Heterocyclic azo dyes with couplers having sulfoaralkyl groups

Abstract

This invention relates to azo dyes prepared by diazotizing substituted or unsubstituted heterocyclic amines such as 2-aminothiophene and coupling with certain aniline, tetrahydroquinoline, or benzomorpholine compounds containing sulfoaralkyl groups. These dyes are particularly useful in dyeing polyamide fibers, cellulose acetate fibers and wool.

Description

This invention concerns novel dyes which comprise heterocyclic diazo moieties and aromatic amine couplers having sulfoaralkyl groups. These dyes are substantially water soluble and are particularly useful for dyeing polyamide, wool and the like and generally exhibit excellent properties including fastness to light and dyeability.

The dyes of this invention correspond to the following general formula: ##STR1## wherein R is a heterocyclic radical selected from benzothiazol-2-yl, 2,1-benzisothiazol-3-yl, 1,3,4-thiadiazol-2-yl, 1,2,4-thiadiazol-5-yl, isothiazol-5-yl, pyrazol-5-yl, thiophen-2-yl, and thiazol-2-yl, each of which radicals may be substituted as further defined below; each R.sub.1 and Z are selected independently from alkyl, alkoxy, alkenyl of 2-6 carbons, halogen, acylamido, and alkylthio; R.sub.2 is selected from hydrogen, alkyl, alkenyl of 2-6 carbons, aryl, cycloalkyl, and ##STR2## and R.sub.2 in conjunction with R.sub.1 may form a 1,2,3,4-tetrahydroquinoline or a 2,3-dihydro-1,4-benzoxazine (benzomorpholine) ring as defined in more detail below; M is H.sup.+, Na.sup.+, K.sup.+, or NH.sub.4 ; n is 1-6; and m is 0, 1 or 2.

More particularly the dyes correspond to the formula above wherein R is selected from ##STR3## wherein

Ring A may have 1-3 substituents selected from alkyl, alkoxy, thiocyano, alkylthio, cyano, carbamoyl, alkylcarbamoyl, alkoxycarbonyl, acyl, alkylsulfonyl, sulfamoyl, SO.sub.2 NH(alkyl), SO.sub.2 N(dialkyl), alkylsulfonamido, acylamido, halogen, trifluoromethyl, and SO.sub.3 (aryl);

Ring B may have 1-3 substituents selected from alkyl, alkoxy, chlorine, bromine, SO.sub.2 NH.sub.2, SO.sub.2 NH(alkyl), and SO.sub.2 N(dialkyl);

Ring C may have a substituent selected from alkyl, alkoxy, halogen, alkylsulfonyl, SO.sub.2 NH.sub.2, SO.sub.2 NH(alkyl), SO.sub.2 N(dialkyl), arylsulfonyl, acylamido, aryl, arylthio, alkenylthio, cyclohexylthio, thiocyano, cyclohexylsulfonyl, alkylthio, and cyclohexyl;

Ring D may have a substituent selected from alkyl, aryl, halogen, alkylthio, cyclohexylthio, and alkylsulfonyl;

Ring E may have 1 or 2 substituents selected from alkyl, halogen, cyano, carbamoyl, CONH alkyl, alkoxycarbonyl, alkylthio, alkenylthio, arylthio cyclohexylthio, S-heterocycle, aryloxy, and alkoxy;

Ring F may have 1 or 2 substituents selected from alkyl, alkoxycarbonyl, alkylthio, aryl, cyano, carbamoyl, alkylcarbamoyl, and alkylsulfonyl, and the hydrogen on the 1-position nitrogen may be replaced with alkyl, aryl of 6-10 carbons, alkylsulfonyl, arylsulfonyl, alkanoyl, or alkoxycarbonyl;

Ring G may be substituted with 1-3 groups selected from alkyl, cyano, alkoxycarbonyl, acyl, alkylsulfonyl, arylsulfonyl, carbamoyl, alkylcarbamoyl, aryl, aroyl, halogen, sulfamoyl, hydroxyalkylcarbamoyl, alkylsulfamoyl, and formyl;

Ring H may have one or two substituents selected from alkyl, aryl, alkoxycarbonyl, carbonyl, CONH(alkyl), CON(alkyl).sub.2, halogen, cyano, thiocyano, alkylthio, alkylsulfonyl, arylsulfonyl, formyl, acyl, and aroyl;

and substituent A is selected from H, phenyl, phenylsulfonyl, alkanoyl, alkoxycarbonyl, alkyl, halophenyl, alkylphenyl, alkylsulfonyl, hydroxyalkyl, alkylphenylsulfonyl and cyclohexylsulfonyl.

The couplers are described more particularly by the following formulae: ##STR4## wherein R.sub.1, Z, M, m and n are as defined above, and R.sub.3 and R.sub.4 are each selected from hydrogen and alkyl.

All of the above defined alkyl, alkoxy, alkylene, alkenyl and cyclic moieties in the definitions of R.sub.1, R.sub.2 and Z, and the thiophene ring substituents may bear up to three substituents selected from hydroxy, alkoxy, aryl, aryloxy, cyclohexyl, furyl, alkylcyclohexyl, aroyloxy, alkoxycarbonyl, alkanoyloxy, sulfamoyl, SO.sub.2 NH(aryl), SO.sub.2 NH(alkyl), SO.sub.2 N(dialkyl), NHCOO(alkyl), NHCONH(alkyl), acylamido, alkylsulfonamido, succinimido, glutarimido, phthalimido, 2-pyrrolidono, cyano, carbamoyl, alkylcarbamoyl, alkoxyalkoxy, alkylthio, halogen, arylthio, alkylsulfonyl and arylsulfonyl.

The various alkyl, alkylene, alkoxy, alkanoyl and the like moieties within the above definitions of R, R.sub.1, R.sub.2 and Z are of 1-6 carbons, and they and the alkenyl groups may be straight or branched chain.

The dyes of this invention impart red to blue shades on fibers, particularly polyamides, and are especially useful for dyeing polyamide (nylon) carpets, exhibiting improvements in one or more properties such as fastness to light, ozone, oxides of nitrogen, pesticides, insecticides such as organophosphorous compounds (e.g. Malathion.RTM.), washing, sublimation and crocking and leveling, transfer, exhaustion and build.

The heterocyclic amines used in this invention are prepared according to procedures well known to the art. The couplers may be sulfonated prior to or after coupling, and the dye may be isolated when M is H.sup.+, but usually is isolated as the sodium or potassium salt. The following examples wherein moles are designated "m" will further illustrate the preparations.

EXAMPLE 1

Preparation of .alpha.-(N-Ethylanilino)-Toluenesulfonic Acid

To 30.0 g. of 100% sulfuric acid is added N-benzyl-N-ethylaniline (30.0 g) dropwise below about 50.degree. C. To this solution is added, at 50.degree.-60.degree. C., 60% oleum (30.0 g.) with good stirring. The mixture is stirred and heated at about 60.degree. C. for three hours and then drowned into 200 ml of water. The free sulfonic acid which is mostly the meta isomer with a small amount of para, precipitates on standing and is collected by filtration, washed with water, and dried. N-Benzylanilines containing groups such as alkyl, alkoxy, and halogen in the ortho, meta, or para positions of the benzyl group may be sulfonated by this procedure. The exact location of the sulfonic acid group in these cases is often not known and mixtures usually are produced.

Aromatic amines which contain N-aralkyl groups and which can be sulfonated by the above procedure include:

______________________________________EXAMPLE NO.______________________________________2 N--Benzyl-N--ethyl-m-toluidine3 N--Benzyl-2,7-dimethyl-1,2,3,4- tetrahydroquinoline4 N--Benzyl-2,3-dihydro-3,6-dimethyl- 1,4-benzoxazine5 N--Methyl-N--(2-phenylethyl)aniline6 N--Ethyl-N--(4-phenylbutyl)-3- chloroaniline7 N,N--Dibenzylaniline8 N--Benzyl-2,5-dimethylaniline9 N--Benzyl-2-methoxy-5-methylaniline10 N--Benzyl-2-methoxy-5-chloroaniline11 N--Benzyl-N--cyclohexylaniline______________________________________

EXAMPLES 12-21

Diazotization and Coupling of 2-Amino-6-methylbenzothiazole

To 150 g. of 60% acetic acid containing 10 g. of concentrated H.sub.2 SO.sub.4 is added 8.2 g. (0.05 m) of 2-amino-6-methylbenzothiazole at room temperature. The solution is cooled to -5.degree. C., and a solution of 3.6 g. NaNO.sub.2 in 20 ml of concentrated H.sub.2 SO.sub.4 is added below 0.degree. C. The reaction mixture is stirred at -5.degree. to 0.degree. C. for 1.5 hours. Each of the couplers (0.005 m) listed below as Examples 1-10 is added to water, or a 0.005 mole aliquot of the coupler in dilute sulfuric acid is added to water, and cooled in an ice bath.

To each chilled coupler is added a 0.005 mole aliquot of the diazonium solution. The coupling mixture is treated with enough potassium acetate to neutralize the mineral acid. Water is added to the coupling mixture to a total volume of about 200 ml and the dyes collected by filtration, washed with 10% KCl solution, and dried in air. The dyes usually are admixed with about an equal weight of K.sub.2 SO.sub.4 and are used for dyeing without further purification to produce red shades on polyamides.

EXAMPLES 22-31

Diazotization and Coupling of 3-Amino-2,1-benzisothiazole

To 25 ml of concentrated H.sub.2 SO.sub.4 is added 3.6 g. of NaNO.sub.2 portionwise below 80.degree. C. The solution is cooled and 50 ml of 1:5 acid (1 part propionic, 5 parts acetic acid) is added below 20.degree. C. The mixture is further cooled and 3-amino-2,1-benzisothiazole (7.5 g., 0.05 m) is added, followed by 50 ml of 1:5 acid, all at 0.degree.-5.degree. C. The diazonium, after stirring at 0.degree.-5.degree. C. for 1 hr., is coupled to each of the couplers of Examples 1-10 in a similar manner as above to produce violet to reddish blue dyes for polyamides.

EXAMPLES 32-41

Diazotization and Coupling of 2-Amino-5-ethylthio-1,3,4-thiadiazole

Sodium nitrite (3.6 g.) is added portionwise to 25 ml of concentrated H.sub.2 SO.sub.4. The solution is cooled and 100 ml of 1:5 acid is added below 15.degree. C. The mixture is cooled and 8.05 g. (0.05 m) of 2-amino-5-ethylthio-1,3,4-thiadiazole is added below 10.degree. C. After stirring at 0.degree.-5.degree. C. for two hrs., a 0.005 m aliquot of the diazonium salt is coupled to 0.005 m of each of the couplers of Examples 1-10 to produce red dyes for polyamides.

EXAMPLES 42-51

Diazotization of 5-Amino-3-ethylthio-1,2,4-thiadiazole

5-Amino-3-ethylthio-1,2,4-thiadiazole (8.05 g., 0.05 m) is diazotized exactly as described in Examples 28-37 and a 0.005 m aliquot coupled to a 0.005 m portion of each of the couplers of Examples 1-10 in the manner previously illustrated.

EXAMPLES 52-61

Diazotization of 5-Amino-3-methyl-4-cyanoisothiazole

To 25 ml of concentrated H.sub.2 SO.sub.4 is added 3.6 g. of NaNO.sub.2 allowing the temperature to rise. The solution is cooled and 50 ml of 1:5 acid is added below 10.degree. C. Stirring is continued and 6.95 g. (0.05 m) of 5-amino-3-methyl-4-cyanoisothiazole is added below 5.degree. C., followed by an additional 50 ml of 1:5 acid. After stirring at 0.degree.-5.degree. C. for two hrs., a 0.005 m aliquot of the diazonium salt is coupled to 0.005 m of each of the couplers of Examples 1-10 as previously described to produce rubine to violet dyes for polyamides.

EXAMPLES 62-71

Diazotization of 5-Amino-4-carbomethoxypyrazole

Nitrosyl sulfuric acid is prepared by adding 3.6 g. NaNO.sub.2 to 25 ml of concentrated H.sub.2 SO.sub.4. The solution is cooled and 100 ml of 1:5 acid is added below 20.degree. C. After further cooling, 5-amino-4-carbomethoxypyrazole (7.05 g., 0.05 m) is added at 0.degree.-5.degree. C. and stirring continued for two hrs. A 0.005 m aliquot of the diazonium solution is coupled to 0.005 m of each of the couplers of Examples 1-10 in the manner previously described to produce red dyes for polyamides.

EXAMPLES 72-81

Diazotization of 2-Amino-3-carbomethoxy-5-isobutyrylthiophene

To 150 g. of 60% aqueous acetic acid is added 11.35 g. (0.05 m) of 2-amino-3-carbomethoxy-5-isobutyrylthiophene at room temperature. Ten grams of concentrated H.sub.2 SO.sub.4 is added and the mixture cooled to 0.degree. C. A solution of 3.6 g NaNO.sub.2 in 25 ml of conc. H.sub.2 SO.sub.4 is added below 10.degree. C. and stirring continued for 1 hr. at 0.degree.-5.degree. C. A 0.005 m aliquot of this diazonium salt is coupled to a 0.005 m portion of each of the couplers of Examples 1-10 as previously illustrated to produce violet to reddish-blue dyes for polyamides.

