E Barnyardgrass 7G,3H 8G,9C Sorghum 10E 10E Wild Oats 2G 5G Johnsongrass 7G,3H 8G,5H Dallisgrass 3G 4G Giant foxtail 8G,8C 9G,9C Ky. bluegrass -- -- Cheatgrass 8G 7G Sugarbeets 8G,6C 8G,7C Corn 5G,5H 7G,5H Mustard 8G,8C 9G,9C Cocklebur 6G,3H 6G,3H Pigweed 10C 10C Nutsedge 7G 8G Cotton 8G 8G Morningglory 7G 8G Cassia 3G 3G Teaweed 5G 6G Velvetleaf 6G,3H 7G,5C Jimsonweed 6G,6C 6G,6C Soybean 0 4G Rice 10E 10E Wheat 3G,3C 4G,3C ______________________________________ ##STR877## Rate kg/ha 0.03 0.12 ______________________________________ Crabgrass 7G,5C 10C Barnyardgrass 7G,6C 8G,9C Sorghum 10E 10E Wild Oats 5G 7G Johnsongrass 6G,5H 9G,8C Dallisgrass 7G 8G Giant foxtail 6G,3C 9G,3C Ky. bluegrass -- -- Cheatgrass 8G 10E Sugarbeets 8G,7C 8G,7C Corn 5G,5H 4G,3H Mustard 9G,9C 9G,9C Cocklebur 7G,4C 6G,5H Pigweed 9G,9C 10C Nutsedge 7G 9G Cotton 8G 8G Morningglory 7G 8G Cassia 3G 4G Teaweed 4G 5G,2C Velvetleaf 7C,7C 10C Jimsonweed 5G 5G,3C Soybean 0 6G,4C Rice 10E 10E Wheat 7G,4C 7G,4C ______________________________________ ##STR878## Rate kg/ha 0.03 0.12 ______________________________________ Crabgrass 3G 4G Barnyardgrass 3G 5G Sorghum 3G 5G,3H Wild Oats 0 0 Johnsongrass 0 4G,3H Dallisgrass 3G 4G Giant foxtail 0 3G Ky. bluegrass 0 5G Cheatgrass 3G 5G Sugarbeets 0 3G Corn 2C 2C,2U Mustard 5G 7G Cocklebur 0 0 Pigweed 3G 4G Nutsedge 0 0 Cotton 0 3G Morningglory 3G 5G Cassia 0 0 Teaweed 0 0 Velvetleaf 0 0 Jimsonweed 0 0 Soybean 0 0 Rice 5G,5C 7G,8C Wheat 0 3G ______________________________________ ##STR879## Rate kg/ha 0.03 0.12 0.007 ______________________________________ Crabgrass 8G 9G,8C 6G Barnyardgrass 9G,7C 9G,7C 9G,7C Sorghum 10E 10E 8G,9C Wild Oats 6G,3H 8G,8C 6G,3H Johnsongrass 8G,3C 9G,9C 8G,5C Dallisgrass -- -- 5G Giant foxtail 6G,3H 9G,8C 3G Ky. bluegrass 7G,7C 8G,9C 7G Cheatgrass 10E 10E 10E Sugarbeets 9G,9C 9G,9C 7G,6C Corn 7G,5H 9G,9C 5G,2C Mustard 9G,9C 9G,9C 8G,8C Cocklebur 6G,3H 7G,5H 6G Pigweed 9G,8C 10E 10C Nutsedge 7G 6G 6G Cotton 7G 8G,3C 2G Morningglory 8G,3C 9G,8C 7G Cassia 7G 7G 5G Teaweed 6G 7G 2G Velvetleaf 8G,3C 10C 9G,5H Jimsonweed 7G 8G,4C 4G Soybean 4G 7G,5H 2G Rice 10E 10E 9G,9C Wheat 6G,3H 8G,8C 6G ______________________________________ ##STR880## Rate kg/ha 0.03 0.12 0.007 ______________________________________ Crabgrass 8G 9G,8C 7G Barnyardgrass 9G,8C 9G,9C 9C,8G Sorghum 10E 10E 9G,9C Wild Oats 7G,3H 8G,6C 4G Johnsongrass 8G,3C 10C 8G,3C Dallisgrass -- -- 5G Giant foxtail 9G,5H 10C 5G,2C Ky. bluegrass 9G,9C 10C 8G Cheatgrass 10E 10E 10E Sugarbeets 9G,9C 9G,9C 7G,8C Corn 7G,5H 9G,9C 7G,3H Mustard 9G,9C 10C 7G,8C Cocklebur 6G 8G,5H 4G Pigweed 10E 10E 9G,9C Nutsedge 5G 7G 5G Cotton 7G,3H 9G,8C 4G,2H Morningglory 8G,3C 9G,6C 7G,3C Cassia 7G 7G 4G Teaweed 7G 7G,5C 4G Velvetleaf 8G,6C 10C 8G,5H Jimsonweed 7G,5C 9G,9C 4G Soybean 7G,5H 8G,5H 3G Rice 10E 10E 9G,9C Wheat 6G 8G,8C 5G ______________________________________ ##STR881## Rate kg/ha 0.03 0.12 0.007 ______________________________________ Crabgrass 7G,3C 9G,9C 2G Barnyardgrass 6G,3C 7G,3C 4G Sorghum 8G,3C 10C 8G,3H Wild Oats 4G 6G 2G Johnsongrass 8G,4C 8G,4C 4G Dallisgrass 0 5G 0 Giant foxtail 0 7G,3H 0 Ky. bluegrass 8G,8C 8G,8C 0 Cheatgrass 5G 7G,3H 3G Sugarbeets 9G,9C 10C 10C Corn 9G,7C 9G,9C 7G,3H Mustard 10C 10C 10C Cocklebur 8G,5H 9G,5H 6G Pigweed 9G,9C 10C 9G,9C Nutsedge 6G 6G 3G Cotton 8G,5H 8G,5H 6G,3H Morningglory 8G,3H 9G,5H 9G,8C Cassia 9G,8C -- 7G Teaweed 7G,3C 7G,3C 4G Velvetleaf 9G,9C 10C 8G Jimsonweed 6G,5C 7G,7C 5G Soybean 9G,5H 9G,5H 6G,3H Rice 10E 10E 6G Wheat 4G 4G 0 ______________________________________ ##STR882## Rate kg/ha 0.03 0.12 0.007 ______________________________________ Crabgrass 3G 6G,3C 0 Barnyardgrass 5G 7G,4C 4G Sorghum 8G,3H 9G,9C 7G,3H Wild Oats 2G 4G 0 Johnsongrass 5G,3H 7G,3H 5G Dallisgrass 0 6G 2G Giant foxtail 0 3G 0 Ky. bluegrass 6G 8G,8C 3G Cheatgrass 0 7G 0 Sugarbeets 10C 9G,9C 9G,9C Corn 6G,3H 6G,5H 2G,1U Mustard 10C 10C 10E Cocklebur 6G 7G,5H 6G Pigweed 8G,8C 10C 7G,5E Nutsedge 2G 7G 6G Cotton 6G,5H 9G,5H 6G,3H Morningglory 8G,3H 8G,3H 9G,8C Cassia 6G -- 4G Teaweed 6G,2C 7G,3C 3G Velvetleaf 8G,5H 8G,8C 6G Jimsonweed 5G 6G,3C 5G Soybean 5G 9G,5H 4G,3H Rice 7G 10E 5G Wheat 2G 2G 0 ______________________________________ ##STR883## Rate kg/ha 0.03 0.12 ______________________________________ Crabgrass 0 0 Barnyardgrass 3G 3G Sorghum 0 6G,3H Wild Oats 0 0 Johnsongrass 0 5G,3H Dallisgrass 0 3G Giant foxtail 0 2H Ky. bluegrass 4G 6G Cheatgrass 0 10E Sugarbeets 3G 3G Corn 0 0 Mustard 8G,5C 10C Cocklebur 0 0 Pigweed 4G 8G,8C Nutsedge 0 7G Cotton G 3G Morningglory 3G 4G Cassia 0 0 Teaweed 0 3G Velvetleaf 5G,3H 6G,3H Jimsonweed 3G 5G Soybean 0 2G Rice 4G 5G,3H Wheat 0 0 ______________________________________ ##STR884## Rate kg/ha 0.03 0.12 ______________________________________ Crabgrass 0 0 Barnyardgrass 6G 6G,5H Sorghum 7G,3H 10C Wild Oats 3G 3G Johnsongrass 6G,3H 8G,5E Dallisgrass 0 4G Giant foxtail 0 3G Ky. bluegrass 7G,4C 7G,4C Cheatgrass 7G,5C 9G,9C Sugarbeets 6G,3H 10C Corn 4G,2U 6G,5H Mustard 10C 10C Cocklebur 2G 3G Pigweed 8G,8C 10C Nutsedge 7G 7G Cotton 5G 5G,2H Morningglory 5G 4G Cassia 5G 5G Teaweed 2G 4G Velvetleaf 8G,5H 9G,5H Jimsonweed 8G 8G Soybean 4G 4G Rice 7G 8G Wheat 4G 6G ______________________________________ ##STR885## Rate kg/ha 0.03 0.12 ______________________________________ Crabgrass 8G,5C 9G,7C Barnyardgrass 9G,7C 9G,7C Sorghum 10E 10E Wild Oats 7G,3C 8G,5E Johnsongrass 9G,7C 9G,9C Dallisgrass 7G 8G Giant foxtail 7G,3H 9G,5H Ky.