EXAMPLES 82-91

Diazotization of 2-amine-5-carbethoxy-4-methylthiazole

Sodium nitrite (3.6 g.) is added portionwise to 25 ml of concentrated H.sub.2 SO.sub.4. The solution is cooled and 100 ml of 1:5 acid is added below 15.degree. C. The mixture is cooled and 9.31 g (0.05 m) of 2-amino-5-carbethoxy-4-methylthiazole is added below 10.degree. C. After stirring at 0.degree.-5.degree. C. for two hrs., a 0.005 m aliquot of the diazonium salt is coupled to 0.005 m of each of the couplers of Examples 1-10 to produce red to violet dyes for polyamide fibers.

METHOD II

EXAMPLE 92

Preparation of Intermediate Dye

Sodium nitrite (0.72 g) is added portionwise to 5 ml of concentrated H.sub.2 SO.sub.4. The solution is cooled and 20 ml of 1:5 acid is added below 15.degree. C. The mixture is cooled and 1.61 g. (0.01 m) of 2-amino-5-ethylthio-1,3,4-thiadiazole is added below 10.degree. C. After stirring at 0.degree.-5.degree. C. for two hrs., the diazonium solution is added to a chilled solution of N-benzyl-N-ethylaniline (0.01 m) dissolved in 40 ml. of 1:5 acid. The solution is kept cold and ammonium acetate added until neutral to Congo Red test paper. After allowing to stand for 1 hr., the coupling mixture is diluted with water, and the dye is filtered, washed, and dried in air.

EXAMPLE 93

Sulfonation of Dye Containing N-(Aralkylamino) Group

A portion of the dye from Example 92 (1.5 g) is added portionwise to 15 ml. of concentrated H.sub.2 SO.sub.4 over 20 min., allowing the temperature to rise to 30.degree. C. The reaction mixture is then heated at 70.degree. C., when the reaction is completed as evidenced by thin-layer chromatography. After the reaction mixture is drowned on ice-water mixture, 50% NaOH is added until the pH is about 7. The dye is collected by filtration, washed with water, and dried in air. The structure is as follows: ##STR5## The dye produces bright orange shades on polyamide and has good fastness properties.

TABLE I__________________________________________________________________________ ##STR6##Substituents onRing A (R.sub.1).sub.m R.sub.2 Z n M__________________________________________________________________________None None C.sub.2 H.sub.5 H 1 K.sup.+" " C.sub.6 H.sub.11 " " "" " C.sub.6 H.sub.5 " " "" 3CH.sub.3 C.sub.2 H.sub.5 " " "" " CH.sub.2 C.sub.6 H.sub.5 " " "" " CH.sub.2 CH.sub.2 OCH.sub.3 " " "" " CH.sub.2 CH.sub.2 CONH.sub.2 " " "" " CH.sub.2 CH.sub.2 Cl " " "" 3-NHCOCH.sub.3 C.sub.2 H.sub.5 " " "" 2-CH.sub.35-NHCOCH.sub.3 H " " "" 2-OCH.sub.35-CH.sub.3 " " " "" 2-Cl " " " "" 2-CH.sub.3 " " " "" 2,5-di-Cl " " " "" 2-OCH.sub.35-Cl " " " "6-CH.sub.3 2-OCH.sub.35-CH.sub.3 " " " "" 2,5-di-CH.sub.3 " 4-CH.sub.3 " Na.sup.+ " 3-CH.sub.3 ##STR7## 3-CH.sub.3 " " " 3-CH.sub. 3 ##STR8## 2-CH.sub.3 " " " 3-CH.sub.3 ##STR9## 2,5-di-CH.sub.3 " NH.sub.4.sup.+ " 3-CH.sub.3 CH.sub.2 CH.sub.2 NHSO.sub.2 CH.sub.3 4-OCH.sub.3 " "" 3-CH.sub.3 CH.sub.2 CH.sub.2 CH.sub.2 NHCOCH.sub.3 2-Cl " "6-OCH.sub.3 None CH.sub.3 3-NHCOCH.sub.3 " "" 3-CH.sub.3 CH.sub.2 CH(CH.sub.3).sub.2 3-OCH.sub.3 " "" " CH.sub.2 C.sub.6 H.sub.11 3-Br " "" " CH.sub.2 CH.sub.2 OC.sub.6 H.sub.5 4-Br " "6-Cl " CH(CH.sub.3).sub.2 2,5-di-Cl " "" H CH.sub.2 CH.sub.3 4-C.sub.2 H.sub.5 " K.sup.+" " CH.sub.2 CH.sub.2 OCH.sub.2 CH.sub. 2 OC.sub.2 H.sub.5 4-C.sub.4 H.sub.9n " "5,6-di-Cl 3-CH.sub.3 CH.sub.2 CH.sub.3 2-C.sub.2 H.sub.5 " "6-SO.sub.2 CH.sub.3 " " H 2 "6-CN " " " " "6-CONH.sub.2 " " " " "6-COCH.sub.3 3-NHCOC.sub.6 H.sub.5 " " " "6-COC.sub.6 H.sub.5 3-NHCONHC.sub.2 H.sub.5 " " " "6-COOC.sub.2 H.sub.5 3-NHCOCH.sub.2 OCH.sub.3 " " " "6-SO.sub.2 NH.sub.2 3-NHCOC.sub.6 H.sub.11 " " " "6-SO.sub.2 N(CH.sub.3).sub.2 3-NHCOOC.sub.2 H.sub.5 " " " "6-SO.sub.2 NHC.sub.2 H.sub.4 OCH.sub.3 3-NHCOCH.sub.2 CN " " " "6-NHCOCH.sub.3 " " " " "4-CF.sub.3 None " " " "6-SO.sub.3 C.sub.6 H.sub.5 " " " " "6-OC.sub.2 H.sub.5 3-CH.sub.3 " 2-CH.sub.3 " "" " " 3-CH.sub.3 " "" " " 4-CH.sub.3 " "" " " 2,5-di-CH.sub.3 " "" " " 2-Cl " "6-SCH.sub.3 " " 3-Cl " "6-SCN " " 4-Cl " "6-CH.sub.3 " " 2-OCH.sub.3 " "" " " 3-OCH.sub.3 " "" " " 4-OCH.sub.3 " "" 3-NHCOC.sub.6 H.sub.5 " H 3 "" 3-NHCOOC.sub.2 H.sub.5 " " 4 "" 3-CH.sub.3 " " 5 Na" " " " 6 "__________________________________________________________________________ TABLE 2__________________________________________________________________________ ##STR10##Substituents onRing A (R.sub.1).sub.m R.sub.3 R.sub.4 Z n M__________________________________________________________________________None None CH.sub.3 CH.sub.3 H 1 K.sup.+" " H CH.sub.3 " " "" 7-CH.sub.3 " " " " "" " CH.sub.3 " " " "" 7-CH.sub.3 H CH(CH.sub.3).sub.2 " " "" 7-OCH.sub.3 " CH.sub.3 " " "" 5-OCH.sub.3, 8-CH.sub.3 " " " " "" 5,8-di-OCH.sub.3 " " " " "" 5,8-di-CH.sub.3 " " " " "" 7-Cl " " " " "" 5,8-di-Cl " " " " "6-CH.sub.3 None " " " " "" 5-OCH.sub.3, 8-CH.sub.3 CH.sub.3 " " " Na.sup.+" 7-NHCHO " " " " "" 7-NHCOCH.sub.3 " " " " "" 7-NHCOCH.sub.2 OCH.sub.3 " " H 2 "" 7-NHCOOC.sub.2 H.sub.5 " " " " "" 7-NHCOC.sub.6 H.sub.5 " " " " "" 7-NHCONHC.sub.2 H.sub.5 " " " " K.sup.+" 7-NHCOC.sub.6 H.sub.11 " " " " "6-OCH.sub.3 None " " " " "" 7-CH.sub.3 H " " " "" " " H " " "6-OCH.sub.2 CH.sub.3 " " CH.sub.3 " " "6-SCH.sub.3 " " " " " "6-SCN " " " " " "6-SO.sub.2 NH.sub.2 " " " " " "6-SO.sub.2 NHC.sub.4 H.sub.9n " " " " " "6-SO.sub.2 N(CH.sub.3).sub.2 7-OCH.sub.3 " " " " "6-SO.sub.3 C.sub.6 H.sub.5 7-CH.sub.3 " " " " "6-CN " " " " " "6-CONH.sub.2 " " " " " "4-COOCH.sub.3 " " " " " "6-COCH.sub.3 " " " " " "6-COC.sub.6 H.sub.5 " " " " " "6-Cl None " " " " "5,6-di-Cl " " " 4-CH.sub.3 1 "4-Br " " " 3-CH.sub.3 " "4-CF " " " 2-CH.sub.3 " "6-NHCOCH.sub.3 7-CH.sub.3 " " 4-OCH.sub.3 " "6-SO.sub.2 CH.sub.3 " " " 2-Cl " "6-CH.sub.3 " " " 2,5-di-CH.sub.3 " "" " " " 4-C.sub.4 H.sub.9n " "" " " " 4-CH.sub.3 2 "" " " " H 3 "" " " " " 4 "" " " " " 5 "None " " " " 6 "6-SC.sub.2 H.sub.4 CN " " " " 1 "6-NHCOCH.sub.2 CN " " " " 1 "6-CH.sub.3 " " " 4-CH.sub.3 4 Na.sup.+" " " " 4-Cl 4 "" " " " 4-OCH.sub.3 4 "" " " " 2,5-di-Cl 3 "" " " " 4-CH.sub.3 5 "" " " " 2-Cl 6 "6-COOC.sub.2 H.sub.4 OCH.sub.3 " " " 3-Cl 6 "__________________________________________________________________________ TABLE 3__________________________________________________________________________ ##STR11##Substituents onRing A (R.sub.1).sub.m R.sub.3 Z n M__________________________________________________________________________None None H H 1 Na.sup.+" 6-CH.sub.3 " " " "" " 3-CH.sub.3 " " "" 6-OCH.sub.3 " " " "6-CH.sub.3 " H " " "" 6-CH.sub.3 3-CH.sub.3 " " "4-CH.sub.3 " " " " "4-Cl " " " " "4-CF.sub.3 " " " " "4,7-di-CH.sub.3 " " " " "4,7-di-Cl " " " " "4-OCH.sub.3, 7-Cl " " " " "4-OCH.sub.3, 5-CH.sub.3 " " " " "6-OCH.sub.3 " " " " "" 6-NHCOCH.sub.3 " " " "" 6-NHCOC.sub.6 H.sub.5 " " " "" 6-NHCOC.sub.4 H.sub.9n " " " "" 6-NHCONHC.sub.2 H.sub.5 " " " "" 6-NHCOCH.sub.2 OCH.sub.3 " " " "6-OC.sub.4 H.sub.9n 6-NHCOCH.sub.2 CN " " " "6-SCH.sub.3 6-CH.sub.3 " " " Na.sup.+6-SCN " " " " "6-SO.sub.2 CH.sub.3 " " " " "6-SO.sub.2 NH.sub.2 " " " " "6-SO.sub.2 NHC.sub.2 H.sub.5 " " " " "6-SO.sub.2 N(C.sub.2 H.sub.5).sub.2 " " " " "6-SO.sub.2 NHC.sub.2 H.sub.4 OCH.sub.3 " " " " "6-SO.sub.3 C.sub.6 H.sub.5 " " " " "5,6-di-Cl " " " " "" 6-NHCHO " " " "6-CN 6-CH.sub.3 " " " "6-CONH.sub.2 " " " " "6-COOC.sub.2 H.sub.5 " " " " "6-COCH.sub.3 " " " " "6-COC.sub.6 H.sub.5 " " " " "4-Br6-SO.sub.2 CH.sub.3 " " " " "6-SCH.sub.2 CH.sub.2 CN " " " " "6-SO.sub.2 CH.sub.2 CH.sub.2 CN " " 2-CH.sub.3 " "6-CH.sub.3 " " 2-Cl " "" " " 4-OCH.sub.3 " "" " " 3-CH.sub.3 " "" " " 2,5-di-Cl " "" " " H 2 "" " " " 3 "" " " " 4 "" " " " 5 "" " " " 6 "" " " 2-CH.sub.3 2 "" " " 3-CH.sub.3 2 "" " " 4-CH.sub.3 2 "" " " 2-Cl 3 "" " " 3-Cl 4 "" " " 4-Cl 5 "" " " 4-OCH.sub.3 2 "" " " 4-OC.sub.2 H.sub.5 2 "6-COOCH.sub.2 CH.sub.2 OC.sub.2 H.sub.5 " " 4-OC.sub.4 H.sub.9n 2 "" " " 4-OCH(CH.sub.3).sub.2 2 "__________________________________________________________________________ TABLE 4__________________________________________________________________________ ##STR12##Substituents onRing B (R.sub.1).sub.m R.sub.2 Z n M__________________________________________________________________________6-CH.sub.3 None C.sub.2 H.sub.5 H 1 K.sup.+None " C.sub.6 H.sub.11 " " "" " C.sub.6 H.sub.5 " " "6-CH.sub.3 3CH.sub.3 C.sub.2 H.sub.5 " " "None " CH.sub.2 C.sub.6 H.sub.5 " " "" " CH.sub.2 CH.sub.2 OCH.sub.3 " " "" " CH.sub.2 CH.sub.2 CONH.sub.2 " " "" " CH.sub.2 CH.sub.2 Cl " " "" 3-NHCOCH.sub.3 C.sub.2 H.sub.5 " " "" 2-CH.sub.35-NHCOCH.sub.3 H " " "6-OCH.sub.3 2-OCH.sub.35-CH.sub.3 " " " "" 2-Cl " " " "None 2-CH.sub.3 " " " "" 2,5-di-Cl " " " "" 2-OCH.sub.35-Cl " " " "6-CH.sub.3 2-OCH.sub.35-CH.sub.3 " " " "None 2,5-di-CH.sub.3 " " " Na.sup.+ " 3-CH.sub.3 ##STR13## " " " " 3-CH.sub.3 ##STR14## " " " " 3-CH.sub.3 ##STR15## " " NH.sub.4 " 3-CH.sub.3 ##STR16## " " K.sup.+ " 3-CH.sub.3 CH.sub.2 CH.sub.2 NHSO.sub.2 CH.sub.3 " " "" 3-CH.sub.3 CH.sub.2 CH.sub.2 CH.sub.2 NHCOCH.sub.3 " " "5-Cl None CH.sub.3 " " "5-Br 3-CH.sub.3 CH.sub.2 CH(CH.sub.3).sub.2 " " "6-SO.sub.2 NH.sub.2 " CH.sub.2 C.sub.6 H.sub.11 " " "6-SO.sub.2 NHC.sub.2 H.sub.5 " CH.sub.2 CH.sub.2 OC.sub.6 H.sub.5 " " "6-SO.sub.2 N(CH.sub. 3).sub.2 " CH(CH.sub.3).sub.2 " " "6-SO.sub.2 NHC.sub.3 H.sub.6 OCH.sub.3 H CH.sub.2 CH.sub.3 2-CH.sub.3 1 K.sup.+5-Cl " CH.sub.2 CH.sub.2 OCH.sub.2 CH.sub.2 OC.sub.2 H.sub.5 3-CH.sub.3 " "" 3-CH.sub.3 CH.sub.2 CH.sub.3 4-CH.sub.3 " "" " " 2-Cl " "" " " 3-Cl " "" " " H 2 "None 3-NHCOC.sub.6 H.sub.5 " " " "" 3-NHCONHC.sub.2 H.sub.5 " " " "" 3-NHCOCH.sub.2 OCH.sub.3 " " " "" 3-NHCOC.sub.6 H.sub.11 " " " "" 3-NHCOOC.sub.2 H.sub.5 " " " "" 3-NHCOCH.sub.2 CN " " " "6-SO.sub.2 NHCH.sub.3 " " " " "" None " " 3 "" " " " 4 "None 3-CH.sub.3 " " 5 "" " " " 6 "" " " 2-CH.sub.3 2 "" " " 3-CH.sub.3 3 "" " " 2-Cl 4 "" " " 3-Cl 5 "" " " 4-Cl 6 "__________________________________________________________________________ TABLE 5__________________________________________________________________________ ##STR17##Substituents onRing B (R.sub.1).sub.m R.sub.3 R.sub.4 Z n M__________________________________________________________________________6-CH.sub.3 None CH.sub.3 CH.sub.3 H 1 K.sup.+" " H CH.sub.3 " " "" 7-CH.sub.3 " " " " "" " CH.sub.3 " " " "" 7-CH.sub.3 H CH(CH.sub.3).sub.2 " " "None 7-OCH.sub.3 " CH.sub.3 " " "" 5-OCH.sub.3, 8-CH.sub.3 " " " " "" 5,8-di-OCH.sub.3 " " " " "" 5,8-di-CH.sub.3 " " " " "" 7-Cl " " " " "" 5,8-di-Cl " " " " "" None " " " " Na.sup.+" 5-OCH.sub.3, 8-CH.sub.3 CH.sub.3 " " " "" 7-NHCHO " " " " "" 7-NHCOCH.sub.3 " " " " "" 7-NHCOCH.sub.2 OCH.sub.3 " " " " "" 7-NHCOOC.sub.2 H.sub.5 " " " " "" 7-NHCOC.sub.6 H.sub.5 " " " " "" 7-NHCONHC.sub.2 H.sub.5 " " " " K.sup.+" 7-NHCOC.sub.6 H.sub.11 " " " " "5-Cl None " " " " "" 7-CH.sub.3 H " " " "" " " H " " "" " " CH.sub.3 " " "5-Br " " " " " "6-SO.sub.2 NH.sub.2 " " " " " "6-SO.sub.2 NHC.sub.2 H.sub.5 " " " " " "6-SO.sub.2 N(CH.sub.3).sub.2 " " " " " "6-SO.sub.2 N(CH.sub.3)C.sub.2 H.sub.4 OH 7-OCH.sub.3 " " " " "6-SO.sub.2 NHC.sub.3 H.sub.6 OCH.sub.3 7-CH.sub.3 " " " " "6-OCH.sub.3 " " " " " "" " " " 2-CH.sub.3 " "" " " " 3-CH.sub.3 " "5-Cl " " " 4-CH.sub.3 " "" " " " 2-Cl " "" None " " 3-Cl " "" " " " 4-OCH.sub.3 1 "" " " " 4-OC.sub.4 H.sub.9n " "" " " " 2,5-di-CH.sub.3 " "" 7-CH.sub.3 " " H 2 "" " " " " 3 "None " " " " 4 "" " " " " 5 "" " " " " 6 "__________________________________________________________________________ TABLE 6__________________________________________________________________________ ##STR18##Substituents onRing B (R.sub.1).sub.m R.sub.3 Z n M__________________________________________________________________________None None H H 1 Na.sup.+" 6-CH.sub.3 " " " "6-CH.sub.3 " 3-CH.sub.3 " " "" 6-OCH.sub.3 " " " "None " H " 2 "" 6-CH.sub.3 3-CH.sub.3 " 3 "" " " " 4 "" " " " 5 "" " " " 6 "" " " 2-CH.sub.3 1 "" " " 3-CH.sub.3 2 "" " " 4-CH.sub.3 2 "" " " 2-Cl 1 "" " " 3-Cl 2 "" 6-NHCOCH.sub.3 " 4-Cl 4 K.sup.