bluegrass 10C 9G,9C Cheatgrass 10C 10E Sugarbeets 9G,9C 9G,9C Corn 7G,5H 8G,3C Mustard 10C 10E Cocklebur 6G 7G Pigweed 10E 10E Nutsedge 8G 10E Cotton 3G 7G,5H Morningglory 6G 8G,3H Cassia 5G 7G Teaweed 6G 8G,4C Velvetleaf 8G,7C 10C Jimsonweed 6G 7G,7C Soybean 3G 6G,3H Rice 10E 10E Wheat 7G,3C 7G,5C ______________________________________ ##STR886## Rate kg/ha 0.03 0.12 0.007 ______________________________________ Crabgrass 7G,3H 8G,5C 0 Barnyardgrass 6G,3H 8G,4C 0 Sorghum 9G,9C 10E 5G,3H Wild Oats 2G 7G,3H 0 Johnsongrass 8G,5H 8G,5C 0 Dallisgrass 6G 0 0 Giant foxtail 5G,2H 7G,5H 0 Ky. bluegrass 7G,7C 7G,5C 0 Cheatgrass 7G,3C 10C 0 Sugarbeets 9G,9C 9G.9C 5G,3H Corn 10C 10E 3G Mustard 10C 10C 7G,3C Cocklebur 7G,5H 8G,5H 2G Pigweed 10C 10C 5G Nutsedge 6G 7G 0 Cotton 7G 8G,5H 0 Morningglory 8G,3H 8G,3H 6G,5H Cassia 6G -- 0 Teaweed 6G 7G,4C 0 Velvetleaf 8G,8C 8G,8C 3G Jimsonweed 6G,4C 6G,5C 0 Soybean 2H 7G,5H 0 Rice 10E 10E 7G,3H Wheat 5G 6G 0 ______________________________________ ##STR887## Rate kg/ha 0.03 0.12 ______________________________________ Crabgrass 0 5G Barnyardgrass 5G,3H 4G,2H Sorghum 8G,5H 10C Wild Oats 0 3C Johnsongrass 7G,3H 8G,5H Dallisgrass 0 4G Giant foxtail 0 4H Ky. bluegrass 7G 8G,8C Cheatgrass 10E 10E Sugarbeets 6G,3H 10C Corn 5G,3H 6G,5H Mustard 8G,5C 10C Cocklebur 0 5G Pigweed 5G 10E Nutsedge 0 5G Cotton 3G 6G,3H Morningglory 4G 5G Cassia 3G 3G Teaweed 3G 4G,2C Velvetleaf 3H 6G,3H Jimsonweed 3G 7G,3C Soybean 0 4G,3H Rice 6G 7G,5H Wheat 3G 3G ______________________________________ ##STR888## Rate kg/ha 0.12 0.5 ______________________________________ Crabgrass 0 0 Barnyardgrass 0 0 Sorghum 0 7G,5H Wild Oats 0 4G Johnsongrass 0 5G Dallisgrass 0 3G Giant foxtail 0 2G Ky. bluegrass -- -- Cheatgrass 0 5G Sugarbeets 2G 6G Corn 0 4G Mustard 8G,5C 10C Cocklebur 6G,3C 6G,2C Pigweed 4G,4C 7G,7C Nutsedge 0 5G Cotton 3G 7G Morningglory 0 6G Cassia 0 3G Teaweed 0 0 Velvetleaf 4G,3C 5G Jimsonweed 0 0 Soybean 0 4G,2H Rice 0 2G Wheat 0 3G ______________________________________ ##STR889## Rate kg/ha 0.06 0.12 0.5 ______________________________________ Crabgrass 6G,7C 4G 7G Barnyardgrass 4G 6G 8G,4C Sorghum 9G,5C 9G,8C 10C Wild Oats 0 0 0 Johnsongrass 4G,3H 4G 7G,3H Dallisgrass 0 0 3G Giant foxtail 3G 3G 6G,3C Ky. bluegrass 3G 3G 5G Cheatgrass 3G -- -- Sugarbeets 9G,9C 10C 10C Corn 5G 6G,3H 9G,5H Mustard 10C 8G 10C Cocklebur 6G,3H 7G,3H 8G,5H Pigweed 8G,8C 10C 10E Nutsedge 3G 7G 8G Cotton 8G,3H 9G,5C 9G,5C Morningglory 8G,3H 8G,3H 9G,9C Cassia 6G 5G 7G Teaweed 5G,3H 4G 8G,5C Velvetleaf 8G,7C 10C 10C Jimsonweed 9G,9C 7G 10C Soybean 0 3G 5G,3H Rice 10E 8G,6C 10E Wheat 0 0 0 ______________________________________


Wheat and Barley Herbicide Screen

Two ten-inch in diameter plastic pans lined with polyethylene liner were filled with prepared Fallsington silt loam soil. One pan was planted with seeds of wheat (Triticum aestivum), barley (Hordeum vulgare), wild oats (Avena fatua), downy brome (Bromus tectorum), cheatgrass (Bromus secalinus), blackgrass (Alopecurus myosuroides), annual bluegrass (Poa annua), green foxtail (Setaira viridis), quackgrass (Agropyron repens), Italian ryegrass (Lolium multiflorum) and ripgut brome (Bromus rigidus). The other pan was planted with seeds of Russion thistle (Salsola kali), tansy mustard (Descuraina pinnata), smartweed (Polygonum pennsylvanicum), tumble mustard (Sisymbrium altissium), kochia (Kochia scoparia), shepherd's purse (Capsella bursa-pastoris), Matricaria indora, black nightshade (Solanum nigrum), yellow rocket (Barbarea vulgaris), wild mustard (Brassica kaber) and wild buckwheat (Polygonum convolvulus). The above two pans were treated preemergence. At the same time two pans in which the above plant species were growing were treated postemergence. Plant height at the time of treatment ranged from 1-15 cm depending on plant species.