+" 6-NHCOC.sub.6 H.sub.5 " " 1 "" 6-NHCOC.sub.4 H.sub.9n " " " "" 6-NHCONHC.sub.2 H.sub.5 " " " "5-Br 6-NHCOCH.sub.2 OCH.sub.3 " " " "6-OCH.sub.3 6-NHCOCH.sub.2 CN " " " "6-SO.sub.2 NH.sub.2 6-CH.sub.3 " " " Na.sup.+6-SO.sub.2 NHC.sub.4 H.sub.9 n " " " " "6-SO.sub.2 NHC.sub.3 H.sub.6 OCH.sub.3 " " " " "6-SO.sub.2 N(C.sub.2 H.sub.5).sub.2 " " " " "6-SO.sub.2 N(C.sub.2 H.sub.4 OH).sub.2 " " " " "6-SO.sub.2 NHC.sub.6 H.sub.11 " " " " "6-SO.sub.2 N(CH.sub.3)C.sub.2 H.sub.4 OH " " " " "5-Cl " " " " "" " " " " "" 6-NHCHO " " " "" 6-CH.sub.3 " " " "__________________________________________________________________________ TABLE 7__________________________________________________________________________ ##STR19##Substituents onRing C (R.sub.1).sub.m R.sub.2 Z n M__________________________________________________________________________5-CH.sub.3 None C.sub.2 H.sub.5 H 1 K.sup.+5-Cl " C.sub.6 H.sub.11 " " "5-CH.sub.2 CH(CH.sub.3).sub.2 " C.sub.6 H.sub.5 " " "5-C.sub.6 H.sub.5 3CH.sub.3 C.sub.2 H.sub.5 " " "5-C.sub.6 H.sub.11 " CH.sub.2 C.sub.6 H.sub.5 " " "5-C.sub.6 H.sub.4p-Cl " CH.sub.2 CH.sub.2 OCH.sub.3 " " "5-C.sub.6 H.sub.4 OCH.sub.3 " CH.sub.2 CH.sub.2 CONH.sub.2 " " "5-C.sub.6 H.sub.4m-OCH.sub.3 " CH.sub.2 CH.sub.2 Cl " " "5-SCH.sub.3 3-NHCOCH.sub.3 C.sub.2 H.sub.5 " " "" 2-CH.sub.35-NHCOCH.sub.3 H " " "" 2-OCH.sub.35-CH.sub.3 " " " "" 2-Cl " " " "" 2-CH.sub.3 " " " "" 2,5-di-Cl " " " "" 2-OCH.sub.35-Cl " " " "" 2-OC.sub.2 H.sub.55-CH.sub.3 " " " "5-OC.sub.2 H.sub.5 2,5-di-CH.sub.3 " " " Na.sup.+ 5-SC.sub.2 H.sub.5 3-CH.sub.3 ##STR20## " " " " 3-CH.sub.3 ##STR21## " " " " 3-CH.sub.3 ##STR22## " " NH.sub.4.sup.+ " 3-CH.sub.3 ##STR23## " " K.sup.+ " 3-CH.sub.3 CH.sub.2 CH.sub.2 NHSO.sub.2 CH.sub.3 " " "" 3-CH.sub.3 CH.sub.2 CH.sub.2 CH.sub.2 NHCOCH.sub.3 " " "" None CH.sub.3 " " "5-Cl 3-CH.sub.3 CH.sub.2 CH(CH.sub.3).sub.2 " " "5-SO.sub.2 CH.sub.3 " CH.sub.2 C.sub.6 H.sub.11 " " "5-OC.sub.4 H.sub.9n " CH.sub.2 CH.sub.2 OC.sub.6 H.sub.5 " " "5-SCH.sub.2 CH.sub.2 OH " CH(CH.sub.3).sub.2 " " "5-SCH.sub.2 CH.sub.2 COOCH.sub.3 H CH.sub.2 CH.sub.3 " " K.sup.+ ##STR24## " CH.sub.2 CH.sub.2 OCH.sub.2 CH.sub.2 OC.sub.2 H.sub.5 " " " 5-SCH.sub.2 SC.sub.6 H.sub.5 3-CH.sub.3 CH.sub.2 CH.sub.3 2-CH.sub.3 " "5-SO.sub.2 CH.sub.3 " " 3-CH.sub.3 " "5-SO.sub.2 NH.sub.2 " " 4-CH.sub.3 " "5-SO.sub.2 NHC.sub.2 H.sub.5 " " 2-Cl " "5-SCN 3-NHCOC.sub.6 H.sub.5 " 3-Cl " "5-SO.sub.2 N(CH.sub.3).sub.2 3-NHCONHC.sub.2 H.sub.5 " 4-Cl " "5-SO.sub.3 (C.sub.6 H.sub.5) 3-NHCOCH.sub.2 OCH.sub.3 " 2,5-di-Cl " "5-SCH.sub.2 CHCH.sub.2 3-NHCOC.sub.6 H.sub.11 " 2,5-di-CH.sub.3 " "5-SCH.sub.2 CH.sub.2 OCH.sub.3 3-NHCOOC.sub.2 H.sub.5 " 2-OCH.sub.3 " " ##STR25## 3-NHCOCH.sub.2 CN " 3-NHCOCH.sub.3 " " 5-SC.sub.6 H.sub.11 " " 4-OCH.sub.3 " "5-SC.sub.6 H.sub.5 None " 4-OCH(CH.sub.3).sub.2 " "5-SO.sub.2 C.sub.6 H.sub.5 " " 4-OC.sub.4 H.sub.9n " "5-I 3-CH.sub.3 " H 2 "5-Br " " " 3 " ##STR26## " " " 4 " 5-SCH.sub.2 CH.sub.2 NHSO.sub.2 CH.sub.3 " " " 5 "5-SCH.sub.2 CH.sub.2 NHCOCH.sub.3 " " " 6 "__________________________________________________________________________ TABLE 8__________________________________________________________________________ ##STR27##Substituents onRing C (R.sub.1).sub.m R.sub.3 R.sub.4 Z n M__________________________________________________________________________None None CH.sub.3 CH.sub.3 H 1 K.sup.+" " H CH.sub.3 " " "" 7-CH.sub.3 " " " " "5-CH.sub.3 " CH.sub.3 " " " "5-CH.sub.2 CH.sub.3 7-CH H CH(CH.sub.3).sub.2 " " "5-CH(CH.sub.3).sub.2 7-OCH.sub.3 " CH.sub.3 " " "5-CH.sub.2 CH(CH.sub.3).sub.2 5-OCH.sub.3, 8-CH.sub.3 " " " " "5-C.sub.6 H.sub.5 5,8-di-OCH.sub.3 " " " " "5-C.sub.6 H.sub.11 5,8-di-CH.sub.3 " " " " "5-C.sub.6 H.sub.4o-Cl 7-Cl " " " " "5-C.sub.6 H.sub.4m-CH.sub.3 5,8-di-Cl " " " " "5-C.sub.6 H.sub.4p-OCH.sub.3 None " " " " Na.sup.+5-OC.sub.2 H.sub.5 5-OCH.sub.3, 8-CH.sub.3 CH.sub.3 " " " "" 7-NHCHO " " " " "" 7-NHCOCH.sub.3 " " " " "" 7-NHCOCH.sub.2 OCH.sub.3 " " " " "" 7-NHCOOC.sub.2 H.sub.5 " " " " "" 7-NHCOC.sub.6 H.sub.5 " " " " "" 7-NHCONHC.sub.2 H.sub.5 " " " " K.sup.+5-Cl 7-NHCOC.sub.6 H.sub.11 " " " " "" None " " " " "" 7-CH.sub.3 H " " 2 "" " " H " " "5-I " " CH.sub.3 " " "5-Br " " " " " "5-SO.sub.2 CH.sub.3 " " " " " "5-SO.sub.2 NH.sub.2 " " " " " "5-SO.sub.2 N(CH.sub.3).sub.2 " " " " " "5-SO.sub.2 N(C.sub.2 H.sub.5).sub.2 7-OCH.sub.3 " " " " "5-SO.sub.2 NHC.sub.3 H.sub.6 OCH.sub.3 7-CH.sub.3 " " " " "5-SO.sub.2 CH.sub.2 CH.sub.2 OC.sub.2 H.sub.5 " " " " " "5-SC.sub.6 H.sub.5 " " " " " "5-SC.sub.6 H.sub.11 " " " " " "5-SO.sub.2 C.sub.6 H.sub.5 " " " " " "5-SO.sub.3 C.sub.6 H.sub.5 " " " " " "5-SCH.sub.2 CH.sub.2 OH None " " " " "5-SCH.sub.2 CHCH.sub.2 " " " " " "5-SCH.sub.2 COOC.sub.2 H.sub.5 " " " " " "5-SCH.sub.2 C.sub.6 H.sub.5 " " " " " "5-SCH.sub.2 C.sub.6 H.sub.11 7-CH " " " " "5-SCH.sub.2 CH.sub.2 OC.sub.2 H.sub.5 " " " 2-CH.sub.3 " "5-SCN " " " 3-CH.sub.3 " "5-SCH.sub.2 CH.sub.2 NHCOCH.sub.3 " " " 4-CH.sub.3 " " ##STR28## " " " 2-Cl " " 5-SCH.sub.2 CH.sub.2 OC.sub.6 H.sub.5 " " " 3-Cl " "5-SCH.sub.2 CH.sub.3 " " " 4-OCH " "" " " " 4-C.sub.2 H.sub.5 " "" " " " 4-NHCOCH.sub.3 " "" " " " 4-Br " "" " " " 4-I " "" " " " 2,5-di-CH.sub.3 " Na.sup.+" " " " 2,5-di-Cl " "5-SCH.sub.3 " " " H 2 "" " " " " 3 "" " " " " 4 "" " " " " 5 "5-NHCOCH.sub.3 " " " " 6 "__________________________________________________________________________ TABLE 9__________________________________________________________________________ ##STR29##Substituents onRing C (R.sub.1).sub.m R.sub.3 Z n M__________________________________________________________________________None None H H 1 Na.sup.+" 6-CH.sub.3 " " " "5-Cl " 3-CH.sub.3 " " "5-CH.sub.3 6-OCH.sub.3 " " " "5-CH(CH.sub.3).sub.2 " H " " "5-CH.sub.2 CH(CH.sub.3).sub.2 6-CH.sub.3 3-CH.sub.3 " " "5-C.sub.6 H.sub.5 " " " " "5-C.sub.6 H.sub.4p-Cl " " " " "5-C.sub.6 H.sub.4p-OCH.sub.3 " " " " "5-C.sub.6 H.sub.4m-CH.sub.3 " " " " "5-OC.sub.2 H.sub.5 " " " " "5-OCH(CH.sub.3).sub.2 " " " " "5-C.sub.6 H.sub.11 " " " " "5-SCN " " " " "5-SCH.sub.3 6-NHCOCH.sub.3 " " " K.sup.+5-SCH.sub.2 CH(CH.sub.3).sub.2 6-NHCOC.sub.6 H.sub.5 " " " "5-SCH.sub.2 CHCH.sub.2 6-NHCOC.sub.4 H.sub.9n " " " "5-SC.sub.6 H.sub.11 6-NHCONHC.sub.2 H.sub.5 " " " "5-SC.sub.6 H.sub.5 6-NHCOCH.sub.2 OCH.sub.3 " " " "5-SCH.sub.2 C.sub.6 H.sub.5 6-NHCOCH.sub.2 CN " " " "5-SCH.sub.2 CH.sub.2 OC.sub.6 H.sub.5 6-CH.sub.3 " " " Na.sup.+5-SCH.sub.2 CH.sub.2 OC.sub.2 H.sub.5 " " " " "5-SCH.sub.2 CH.sub.2 OH " " " " "5-SCH.sub.2 CH.sub.2 Cl " " " " "5-SCH.sub.2 COOC.sub.2 H.sub.5 " " " " "5-SCH.sub.2 CH.sub.2 OCOCH.sub.3 " " " " "5-SCH.sub.2 C.sub.6 H.sub.11 " " " " "5-SO.sub.2 CH.sub.3 " " " " "5-SO.sub.2 C.sub.4 H.sub.9n " " " " "5-SO.sub.2 CH.sub.2 CH.sub.2 OCH.sub.3 6-NHCHO " " " "5-SO.sub.2 C.sub.6 H.sub.5 6-CH.sub. 3 " " " "5-SO.sub.2 C.sub.6 H.sub.11 " " " " "5-SO.sub.2 CH.sub.2 C.sub.6 H.sub.5 " " " " "5-SO.sub.2 CH.sub.2 CH.sub.2 OH " " " " " ##STR30## " " " " " 5-SCH.sub.2 CH.sub.2 NHCOCH.sub.3 " " " " " ##STR31## " " " " " 5-SO.sub.2 NH.sub.2 " " " " "5-SO.sub.2 NHC.sub.3 H.sub.6 OCH.sub.3 " " " " "5-SO.sub.2 NH(CH.sub.3).sub.2 " " " " "5-SO.sub.2 NHC.sub.2 H.sub.5 " " " " "5-SO.sub.2 NHC.sub.6 H.sub.11 " " " " "5-SO.sub.3 C.sub.6 H.sub.5 " " " " "5-SO.sub.2 NHC.sub.6 H.sub.5 " " " " "5-NHCOCH.sub.3 " " " " "5-SC.sub.2 H.sub.5 " " 2-CH.sub.3 " "" " " 3-CH.sub.3 " "" " " 4-CH.sub.3 " "" " " 2-Cl " "" " " 4-OCH.sub.3 " "" " " 2,5-di-Cl " "" " " 2,5-di-CH.sub.3 " "" " " H 2 "" " " " 3 "" " " " 4 "" " " " 5 "" " " " 6 "__________________________________________________________________________ TABLE 10__________________________________________________________________________ ##STR32##Substituents onRing D (R.sub.1).sub.m R.sub.2 Z n M__________________________________________________________________________3-CH.sub.3 None C.sub.2 H.sub.5 H 1 K.sup.+" " C.sub.6 H.sub.11 " " "" " C.sub.6 H.sub.5 " " "" 3CH.sub.3 C.sub.2 H.sub.5 " " "" " CH.sub.2 C.sub.6 H.sub.5 " " "" " CH.sub.2 CH.sub.2 OCH.sub.3 " " "" " CH.sub.2 CH.sub.2 CONH.sub.2 " " "3-SCH.sub.3 " CH.sub.2 CH.sub.2 Cl " " "3-C.sub.6 H.sub.5 3-NHCOCH.sub.3 C.sub.2 H.sub.5 " " "3-C.sub.6 H.sub.4p-Cl 2-CH.sub.35-NHCOCH.sub.3 H " " "3-C.sub.6 H.sub.4o-CN 2-OCH.sub.35-CH.sub.3 " " " "" 2-Cl " " " "" 2-CH.sub.3 " " " "" 2,5-di-Cl " " " "" 2-OCH.sub.35-Cl " " " "" 2-OC.sub.2 H.sub.55-CH.sub.3 " " " "" 2,5-di-CH.sub.3 " " " Na.sup.+ 3-C.sub.6 H.sub.5 3-CH.sub.3 ##STR33## " " " " 3-CH.sub.3 ##STR34## " " " " 3-CH.sub.3 ##STR35## " " NH.sub.4.sup.+ " 3-CH.sub.3 ##STR36## " " K.sup.+ " 3-CH.sub.3 CH.sub.2 CH.sub.2 NHSO.sub.2 CH.sub.3 " " "3-C.sub.6 H.sub.4p-CH.sub.3 3-CH.sub.3 CH.sub.2 CH.sub.2 CH.sub.2 NHCOCH.sub.3 " " "3-C.sub.6 H.sub.5 None CH.sub.3 " " "" 3-CH.sub.3 CH.sub.2 CH(CH.sub.3).sub.2 " " "" " CH.sub.2 C.sub.6 H.sub.11 " " "" " CH.sub.2 CH.sub.2 OC.sub.6 H.sub.5 " " "" " CH(CH.sub.3).sub.2 " " "" H CH.sub.2 CH.sub.3 " " K.sup.+" " CH.sub.2 CH.sub.2 OCH.sub.2 CH.sub.2 OC.sub.2 H.sub.5 " " "3-SO.sub.2 CH.sub.3 3-CH.sub.3 CH.sub.2 CH.sub.3 " " "3-SCH.sub.2 CH.sub.2 COOCH.sub.3 " " " " "3-SCH.sub.2 C.sub.6 H.sub.5 " " " " "3-SCH.sub.2 CH.sub.2 OCH.sub.3 " " " " "3-SC.sub.6 H.sub.11 3-NHCOC.sub.6 H.sub.5 " " " "3-SC.sub.2 H.sub.5 3-NHCONHC.sub.2 H.sub.5 " " " "" 3-NHCOCH.sub.2 OCH.sub.3 " " " "" 3-NHCOC.sub.6 H.sub.11 " " " "" 3-NHCOOC.sub.2 H.sub.5 " " " "" 3-NHCOCH.sub.2 CN " " " "3-SCH.sub.2 COOCH.sub.3 " " " " "" None " " 2 "" " " " 3 "" 3-CH.sub.3 " " 4 "3-SCH.sub.3 " " " 5 "" " " " 6 "" " " 2-CH.sub.3 1 "" " " 3-Cl " "3-SCH.sub.2 CH(CH.sub.3).sub.2 " " 4-Cl " "" " " 2,5-di-Cl " "" " " 4-OCH.sub.3 " "__________________________________________________________________________ TABLE 11__________________________________________________________________________ ##STR37##Substituents onRing D (R.sub.1).sub.m R.sub.3 R.sub.4 Z n M__________________________________________________________________________3-CH.sub.3 None CH.sub.3 CH.sub.3 H 1 K.sup.+" " H CH.sub.3 " " "" 7-CH.sub.3 " " " " "" " CH.sub.3 " " " "" 7-CH.sub.3 H CH(CH.sub.3).sub.2 " " "" 7-OCH.sub.3 " CH.sub.3 " " "" 5-OCH.sub.3, 8-CH.sub.3 " " " " "" 5,8-di-OCH.sub.3 " " " " "" 5,8-di-CH.sub.3 " " " " "3-Cl 7-Cl " " " " "3-SCH.sub.3 5,8-di-Cl " " " " "3-C.sub.6 H.sub.5 None " " " " Na.sup.+" 5-OCH.sub.3, 8-CH.sub.3 CH.sub.3 " " " "" 7-NHCHO " " " " "" 7-NHCOCH.sub.3 " " " " "" 7-NHCOCH.sub.2 OCH.sub.3 " " " " "" 7-NHCOOC.sub.2 H.sub.5 " " " " "" 7-NHCOC.sub.6 H.sub.5 " " " " "" 7-NHCONHC.sub.2 H.sub.5 " " " " K.sup.+" 7-NHCOC.sub.6 H.sub.11 " " " " "" None " " " " "" 7-CH.sub.3 H " " " "C.sub.6 H.sub.4o-CN " " H " " "" " " CH.sub.3 " " "" " " " " " "" " " " " " "3-C.sub.6 H.sub.4p-CH.sub.3 " " " " " "3-C.sub.6 H.sub.4o-Cl " " " " " "3-SO.sub.2 CH.sub.3 7-OCH.sub.3 " " " " "3-SC.sub.6 H.sub.11 7-CH.sub.3 " " " " "3-SCH.sub.2 CH.sub.2 OCH.sub.3 " " " " " "3-SCH.sub.2 CH.sub.2 COOCH.sub.3 " " " " " "3-SCH.sub.2 C.sub.6 H.sub.5 " " " " " "3-CH.sub.2 CH.sub.3 " " " " " "3-SCH.sub.2 COOCH.sub.3 " " " " " "3-SCH.sub.2 CH.sub.2 COOC.sub.2 H.sub.5 None " " " " "3-SCH.sub.2 CH.sub.2 COOCH(CH.sub.3).sub.2 " " " " " "3-SO.sub.2 C.sub.4 H.sub.9n " " " " " "3-SCH.sub.2 CH.sub.2 CONHC.sub.4 H.sub.9n " " " " " "3-SCH.sub.3 7-CH.sub.3 " " " " "" " " " 2-CH.sub.3 " "3-SC.sub.2 H.sub.5 " " " 2-Cl " "" " " " 2-OCH.sub.3 " "" " " " 3-Cl " "" " " " 4-Cl " "" " " " 2,5-di-Cl " "" " " " 3-OC.sub.2 H.sub.5 " "" " " " 4-OCH.sub.3 " "" " " " 4-SCH.sub.3 " "" " " " 4-OCH(CH.sub.3).sub.2 " "" " " " 2,5-di-OCH.sub.3 " Na.sup.+" " " " 2,5-di-CH.sub.3 " "" " " " " 2 "" " " " " 3 "" " " " " 4 "" " " " " 5 "" " " " " 6 "__________________________________________________________________________ TABLE 12__________________________________________________________________________ ##STR38##Substituents onRing D (R.sub.1).sub.m R.sub.3 Z n M__________________________________________________________________________3-CH.sub.3 None H H 1 Na.sup.+" 6-CH.sub.3 " " " "" " 3-CH.sub.3 " " "" 6-OCH.sub.3 " " " "" " H " " "3-Cl 6-CH.sub.3 3-CH.sub.3 " " "3-SCH.sub.3 " " " " "3-CH.sub.2 CH.sub.3 " " " " "3-SCH.sub.2 CH.sub.2 OCH.sub. 3 " " " " "3-SCH.sub.2 CH.sub.2 OC.sub.2 H.sub.5 " " " " "3-SCH.sub.2 CH.sub.2 COOCH.sub.3 " " " " "3-SCH.sub.2 COOCH.sub.2 CH.sub.3 " " " " "3-SCH.sub.2 C.sub.6 H.sub.5 " " " " "3-SC.sub.6 H.sub.11 " " " " "3-SCH.sub.3 6-NHCOCH.sub.3 " " " K.sup.+" 6-NHCOC.sub.6 H.sub.5 " " " "" 6-NHCOC.sub.4 H.sub.9n " " " "" 6-NHCONHC.sub.2 H.sub.5 " " " "" 6-NHCOCH.sub.2 OCH.sub.3 " " " "" 6-NHCOCH.sub.2 CN " " " "3-SO.sub.2 CH.sub.3 6-CH.sub.3 " " " Na.sup.+3-SO.sub.2 C.sub.4 H.sub.9n " " " " "3-C.sub.6 H.sub.5 " " " " "3-C.sub.6 H.sub.4o-CN " " " " "3-C.sub.6 H.sub.4o-Cl " " " " "3-C.sub.6 H.sub.4p-CH.sub.3 " " " " "3-C.sub.6 H.sub.4m-CH.sub.3 " " " " "3-C.sub.6 H.sub.4o-CH.sub.3 " " " " "3-C.sub.6 H.sub.4o-CONH.sub.2 " " " " "3-C.sub.6 H.sub.4OCN 6-NHCHO " " " "3-SCH.sub.2 CH.sub.2 OC.sub.6 H.sub.5 6-CH.sub.3 " " " "3-SO.sub. 2 C.sub.4 H.sub.9n " " " " "3-SO.sub.2 CH.sub.2 CH.sub.2 COOCH.sub.3 " " " " "3-SO.sub.2 CH.sub.2 COOCH.sub.3 " " " " "3-SO.sub.2 C.sub.6 H.sub.11 " " " " "3-SO.sub.2 CH.sub.2 CH.sub.3 " " " " "3-SO.sub.2 CH.sub.2 CH.sub.2 OCH.sub.3 " " " " "3-SCH.sub.2 CH.sub.2 CONHC.sub.2 H.sub.4 OH " " 4-CH.sub.3 1 "3-SCH.sub.2 CH.sub.3 " " 3-CH.sub.3 " "" " " 2-Cl " "" " " 4-OCH.sub.3 " "" " " 2,5-di-Cl " "" " " 2,5-di-CH.sub.3 " "" " " 2,5-di-OCH.sub.3 " "" " " H 2 "3-C.sub.6 H.sub.5 " " 2-Cl " "" " " 3-Cl " "" " " 4-Cl " "" " " H 3 "" " " " 4 "" " " " 5 "" " " " 6 "" " " 4-OCH.sub.3 2 "" " " 4-CH.sub.3 " "" " " 4-Br " "" " " 4-I " "" " " 4-NHCOCH.sub.3 " "__________________________________________________________________________ TABLE 13__________________________________________________________________________ ##STR39##Substituents onRing E (R.sub.1).sub.m R.sub.2 Z n M__________________________________________________________________________3-CH.sub.34-Br None C.sub.2 H.sub.5 H 1 K.sup.+" " C.sub.6 H.sub.11 " " "" " C.sub.6 H.sub.5 " " "" 3CH.sub.3 C.sub.2 H.sub.5 " " "" " CH.sub.2 C.sub.6 H.sub.5 " " "" " CH.sub.2 CH.sub.2 OCH.sub.3 " " "" " CH.sub.2 CH.sub.2 CONH.sub.2 " " "" " CH.sub.2 CH.sub.2 Cl " " "" 3-NHCOCH.sub.3 C.sub.2 H.sub.5 " " "" 2-CH.sub.35-NHCOCH.sub.3 H " " "" 2-OCH.sub.35-CH.sub.3 " " " "" 2-Cl " " " "" 2-CH.sub.3 " " " "" 2,5-di-Cl " " " "" 2-OCH.sub.35-Cl " " " "3-CH4-Cl 2-OCH.sub.35-CH.sub.3 " " " "" 2,5-di-CH.sub.3 " " " Na.sup.+ " 3-CH.sub.3 ##STR40## " " " " 3-CH.sub.3 ##STR41## " " " 3-CH.sub.34-CN 3-CH.sub.3 ##STR42## " " NH.sub.4.sup.+ 3-CH.sub.34-COOC.sub.2 H.sub.5 3-CH.sub.3 ##STR43## " " K.sup.+ " 3-CH.sub.3 CH.sub.2 CH.sub.2 NHSO.sub.2 CH.sub.3 " " "" 3-CH.sub.3 CH.sub.2 CH.sub.2 CH.sub.2 NHCOCH.sub.3 " " "" None CH.sub.3 " " "3-CH.sub.34-SCH.sub.2 CHCH.sub.2 3-CH.sub.3 CH.sub.2 CH(CH.sub.3).sub.2 " " "" " CH.sub.2 C.sub.6 H.sub.11 " " "" " CH.sub.2 CH.sub.2 OC.sub.6 H.sub.5 " " "3-CH.sub.34-SO.sub.2 C.sub.2 H.sub.5 " CH(CH.sub.3).sub.2 " " "3-CH.sub.34-SC.sub.6 H.sub.11 H CH.sub.2 CH.sub.3 " " K.sup.+3-CH.sub.34-OC.sub.2 H.sub.5 " CH.sub.2 CH.sub.2 OCH.sub.2 CH.sub.2 OC.sub.2 H.sub.5 " " "3-Cl4-CN 3-CH.sub.3 " " " "3-CH.sub.34-SCN " " " " "3-Br4-COOCH.sub.3 " " " " "3-CH.sub.34-COOC.sub.2 H.sub.5 " " " " "3-CH.sub.34-CONH.sub.2 3-NHCOC.sub.6 H.sub.5 " " " "3-CH.sub.34-CONHC.sub.2 H.sub.4 OH 3-NHCONHC.sub.2 H.sub.5 " " " "3-CH.sub.34-CONHC.sub.4 H.sub.9n 3-NHCOCH.sub.2 OCH.sub.3 " " " "3-CH.sub.34-OC.sub.6 H.sub.5 3-NHCOC.sub.6 H.sub.11 " " " "3-CH.sub.34-OC.sub.6 H.sub.4p-CH.sub.3 3-NHCOOC.sub.2 H.sub.5 " 2-CH.sub.3 " "3-CH.sub.34-SC.sub.6 H.sub.5 3-NHCOCH.sub.2 CN " 3-Cl " "3-CH.sub.34-SCH.sub.2 CH.sub.2 OH " " 4-OCH.sub.3 " "3-CH.sub.34-SCH.sub.2 CH.sub.3 None " 2,5-di-Cl " " ##STR44## " " 2,5-di-OCH.sub.3 " " 3-CH.sub.34-Br 3-CH.sub.3 " H 2 "" " " " 3 "" " " " 4 "" " " " 5 "" " " " 6 "3-CH.sub.34-CONH.sub.2 " " " " "__________________________________________________________________________ TABLE 14__________________________________________________________________________ ##STR45##Substituents onRing E (R.sub.1).sub.m R.sub.3 R.sub.4 Z n M__________________________________________________________________________3-CH.sub.34-Br None CH.sub.3 CH.sub.3 H 1 K.sup.+" " H CH.sub.3 " " "" 7-CH.sub.3 " " " " "" " CH.sub.3 " " " "" 7-CH.sub.3 H CH(CH.sub.3).sub.2 " " "" 7-OCH.sub.3 " CH.sub.3 " " "" 5-OCH.sub.3, 8-CH.sub.3 " " " " "" 5,8-di-OCH.sub.3 " " " " "" 5,8-di-CH.sub.3 " " " " "" 7-Cl " " " " "" 5,8-di-Cl " " " " "3-CH.sub.34-CN None " " " " Na.sup.+" 5-OCH.sub.3, 8-CH.sub.3 CH.sub.3 " " " "" 7-NHCHO " " " " "3-CH.sub.34-COOC.sub.2 H.sub.5 7-NHCOCH " " " " "" 7-NHCOCH.sub.2 OCH.sub.3 " " " " "" 7-NHCOOC.sub.2 H.sub.5 " " " " "3-CH.sub.3 7-NHCOC.sub.6 H.sub.5 " " " " "" 7-NHCONHC.sub.2 H.sub.5 " " " " K.sup.+3-CH.sub.34-Cl 7-NHCOC.sub.6 H.sub.11 " " " " "" None " " " " "" 7-CH.sub.3 H " " " "" " " H " " "3-Cl4-CN " " CH.sub.3 " " "3-Br4-COOCH.sub.3 " " " " " "3-CH.sub.34-COOCH.sub.3 " " " " " "3-CH.sub.34-CONH.sub.2 " " " " " "3-CH.sub.34-CONHC.sub.2 H.sub.4 OH " " " " " "3-CH.sub.34-CONHC.sub.4 H.sub.9n 7-OCH.sub.3 " " " " "3-CH.sub.34-CONHC.sub.3 H.sub.6 OCH.sub.3 7-CH.sub.3 " " " " "3-CH.sub.34-COOC.sub.2 H.sub.4 OCH.sub.3 " " " " " "3-CH.sub.34-SCH.sub.2 CH.sub.2 OH " " " " " "3-CH.sub.34-SCH.sub.2 CH.sub.2 OCOCH.sub.3 " " " " " "3-CH.sub.34-SCH.sub.3 " " " " " "3-CH.sub.34-SO.sub.2 CH.sub.3 " " " " " "3-CH.sub.34-SC.sub.6 H.sub.5 None " " " " "3-CH.sub.34-SC.sub.6 H.sub.4p-C(CH.sub.3).sub.3 " " " 2-CH.sub.3 " "3-CH.sub.34-SC.sub.6 H.sub.4p-Cl " " " 3-CH.sub.3 " " ##STR46## " " " 4-Cl " " ##STR47## 7-CH.sub.3 " " 4-OCH.sub.3 " " ##STR48## " " " 2,5-di-CH.sub.3 " " 3-CH.sub.34-SC.sub.6 H.sub.11 " " " 2,5-di-Cl " "3-CH.sub.34-SCN " " " 4-OC.sub.2 H.sub.5 " "3-CH.sub.34-OC.sub.6 H.sub.5 " " " 2-Cl " "3-CH.sub.34-OC.sub.2 H.sub.5 " " " 4-Br " "3-CH.sub.34-SCH.sub.2 CHCH.sub.2 " " " 4-I " "3-CH.sub.34-Br " " " 4-CH.sub.3 " "" " " " H 2 "" " " " " 3 "" " " " " 4 "" " " " " 5 Na.sup.+" " " " " 6 "__________________________________________________________________________ TABLE 15__________________________________________________________________________ ##STR49##Substituents onRing E (R.sub.1).sub.m R.sub.3 Z n M__________________________________________________________________________3-CH.sub.34-Cl None H " " Na.sup.+" 6-CH.sub.3 " " " "" " 3-CH.sub.3 " " "" 6-OCH.sub.3 " " " "3-Cl4-CN " H " " "" 6-CH.sub.3 3-CH.sub.3 " " "3-CH.sub.3 " " " " "3-CH.sub.34-COOC.sub.2 H.sub.5 " " " " "3-CH.sub.34-CONH.sub.2 " " " " "3-CH.sub.34-CONHC.sub.2 H.sub.4 OH " " " " "3-CH.sub.34-CONHC.sub.4 H.sub.9n " " " " "3-CH.sub.34-CONHC.sub.3 H.sub.6 OCH.sub.3 " " " " "3-CH.sub.34-CO.sub.2 CH.sub.2 CH.sub.2 OCH.sub.3 " " " " "3-CH.sub.34-CONHCH.sub.3 " " " " "3-CH.sub.34-Br 6-NHCOCH " " " K.sup.+" 6-NHCOC.sub.6 H.sub.5 " " " "" 6-NHCOC.sub.4 H.sub.9n " " " "" 6-NHCONHC.sub.2 H.sub.5 " " " "" 6-NHCOCH.sub.2 OCH.sub.3 " " " "" 6-NHCOCH.sub.2 CN " " " "3-CH.sub.34-SC.sub.2 H.sub.5 6-CH.sub.3 " " " Na.sup.+3-CH.sub.34-SCH.sub.2 CH.sub.2 OH " " " " "3-CH.sub.34-SCH.sub.2 CHCH.sub.2 " " " " "3-CH.sub.34-SCH.sub.2 CH.sub.2 OCOCH.sub.3 " " " " "3-CH.sub.34-SC.sub.6 H.sub.5 " " " " "3-CH.sub.34-SC.sub.6 H.sub.4p-C(CH.sub.3).sub.2 " " " " "3-CH.sub.34-SC.sub.6 H.sub.11 " " " " "3-CH.sub.34-SO.sub.2 CH.sub.2 CH.sub.2 OH " " " " "3-CH.sub.34-SO.sub.2 CH.sub.2 CH.sub.3 " " " " "3-CH.sub.34-OC.sub.6 H.sub.5 6-NHCHO " " " "3-CH.sub.34-OC.sub.6 H.sub.4p-OCH.sub.3 6-CH.sub.3 " " " " ##STR50## " " " " " ##STR51## " " " " " ##STR52## " " " " " 3-CH.sub.34-SCH.sub.2 CH(OH)CH.sub.2 OH " " " " "3-CH.sub.34-SCH.sub.2 COOCH.sub.3 " " " " "3-CH.sub.34-OC.sub.2 H.sub.5 " " " " "3-CH.sub.3 4-Br " " " 2 "" " " " 3 "" " " " 4 "" " " " 5 "" " " " 6 "" " " 2-CH.sub.3 6 "" " " 3-CH.sub.3 6 "" " " 4-CH.sub.3 6 "" " " 4-Cl 1 "" " " 3,4-di-Cl " "" " " 2,5-di-OCH.sub.3 " "" " " 2,5-di-CH.sub.3 " "" " " 4-OCH.sub.3 " "" " " 4-SCH.sub.3 " "" " " 4-OC.sub.2 H.sub.5 " "" " " 4-Br " "" " " 4-I " "__________________________________________________________________________ TABLE 16__________________________________________________________________________ ##STR53## Substituents onA Ring F (R.sub.1).sub.m R.sub.2 Z n M__________________________________________________________________________H 4-CN None C.sub.2 H.sub.5 H 1 K.sup.