The compounds applied were diluted with a non-pytotoxic solvent and sprayed over-the-top of the pans. An untreated control and a solvent alone control were included for comparison. All treatments were maintained in the greenhouse for 20 days at which time the treatments were compared to the controls and the effects visually rated. The recorded data are presented in Table C. It will be seen that the compounds have utility for selective weed control in cereal crops.

                  TABLE C
    ______________________________________
           Post-emergence
                         Pre-emergence
    ______________________________________
            ##STR890##
    Rate kg/ha
             0.008           0.008
    wheat    1C,1G           0
    barley   1G              1G
    wild oats
             1C,1G           0
    downy brome
             2G              2G
    cheatgrass
             1C,4G           7G
    blackgrass
             3C,3G           5G
    annual   8C,8G           3C,6G
    bluegrass
    green foxtail
             1C,3G           1C,2G
    quackgrass
             2C,3G           3G
    Italian  6C,7G           1C,5G
    ryegrass
    ripgut brome
             1C,2G           0
    Russian  10C             3G
    thistle
    tansy mustard
             10C             10C
    smartweed
             --              --
    jimhill  10C             10C
    mustard
    Kochia   10C             10C
    shepherd's
             10C             10C
    purse
    false    10C             6C,7G
    chamomile
    black    10C             7G
    nightshade
    yellow rocket
             10C             10C
    wild mustard
             10C             10C
    wild     10C             7C,6G
    buckwheat
    Rate kg/ha
             0.03            0.03
    wheat    6C,5G           0
    barley   2C,3G           2G
    wild oats
             7C,5G           0
    downy brome
             7C,7G           5C,7G
    cheatgrass
             10C             10C
    blackgrass
             9C,8G           7C,7G
    annual   10C             7C,8G
    bluegrass
    green foxtail
             10C             5C,6G
    quackgrass
             10C             2C,5G
    Italian  10C             5C,7G
    ryegrass
    ripgut brome
             3C,4G           1C,3G
    Russian  10C             7C,6G
    thistle
    tansy mustard
             10C             10C
    smartweed
             --              --
    jimhill  10C             10C
    mustard
    Kochia   10C             10C
    shepherd's
             10C             10C
    purse
    false    10C             10C
    chamomile
    black    10C             7C,8G
    nightshade
    yellow rocket
             10C             10C
    wild mustard
             10C             10C
    wild     10C             7C,7G
    buckwheat
            ##STR891##
    Rate kg/ha
             0.015           0.015
    wheat    0               0
    barley   0               0
    wild oats
             0               2C,2G
    downy brome
             0               1C,3G
    cheatgrass
             0               1C,4G
    blackgrass
             0               3G
    annual   0               2G
    bluegrass
    green foxtail
             0               0
    quackgrass
             0               0
    Italian  0               0
    ryegrass
    ripgut brome
             0               0
    Russian  10C             0
    thistle
    tansy mustard
             10C             10C
    smartweed
             --              --
    jimhill  10C             10C
    mustard
    Kochia   10C             2C,5G
    shepherd's
             10C             10C
    purse
    false    10C             4C,6G
    chamomile
    black    0               2C,6G
    nightshade
    yellow rocket
             10C             3C,8G
    wild mustard
             10C             9C,9G
    wild     3C,2G           4G
    buckwheat
            ##STR892##
    Rate kg/ha
             0.06            0.06
    wheat    2G              0
    barley   0               0
    wild oats
             0               3C,4G