+" " " C.sub.6 H.sub.11 " " "" " " C.sub.6 H.sub.5 " " "" " 3-CH.sub.3 C.sub.2 H.sub.5 " " "" " " CH.sub.2 C.sub.6 H.sub.5 " " "" " " CH.sub.2 CH.sub.2 OCH.sub.3 " " "" " " CH.sub.2 CH.sub.2 CONH.sub.2 " " "" " " CH.sub.2 CH.sub.2 Cl " " "" " 3-NHCOCH.sub.3 C.sub.2 H.sub.5 " " "" " 2-CH.sub.35-NHCOCH.sub.3 H " " "" " 2-OCH.sub.35-CH.sub.3 " " " "" " 2-Cl " " " "" " 2-CH.sub.3 " " " "" " 2,5-di-Cl " " " "" " 2-OCH.sub.35-Cl " " " "" " 2-OC.sub.2 H.sub.55-CH.sub.3 " " " "C.sub.6 H.sub.5 3-SC.sub.2 H.sub.54-CN 2,5-di-CH.sub. 3 " " " Na.sup.+ " 3-SC.sub.2 H.sub.54-COOCH.sub.3 3-CH.sub.3 ##STR54## " " " " 3-SC.sub.2 H.sub.54-CONH.sub.2 3-CH.sub.3 ##STR55## " " " " 3-SCH.sub.34-CN 3-CH.sub.3 ##STR56## " " NH.sub.4.sup.+ " " 3-CH.sub.3 ##STR57## " " K.sup.+ " " 3-CH.sub.3 CH.sub.2 CH.sub.2 NHSO.sub.2 CH.sub.3 " " "" " 3-CH.sub.3 CH.sub.2 CH.sub.2 CH.sub.2 NHCOCH.sub.3 " " "SO.sub.2 C.sub.6 H.sub.5 " None CH.sub.3 " " "COCH.sub.3 4-CN 3-CH.sub.3 CH.sub.2 CH(CH.sub.3).sub.2 " " "H " " CH.sub.2 C.sub.6 H.sub.11 " " "" " " CH.sub.2 CH.sub.2 OC.sub.6 H.sub.5 " " "" " " CH(CH.sub.3).sub.2 " " "COOC.sub.2 H.sub.5 " H CH.sub.2 CH.sub.3 " " K.sup.+H " " CH.sub.2 CH.sub.2 OCH.sub.2 CH.sub.2 OC.sub.2 H.sub.5 " " "CH.sub.3 4-CN 3-CH.sub.3 CH.sub.2 CH.sub.3 " " "" 4-COOCH.sub.3 " " " " "" 4-CONH.sub.2 " " " " "CH.sub.2 CH.sub.3 4-CN " " " " "C.sub.2 H.sub.5 " 3-NHCOC.sub. 6 H.sub.5 " " " "" 4-COOCH.sub.3 3-NHCONHC.sub.2 H.sub.5 " " " "C.sub.6 H.sub.4p-Cl " 3-NHCOCH.sub.2 OCH.sub.3 " " " "C.sub.6 H.sub.4o-CH.sub.3 " 3-NHCOC.sub.6 H.sub.11 " " " "C.sub.6 H.sub.5 " 3-NHCOOC.sub.2 H.sub.5 " " " "" " 3-NHCOCH.sub.2 CN " " " "H 4-CONHC.sub.2 H.sub.4 OH " " " " "" 4-CONHC.sub.4 H.sub.9n None " " " "" 4-COOC.sub.2 H.sub.4 OCH.sub.3 " " " " "" 4-CONHC.sub.3 H.sub.6 OCH.sub.3 3-CH.sub.3 " " " "" 4-CN " " 2-CH.sub.3 " "" " " " 3-CH.sub.3 " "" " " " 4-CH.sub.3 " "" " " " 4-Cl 2 "SO.sub.2 CH.sub.3 4-CN " " 2-Cl 3 "SO.sub.2 C.sub.6 H.sub.5 " " " 2,5-di-Cl 4 "SO.sub.2 CH.sub.2 CH.sub.3 " " " 2,5-di-CH.sub.3 5 "H " " " 4-OCH.sub.3 6 "__________________________________________________________________________ TABLE 17__________________________________________________________________________ ##STR58## Substituents onA Ring F (R.sub.1).sub.m R.sub.3 R.sub.4 Z n M__________________________________________________________________________H 4-CN None CH.sub.3 CH.sub.3 H 1 K.sup.+" " " H CH.sub.3 " " "" " 7-CH.sub.3 " " " " "" " " CH.sub.3 " " " "" " 7-CH.sub.3 H CH(CH.sub.3).sub.2 " " "" " 7-OCH.sub.3 " CH.sub.3 " " "" " 5-OCH.sub.3, 8-CH.sub.3 " " " " "" " 5,8-di-OCH.sub.3 " " " " "" " 5,8-di-CH.sub.3 " " " " "" " 7-Cl " " " " "" " 5,8-di-Cl " " " " "CH.sub.3 " None " " " " Na.sup.+" " 5-OCH.sub.3, 8-CH.sub.3 CH.sub.3 " " " "H 4-COOCH.sub.3 7-NHCHO " " " " "H 4-COOC.sub.2 H.sub.5 7-NHCOCH.sub.3 " " " " "H 4-COOC.sub.2 H.sub.4 OCH.sub.3 7-NHCOCH.sub.2 OCH.sub.3 " " " " "H 4-CONH.sub.2 7-NHCOOC.sub.2 H.sub.5 " " " " "H 4-CONHC.sub.2 H.sub.5 7-NHCOC.sub.6 H.sub.5 " " " " "" " 7-NHCONHC.sub.2 H.sub.5 " " " " K.sup.+" " 7-NHCOC.sub.6 H.sub.11 " " " " "C.sub.6 H.sub.5 4-CN None " " " " "" " 7-CH.sub.3 H " " " "C.sub.6 H.sub.4p-Cl " " " H " " "C.sub.6 H.sub.4p-CH.sub.3 " " " CH " " "SO.sub.2 CH.sub.3 " " " " " " "" 4-COOCH.sub.3 " " " " " "SO.sub.2 C.sub.6 H.sub.5 " " " " " " "" 4-CN " " " " " "" 4-CONHC.sub.2 H.sub.4 OH 7-OCH.sub.3 " " " " "" 4-COOCH(CH.sub.3).sub.2 7-CH.sub.3 " " " " "CH.sub.3 3-SC.sub.2 H.sub.5 -4-CN " " " " " "C.sub.6 H.sub.5 " " " " " " "" 3-SC.sub.2 H.sub.54-COOCH.sub.3 " " " " " "" 3-SCH.sub.34-COOC.sub.2 H.sub.5 " " " " " "" 3-SO.sub.2 CH.sub.34-COOCH.sub.3 " " " " " "" 3-SC.sub.6 H.sub.54-COOCH.sub.3 None " " " "COCH.sub.3 4-CN " " " " " "" 4-COOCH.sub.3 " " " " " "CH.sub.2 CH.sub.2 OH " " " " " " "H 3-CH.sub.2 CN4-CN 7-CH.sub.3 " " " 2 "H 3-CH.sub.2 CONH.sub.24-CN " " " " " "H 4-CN " " " " " "" 41 " " " " 1 "" " " " " 2-CH.sub.3 " "" " " " " 3-Cl " "" " " " " 3-CH.sub.3 " "" " " " " 4-OCH.sub.3 " "" " " " " 4-OC.sub.4 H.sub.9n " "" " " " " 2,5-di-Cl " "" " " " " 2,5-di-CH.sub.3 " "" " " " " 4-Br " Na.sup.+" " " " " 4-I " "" " " " " H 2 "" " " " " " 3 "" " " " " " 4 "" " " " " " 5 "" " " " " " 6 "__________________________________________________________________________ TABLE 18__________________________________________________________________________ ##STR59## SubstituentsA on Ring F (R.sub.1).sub.m R.sub.3 Z n M__________________________________________________________________________H 4-CN None H H 1 Na.sup.+" " 6-CH.sub.3 " " " "CH.sub.3 " " 3-CH.sub.3 " " "" 4-COOCH.sub.3 6-OCH.sub.3 " " " "" 4-COOC.sub.2 H.sub.4 OC.sub.2 H.sub.5 " H " " "" 4-CONH.sub.2 6-CH.sub.3 3-CH.sub.3 " " "" 4-CONHC.sub.2 H.sub.4 OH " " " " "" 4-CONHC.sub.3 H.sub.6 OCH.sub.3 " " " " "" 4-CONHC.sub.2 H.sub.4 NHCOCH.sub.3 " " " " "CH.sub.2 CH.sub.3 4-CN " " " " "C.sub.6 H.sub.5 " " " " " "" 4-COOCH.sub.2 CH.sub.3 " " " " "" 4-CONH.sub.2 " " " " "C.sub.6 H.sub.4o-Cl " " " " " "H " 6-NHCOCH.sub.3 " " " "" 4-COOCH.sub.3 6-NHCOC.sub.6 H.sub.5 " " " "" " 6-NHCOC.sub.4 H.sub.9n " " " "" 4-CONHC.sub.4 H.sub.9n 6-NHCONHC.sub.2 H.sub.5 " " " "" " 6-NHCOCH.sub.2 OCH.sub.3 " " " "" " 6-NHCOCH.sub.2 CN " " " "SO.sub.2 CH.sub.3 4-CN 6-CH " " " Na.sup.+" 4-COOCH.sub.3 " " " " "H 3-CH.sub.2 CN4-CN " " " " "C.sub.6 H.sub.5 3-SCH.sub.34-CN " " " " "" 3-SCH.sub.2 CH.sub.34-CN " " " " "" 3-SCH.sub.2 CH.sub.34-COOCH.sub.3 " " " " "" 3-SCH.sub.34-CONHC.sub.4 H.sub.9 -n " " " " "SO.sub.2 C.sub.6 H.sub.5 4-CN " " " " "" 4-COOCH.sub.3 " " " " "SO.sub.2 C.sub.6 H.sub.4p-CH.sub.3 4-CN 6-NHCHO " " " "SO.sub.2 C.sub.4 H.sub.9n " 6-CH.sub.3 " " " "COCH.sub.3 " " " " " "COOC.sub.2 H.sub.5 " " " " " "CH.sub.2 CH.sub.2 OH " " " " " "C.sub.6 H.sub.4O-CH.sub.3 " " " " " "" 4-COOCH.sub.3 " " " " "" 4-COOCH(CH.sub.3).sub.2 " " " " "SO.sub.2 C.sub.6 H.sub.11 " " " " " "H 4-CN " " " " "" " " " " 2 "" " " " " 3 "" " " " " 4 "" " " " " 5 "" " " " " 6 "" " " " 2-CH.sub.3 1 "C.sub.6 H.sub.5 " " " 2-Cl " "" " " " 2-OCH.sub.3" " " " 4-OCH.sub.3 " "" " " " 4-Cl " "" " " " 4-CH.sub.3 " "" " " " 4-Cl 2 "" " " " " 3 "" " " " " 4 "" " " " " 5 "" " " " " 6 "" " " " 2,5-di-Cl " "" " " " 2,5-di-CH.sub.3 " "__________________________________________________________________________ TABLE 19__________________________________________________________________________ ##STR60##Substituents onRing G (R.sub.1).sub.m R.sub.2 Z n M__________________________________________________________________________3,5-di-CN4-CH.sub.3 None C.sub.2 H.sub.5 H 1 K.sup.+" " C.sub.6 H.sub.11 " " "" " C.sub.6 H.sub.5 " " "" 3-CH.sub.3 C.sub.2 H.sub.5 " " "3-CN5-C.sub.6 H.sub.5 " CH.sub.2 C.sub.6 H.sub.5 " " "3-COOCH.sub.35-C.sub.6 H.sub.5 " CH.sub.2 CH.sub.2 OCH.sub.3 " " "3-CONH.sub.25-C.sub.6 H.sub.5 " CH.sub.2 CH.sub.2 CONH.sub.2 " " "3-CONHC.sub.2 H.sub.55-C.sub.6 H.sub.5 " CH.sub.2 CH.sub.2 Cl " " "3-COOCH.sub.3 3-NHCOCH.sub.3 C.sub.2 H.sub.5 " " "3-CN 2-CH.sub.35-NHCOCH.sub.3 H " " "3-CN4-CH.sub.35-COOC.sub.2 H.sub.5 2-OCH.sub.35-CH.sub.3 " " " "" 2-Cl " " " "" 2-CH.sub.3 " " " "" 2,5-di-Cl " " " "3-CN4-CH.sub.35-COCH.sub.3 2-OCH.sub.35-Cl " " " "3-COOCH.sub.34-CH.sub.35-CN 2-OCH.sub.35-CH.sub.3 " " " "3-COOCH.sub.34-CH.sub.35-COC.sub.6 H.sub.5 2,5-di-CH.sub.3 " " " Na.sup.+ 3-COOCH.sub.35-COC.sub.6 H.sub.5 3-CH.sub.3 ##STR61## " " " 3-COOCH.sub.35-COCH(CH.sub.3).sub.2 3-CH.sub.3 ##STR62## " " " " 3-CH.sub.3 ##STR63## " " NH.sub.4.sup.+ " 3-CH.sub.3 ##STR64## " " K.sup.+ " 3-CH.sub.3 CH.sub.2 CH.sub.2 NHSO.sub.2 CH.sub.3 " " "" 3-CH.sub.3 CH.sub.2 CH.sub.2 CH.sub.2 NHCOCH.sub.3 " " "" None CH.sub.3 " " "3-SO.sub.2 C.sub.6 H.sub.5 5-COCH 3-CH.sub.3 CH.sub.2 CH(CH.sub.3).sub.2 " " "3-SO.sub.2 CH.sub.35-CN " CH.sub.2 C.sub.6 H.sub.11 " " "3-SO.sub.2 C.sub.6 H.sub.55-Br " CH.sub.2 CH.sub.2 OC.sub.6 H.sub.5 " " "3,5-di-SO.sub.2 CH.sub.3 " CH(CH.sub.3).sub.2 " " "3,5-di-SO.sub.2 NH.sub.2 H CH.sub.2 CH.sub.3 " " K.sup.+3,5-di-SO.sub.2 N(C.sub.2 H.sub.5).sub.2 " CH.sub.2 CH.sub.2 OCH.sub.2 CH.sub.2 OC.sub.2 H.sub.5 " " "3-CN5-COCH.sub.3 3-CH.sub.3 Ab,4 CH.sub.2 CH.sub.3 " " "3-CN5-COOC(CH.sub.3).sub.2 " " " " "3-CN5-COOC.sub.2 H.sub.5 " " " " "3-CONH.sub.25-COOC.sub.2 H.sub.5 " " " " "3-CONH.sub.25-COCH(CH.sub.3).sub.2 3-NHCOC.sub.6 H.sub.5 " " " "3-CONHC.sub.2 H.sub.4 OH5-COCH(CH.sub.3).sub.2 3-NHCONHC.sub.2 H.sub.5 " " " "" 3-NHCOCH.sub.2 OCH.sub.3 " " " "" 3-NHCOC.sub.6 H.sub.11 " " " "" 3-NHCOOC.sub.2 H.sub.5 " " " "" 3-NHCOCH.sub.2 CN " " " "3-CONHC.sub.3 H.sub.6 OCH.sub.35-COCH(CH.sub.3).sub.2 " " 2-CH.sub.3 " "3-CONHC.sub.4 H.sub.9n-5-COCH(CH.sub.3).sub.2 None " 2-Cl " "3-CONHC.sub.2 H.sub.4 OH5-COCH(CH.sub.3).sub.2 " " 4-OCH.sub.3 " "3-COOCH.sub.35-SO.sub.2 CH.sub.3 3-CH.sub.3 " 2,5-di-Cl " "3-CONHC.sub.2 H.sub.55-SO.sub.2 CH.sub.3 " " 2,5-di-CH.sub.3 " "3-CONH.sub.25-SO.sub.2 CH.sub.3 " " 4-Cl " "3-CONH.sub.25-SO.sub.2 C.sub.4 H.sub.9 -n " " 4-Br " "3-COOCH.sub.34-CH.sub.35-SCN " " H 2 "3-CHO4-CH.sub.3 " " " 3 "3-CONH.sub.25-C.sub.6 H.sub.4p-CH.sub.3 " " " 4 "3-CN5-COOC.sub.2 H.sub.5 " " " 5 "3-COOCH.sub.35-COCH(CH.sub.3).sub.2 " " " 6 "__________________________________________________________________________ TABLE 20__________________________________________________________________________ ##STR65##Substituents onRing G (R.sub.1).sub.m R.sub.3 R.sub.4 Z n M__________________________________________________________________________3-CONHC.sub.2 H.sub.55-COCH(CH.sub.3).sub.2 None CH.sub.3 CH.sub.3 H 1 K.sup.+" "H CH.sub.3 " " "3-CONH.sub.25-COCH(CH.sub.3).sub.2 7-CH.sub.3 " " " " "" " CH.sub.3 " " " "" 7-CH.sub.3 H CH(CH.sub.3).sub.2 " " "" 7-OCH.sub.3 " CH.sub.3 " " "" 5-OCH.sub.3, 8-CH.sub.3 " " " " "" 5,8-di-OCH.sub.3 " " " " "" 5,8-di-CH.sub.3 " " " " "" 7-Cl " " " " "" 5,8-di-Cl " " " " "3-COOCH.sub.35-COCH(CH.sub.3).sub.2 None " " " " Na.sup.+" 5-OCH.sub.3, 8-CH.sub.3 CH.sub.3 " " " "" 7-NHCHO " " " " "" 7-NHCOCH.sub.3 " " " " "" 7-NHCOCH.sub.2 OCH.sub.3 " " " " "3,5-di-CN4-CH.sub.3 7-NHCOOC.sub.2 H.sub.5 " " " " "" 7-NHCOC.sub.6 H.sub.5 " " " " "" 7-NHCONHC.sub.2 H.sub.5 " " " " K.sup.+" 7-NHCOC.sub.6 H.sub.11 " " " " "" None " " " " "3-CONH.sub.25-C.sub.6 H.sub.5 7-CH.sub.3 H " " " "" " " H " " "3-COOCH.sub.35-C.sub.6 H.sub.5 " " CH.sub.3 " " "3-COOCH.sub.35-COCH.sub.3 " " " " " "3-CN5-COOC.sub.2 H.sub.5 " " " " " "3-CN4-CH.sub.35-COOC.sub.2 H.sub.5 " " " " " "3-CN4-CH.sub.35-COCH.sub.3 " " " " " "3-COOCH.sub.34-CH.sub.35-CN 7-OCH.sub.3 " " " " "3-CN4-CH.sub.35-CO.sub.2 CH.sub.2 CH.sub.2 OC.sub.2 H.sub.5 7-CH.sub.3 " " " " "3-SO.sub.2 C.sub.6 H.sub.55-COCH.sub.3 " " " " " "3-SO.sub.2 C.sub.6 H.sub.4p-Cl5-COCH.sub.3 " " " " " "3-SO.sub.2 CH.sub.35-CN " " " " " "3-COOCH.sub.35-Br " " " " " "3-COOCH.sub.35-SCN " " " " " "3-CONHC.sub.2 H.sub.4 OH5-COCH(CH.sub.3).sub.2 None " " " " "3-CONHC.sub.3 H.sub.6 OCH.sub.35-COCH(CH.sub.3).sub.2 " " " " " "3-CN5-SO.sub.2 CH.sub.3 " " " " " "3,5-di-SO.sub.2 NH.sub.2 " " " " " "3,5-di-SO.sub.2 NHC.sub.2 H.sub.5 7-CH.sub.3 " " " " "3-COOCH.sub.35-COC.sub.6 H.sub.5 " " " " " "3-CONHC.sub.4 H.sub.9n-5-COC.sub.6 H.sub.5 " " " " " "3-COOCH.sub.35-SO.sub.2 CH.sub.3 " " " " " "3-CONHC.sub.2 H.sub.4 OH5-SO.sub.2 CH.sub.3 " " " " " "3-CHO " " " " " "3-SO.sub.2 C.sub.6 H.sub.5 " " " " " "3-CONHC.sub.2 H.sub.55-COCH(CH.sub.3).sub.2 " " " 2-Cl " "" " " " 2-CH.sub.3 " "" " " " 3-CH.sub.3 " "" " " " 4-OCH.sub.3 " "" " " " 2,5-di-CH.sub.3 " Na.sup.+" " " " 2,5-di-Cl " "" " " " H 2 "" " " " " 3 "" " " " " 4 "3-COOCH.sub.34CH.sub.35-CONH.sub.2 " " " " 5 "" 41 " " " 6 "__________________________________________________________________________ TABLE 21__________________________________________________________________________ ##STR66##Substituents onRing G (R.sub.1).sub.m R.sub.3 Z n M__________________________________________________________________________3-COOCH.sub.35-COCH(CH.sub.3).sub.2 None H H 1 Na.sup.+3-CONH.sub.25-COCH(CH.sub.3).sub.2 6-CH.sub.3 " " " "3-CN5-COCH(CH.sub.3).sub.2 " 3-CH.sub.3 " " "" 6-OCH.sub.3 " " " "3-CONH.sub.25-C.sub.6 H.sub.5 " H " " "" 6-CH.sub.3 3-CH.sub.3 " " "" " " " " "3-CN5-C.sub.6 H.sub.5 " " " " "3-CONHC.sub.2 H.sub.4 OH5-C.sub.6 H.sub.5 " " " " "3-CONHC.sub.2 H.sub.55-COC.sub.6 H.sub.5 " " " " "3-CONHCH.sub.35-COC.sub.6 H.sub.5 " " " " "3-CNCH.sub.35-COOC.sub.2 H.sub.5 " " " " "3-CNCH.sub.35-COOC.sub.2 H.sub.4 OCH.sub.3 " " " " "3-CHO4,5-di-CH.sub.3 " " " " "3-CN4-CH.sub.35-SCH.sub.3 6-NHCOCH.sub.3 " " " K.sup.+3-COOCH.sub.34-CH.sub.35-CONH.sub.2 6-NHCOC.sub.6 H.sub.5 " " " "3-CONH.sub.24-CH.sub.35-CN 6-NHCOC.sub.4 H.sub.9 -n " " " "3,5-di-CN4-CH.sub.3 6-NHCONHC.sub.2 H.sub.5 " " " "" 6-NHCOCH.sub.2 OCH.sub.3 " " " "" 6-NHCOCH.sub.2 CN " " " "" 6-CH.sub.3 " " " Na.sup.+3-CONH.sub.24-CH.sub.35-COOCH.sub.3 " " " " "3-SO.sub.2 CH.sub.35-COCH.sub.3 " " " " "3-SO.sub.2 C.sub.6 H.sub.55-COCH.sub.3 " " " " "3-SO.sub.2 C.sub.6 H.sub.4p-Cl5-COCH.sub.3 " " " " "3-SO.sub.2 CH.sub.35-Br " " " " "3,5-di-SO.sub.2 CH.sub.3 " " " " "3,5-di-SO.sub.2 NH.sub.2 " " " " "3,5-di-SO.sub.2 NHC.sub.2 H.sub.5 " " " " "3-CONHC.sub.2 H.sub.4 OH 5-COCH(CH.sub.3).sub.2 6-NHCHO " " " "3-CONHC.sub.3 H.sub.6 OCH.sub.35-COCH(CH.sub.3).sub.2 6-CH.sub.3 " " " "3-CONHC.sub.2 H.sub.4 NHCOCH.sub.3 " " " " "3-CONHC.sub.4 H.sub.9n-5-C.sub.6 H.sub.5 " " " " "3-CN5-COOC.sub.2 H.sub.5 " " " " "3-CN4-CH.sub.35-COOCH(CH.sub.3).sub.2 " " " " "3-CN4-CH.sub.35-CONHC.sub.2 H.sub.5 " " " " "3-CN4-CH.sub.35-CONHC.sub.6 H.sub.5 " " " " "3-CONH.sub.25-SO.sub.2 CH.sub.3 " " " " "3-CONH.sub.25-COCH(CH.sub.3).sub.2 " " " " "" " " 2-CH.sub.3 " "" " " 3-CH.sub.3 " "" " " 4-CH.sub.3 " "" " " 4-Cl " "" " " 4-OCH.sub.3 " "3-CONHC.sub.2 H.sub.55-COCH(CH.sub.3).sub.2 " " 4-Br " "" " " 2-CH.sub.3 " "" " " 3-Cl " "" " " 4-OCH.sub.3 " "" " " 2,5-di-CH.sub.3 " "" " " 2,5-di-Cl " "" " " 4-Br " "" " " 4-I " "" " " H 2 "" " " " 3 "" " " " 4 "" " " " 5 "" " " " 6 "__________________________________________________________________________ TABLE 22__________________________________________________________________________ ##STR67##Substituents onRing H (R.sub.1).sub.m R.sub.2 Z n M__________________________________________________________________________None None C.sub.2 H.sub.5 H 1 Na.sup.+4-CH.sub.3 " " " " "4-CH.sub.35-CN " " " " "5-CN " " " " "5-CHO 3-CH.sub.3 " " " "4-C.sub.6 H.sub.55-CHO " CH.sub.3 " " "" 2,5-di-CH.sub.3 H " " "4-C.sub.6 H.sub.55-CN 3-Cl " " " "5-SCN 3-CH.sub.3 CH.sub.2 CH.sub.2 CH.sub.2 CH.sub.3 " " "5-COOCH.sub.3 " CH.sub.2 CH.sub.2 OCH.sub.3 " " "" " CH.sub.2 CH.sub.2 CN " " "" " CH.sub.2 CH.sub.2 Cl " " "" " CH.sub.2 CH.sub.2 CONH.sub.2 " " "" " C.sub.6 H.sub.5 " " "" " C.sub.6 H.sub.11 " " "" " CH.sub.2 CH.sub.2 OH " " "" " CH.sub.2 CH.sub.2 C.sub.6 H.sub.5 " " "" " CH.sub.2 CH.sub.2 COOCH.sub.3 " " "5-CONH.sub.2 None C.sub.2 H.sub.5 " " "5-CONHC.sub.2 H.sub. 5 " " " " "5-CON(C.sub.2 H.sub.5).sub.2 " " " " "5-CONHC.sub.2 H.sub.4 OH " " " " H.sup.305-CO.sub.2 C.sub.2 H.sub.5 " " " " "5-CO.sub.2 C.sub.4 H.sub.9n " " " " "5-SCH.sub.3 " " " " "5-SC.sub.2 H.sub.4 OH " " " " "5-SO.sub.2 CH.sub.3 " " " " NH.sub.4.sup.+5-SO.sub.2 CH.sub.2 CH.sub.2 OH " " " " "5-SO.sub.2 NH.sub.2 " " " " "5-SO.sub.2 NHC.sub.2 H.sub.4 OH " " " " "5-SO.sub.2 N(C.sub.2 H.sub.5).sub.2 " " " " "5-SO.sub.2 NHC.sub.6 H.sub.11 " " " " "5-SO.sub.2 C.sub.6 H.sub.5 " " " " "4-CH.sub.2 Cl " " " " "4-CF.sub.3 " " " " "4-CH.sub.35-COCH.sub.3 " " " " Na.sup.+5-COC.sub.6 H.sub.5 " " " " "5-COCH.sub.3 " " " " "5-NNC.sub.6 H.sub.5 " " " " "5-Br " " " " "4-CH.sub.35-COOC.sub.2 H.sub.5 3-CH.sub.3 CH.sub.3 " " K.sup.+" None C.sub.4 H.sub.9n 2-CH.sub.3 " "" " C.sub.2 H.sub.5 3-CH.sub.3" " " 4-Cl " "" " " 2,5-di-Cl " "" " " 2,5-di-CH.sub.3 " "" " " 4-OCH.sub.3 " "" " " 4-Br " "" " " 4-I " "4-CH.sub.35-COOCH.sub.3 " " 4-CH.sub.3 2 "" " " 2-Cl 3 "" " " 3-Cl 4 "" " " H 2 "" " " " 3 "" " " " 4 "" " " " 5 "" " " " 6 "__________________________________________________________________________ TABLE 23__________________________________________________________________________ ##STR68##Substituents onRing H (R.sub.1).sub.m R.sub.3 R.sub.4 Z n M__________________________________________________________________________None None H CH.sub.3 H 1 Na.sup.+4-CH.sub.3 7-CH.sub.3 " " " " "4-C.sub.6 H.sub.5 " " " " " "4-CF.sub.3 " " " " " "5-CONH.sub.2 " " " " " "5-CON(C.sub.2 H.sub.5).sub.2 " " " " " "5-CN " " " " " "5-SCN " " " " " "5-CO.sub.2 CH.sub.3 " " " " " "5-CO.sub.2 C.sub.2 H.sub.4 OCH.sub.3 " " " " " "5-CHO " " " " " "4-C.sub.6 H.sub.55-CHO " " " " " "5-SC.sub.4 H.sub.9n " " " " " "5-SO.sub.2 C.sub.4 H.sub.9n " " " " " "5-SO.sub.2 NH.sub.2 " " " " " "5-SO.sub.2 NHC.sub.2 H.sub.4 OH " " " " " "5-SO.sub.2 N(C.sub.2 H.sub.5).sub.2 " " " " " "5-SO.sub.2 NHC.sub.6 H.sub.5 " " " " " "5-NNC.sub.6 H.sub.5 " " " " " "5-COOH.sub.3 " " " " " "5-COC.sub.6 H.sub.5 " " " " " "5-SO.sub.2 C.sub.6 H.sub.5 " " " " " "5-CO.sub.2 CH.sub.3 None CH.sub.3 " " " "" " H H " " "" 7-CH.sub.3 CH.sub.3 CH.sub.3 " " "" 7-NHCOCH.sub.3 H CH.sub.3 " " "" 7-OCH.sub.3 " " " " K.sup.+" 7-Cl " " " " "" 5-CH.sub.38-OCH.sub.3 " " " " "" 5-CH.sub.38-OC.sub.2 H.sub.5 " " " " "" 5,8-di-CH.sub.3 " " " " "" 8-OCH.sub.3 " " " " "" 5,8-di-OCH.sub.3 " " " " "" 7-NHCHO " " " " "" 7-NHCO.sub.2 C.sub.2 H.sub.5 " " " " "" 7-NHCOC.sub.6 H.sub.11 " " " " "" 7-CH.sub.3 " " " " H.sup.+" " " " " " NH.sub.4.sup.+4-CH.sub.35-CO.sub.2 CH.sub.3 " " " " " K.sup.+" " " " " " "" " " " 4-OCH.sub.3 " "" " " " 4-Br " "" " " " 2-Cl " "" " " " 4-CH.sub.3 " "" " " " 3-Cl " "" " " " 2,5-di-Cl " "" " " " 2,5-di-CH.sub.3 " "4-CH.sub.35-CO.sub.2 C.sub.2 H.sub.5 7-NHCOCH.sub.3 CH.sub.3 CH.sub.3 H " "" 7-OCH.sub.3 H CH.sub.3 " " "" H H H " " "" 7-CH.sub.3 CH.sub.3 CH.sub.3 " " "" " H CH.sub.3 " 2 "" " " " " 3 "" " " " " 4 "" " " " " 5 "" " " " " 6 "__________________________________________________________________________ TABLE 24______________________________________ ##STR69## Substituents onRing H (R.sub.1).sub.m R.sub.3 Z n M______________________________________None H H H 1 Na.sup.+4-CH.sub.3 7-CH.sub.3 " " " "4-C.sub.6 H.sub.5 " CH.sub.3 " " "4-CH.sub.3CN " " " " "4-C.sub.6 H.sub.5CHO " " " " "4-CH.sub.3SCN " " " " " ##STR70## " " " " "5-COC.sub.6 H.sub.5 " " " " "5-CHO " " " " "5-CN " " " " "5-COCH.sub.3 " " " " "5-SCN " " " " "5-NNC.sub.6 H.sub.5 " " " " "5-CONH.sub.2 " " " " "5-CONHC.sub.2 H.sub.4 OH " " " " "5-CON(C.sub.2 H.sub.5).sub.2 " " " " "5-SC.sub.4 H.sub.9n " " " " "5-SO.sub.2 C.sub.4 H.sub.9n " " " " "5-Br " " " " "5-SO.sub.2 C.sub.6 H.sub.5 " " " " "5-SO.sub.2 NH.sub.2 " " " " "5-SO.sub.2 NHC.sub.2 H.sub.5 " " " " "5-SO.sub.2 N(C.sub.2 H.sub.5).sub.2 " " " " " ##STR71## " " " " "5-CO.sub.2 C.sub.4 H.sub.9n " " " " "5-CO.sub.2 C.sub.2 H.sub.4 OCH.sub.3 " " " " "5-CO.sub.2 C.sub.2 H.sub.5 " " " " "4-CF.sub.3 " " " " "4-CH.sub.2 Cl " " " " "4-CF.sub.35-Br " " " " "5-SO.sub.3 C.sub.6 H.sub.5 " " " " "5-CO.sub.2 C.sub.6 H.sub.5 " " " " " ##STR72## 7-CH.sub.3 H " " NH.sub.4.sup.+" " H " " H.sup.+" " H " " K.sup.+" None CH.sub.3 " " "" 7-OCH.sub.3 " " " "" 7-Cl " " " "" 7-NHCOCH.sub.3 " " " "" 7-NHCHO " " " "" 7-NHSO.sub.2 CH.sub.3 " " " "" 7-NHCO.sub.2 CH.sub.3 " " " "" 7-NHCONHC.sub.2 H.sub.5 " " " " ##STR73## 7-CH.sub.3 " 4-CH.sub.3 " "" " " 3-CH.sub.3 " "" " " 2-CH.sub.3 " "" " " 2-Cl " "" " " 3-Cl " "" " " 2,5-di-Cl " "" " " 2,5-di-CH.sub.3 " "" " " 2-OCH.sub.3 " "" " " 4-OCH.sub.3 " "" " " H 2 "" " " " 3 "" " " " 4 "" " " " 5 "" " " " 6 "______________________________________