    downy brome
             0               4C,6G
    cheatgrass
             7C,5G           10C
    blackgrass
             7C,7G           10C
    annual   2G              3C,5G
    bluegrass
    green foxtail
             1C,3G           2C,4G
    quackgrass
             0               2C,3G
    Italian  0               0
    ryegrass
    ripgut brome
             0               0
    Russian  10C             7C,8G
    thistle
    tansy mustard
             10C             10C
    smartweed
             --              --
    jimhill  10C             10C
    mustard
    Kochia   10C             7C,7G
    shepherd's
             10C             10C
    purse
    false    10C             7C,9G
    chamomile
    black    0               2C,7G
    nightshade
    yellow rocket
             10C             9C,9G
    wild mustard
             10C             10C
    wild     7C,6G           2C,7G
    buckwheat
            ##STR893##
    Rate kg/ha
             0.015           0.015
    wheat    0               0
    barley   0               0
    wild oats
             0               0
    downy brome
             0               2G
    cheatgrass
             0               1G
    blackgrass
             0               3G
    annual   0               2G
    bluegrass
    green foxtail
             0               0
    quackgrass
             0               0
    Italian  0               0
    ryegrass
    ripgut brome
             0               0
    Russian  10C             2C,2G
    thistle
    tansy mustard
             10C             10C
    smartweed
             --              --
    jimhill  10C             10C
    mustard
    Kochia   2C,4G           3C,5G
    shepherd's
             10C             10C
    purse
    false    10C             7C,8G
    chamomile
    black    1C,3G           1C,8G
    nightshade
    yellow rocket
             2C,3G           5C,6G
    wild mustard
             10C             9C,9G
    wild     9C,8G           4C,7G
    buckwheat
    Rate kg/ha
             0.06            0.06
    wheat    0               0
    barley   0               0
    wild oats
             0               0
    downy brome
             2C,3G           2C,3G
    cheatgrass
             2C,5G           1C,5G
    blackgrass
             1C,3G           2C,7G
    annual   1C,4G           5G
    bluegrass
    green foxtail
             2G              2C,3G
    quackgrass
             0               1C,2G
    Italian  3G              3G
    ryegrass
    ripgut brome
             0               0
    Russian  10C             7C,8G
    thistle
    tansy mustard
             10C             10C
    smartweed
             --              --
    jimhill  10C             10C
    mustard
    Kochia   7C,7G           7C,7G
    shepherd's
             10C             10C


purse false 10C 9C,9G chamomile black 3C,6G 2C,8G nightshade yellow rocket 10C 6C,8G wild mustard 10C 9C,9G wild 10C 7C,7G buckwheat ##STR894## Rate kg/ha 0.008 0.008 wheat 0 0 barley 0 0 wild oats 0 0 downy brome 0 1C,2G cheatgrass 0 3G blackgrass 1G 1C,3G annual 1G 5C,6G bluegrass green foxtail 2G 0 quackgrass 0 2G Italian 0 4G ryegrass ripgut brome 0 0 Russian 10C 4C,5G thistle tansy mustard 10C 10C smartweed -- -- jimhill 10C 10C mustard Kochia 8C,8G 7C,8G shepherd's 9C,8G 10C purse false 10C 7C,8G chamomile black 1G 2C,5G nightshade yellow rocket 10C 10C wild mustard 10C 10C wild 8C,7G 4C,7G buckwheat Rate kg/ha 0.03 0.03 wheat 0 0 barley 0 0 wild oats 0 0 downy brome 1G 2C,5G cheatgrass 2G 2C,5G blackgrass 1C,3G 3C,7G annual 3G 5C,7G bluegrass green foxtail 2C,3G 3G quackgrass 1G 2C,7G Italian 2G 1G ryegrass ripgut brome 0 Russian 10C 10C thistle tansy mustard 10C 10C smartweed -- -- jimhill 10C 10C mustard Kochia 10C 8C,9G shepherd's 10C 10C purse false 10C 9C,9G chamomile black 2C,3G 3C,8G nightshade yellow rocket 10C 10C wild mustard 10C 10C wild 10C 8C,8G buckwheat ______________________________________