The invention has been described in detail with particular reference to preferred embodiments thereof, but it will be understood that variations and modifications can be effected within the spirit and scope of the invention.

Claims

1. A compound of the formula: ##STR74## wherein the thiophen-2-yl radical is unsubstituted or substituted with 1-3 groups selected from alkyl, cyano, alkoxycarbonyl, alkanoyl, alkylsulfonyl, arylsulfonyl, carbamoyl, alkylcarbamoyl, aryl, halogen, sulfamoyl, alkylsulfamoyl, and formyl; the coupler C is selected from ##STR75## wherein each R.sub.1 and Z is selected independently from alkyl, alkoxy, alkenyl of 2-6 carbons, halogen, alkanoylamino, and alkylthio; R.sub.2 is selected from hydrogen, alkyl, alkenyl of 2-6 carbons, aryl, cycloalkyl, and ##STR76## R.sub.3 and R.sub.4 are each selected from hydrogen and alkyl; M is H.sup.+, Na.sup.+, K.sup.+, or NH.sub.4.sup.+ ; n is 1-6; and m is 0, 1 or 2; and wherein all of the above defined alkyl, alkoxy, alkylene, alkenyl and cyclic moieties in the definitions of R.sub.1, R.sub.2 and Z are unsubstituted or substituted with 1-3 substituents selected from hydroxy, alkoxy, aryl, aryloxy, cyclohexyl, furyl, alkylcyclohexyl, aroyloxy, alkoxycarbonyl, alkanoyloxy, sulfamoyl, SO.sub.2 NH(aryl), SO.sub.2 NH(alkyl), SO.sub.2 N(dialkyl), NHCOO(alkyl), NHCONH(alkyl), alkanoylamino, alkylsulfonamido, succinimido, glutarimido, phthalimido, 2-pyrrolidono, cyano, carbamoyl, alkylcarbamoyl, alkoxyalkoxy, alkylthio, halogen, arylthio, alkylsulfonyl and arylsulfonyl.

2. A compound according to claim 1 wherein the thiophen-2-yl is as defined therein, and the coupler has the formula ##STR77## as defined therein.

3. A compound according to claim 1 wherein the thiophen-2-yl is as defined therein, and the coupler has the formula ##STR78## as defined therein.

4. A compound according to claim 1 wherein the thiophen-2-yl radical is substituted with 1-3 groups selected from alkyl, cyano, alkoxycarbonyl, alkanoyl, carbamoyl, alkylcarbamoyl, aryl, and formyl.

5. The compound according to claim 1 having the formula ##STR79##

6. The compound according to claim 1 having the formula ##STR80##

7. The compound according to claim 1 having the formula ##STR81##

8. The compound according to claim 1 having the formula ##STR82##

9. The compound according to claim 1 having the formula ##STR83##

10. The compound according to claim 1 having the formula ##STR84##