Bisazo dyes containing a 2-amino-substituted thiazole radical

Abstract

Compounds of the general formula I ##STR1## where D is the radical of a diazo component,R is hydrogen, hydroxy or unsubstituted or substituted alkyl, alkenyl, cycloalkyl, aralkyl, phenyl or heterocyclic ring,R.sup.1 and R.sup.2 independently of one another are hydrogen or unsubstituted or substituted alkyl, alkenyl, alkynyl, cycloalkyl, aralkyl or aryl, orR.sup.1 and R.sup.2 together with the nitrogen are a saturated heterocyclic 5-membered to 7-membered ring,X is hydrogen, chlorine, bromine, alkyl of 1 to 4 carbon atoms, alkoxy of 1 to 4 carbon atoms, allyloxy, .beta.-cyanoethoxy, benzyloxy, phenoxy, .beta.-alkoxycarbonylethoxy, where alkoxy is of 1 to 4 carbon atoms, alkylmercapto of 1 to 4 carbon atoms, phenylmercapto or alkanoylamino of 1 to 4 carbon atoms, andY is chlorine, alkyl of 1 to 4 carbon atoms, allyloxy, alkoxy of 1 to 4 carbon atoms or .beta.-cyanoethoxy, orX and Y together are a fused benzene ring which is unsubstituted or substituted by alkyl, alkoxy, chlorine or bromine.The compounds are in particular suitable for dyeing cotton and union fabrics of cotton and synthetic fibers, preferably polyesters. The dyeings obtained are, in part, very fast.

Description

BACKGROUND OF THE INVENTION

Summary of the Invention

The present invention relates to a compound of the general formula I ##STR2## where

D is the radical of a diazo component,

R is hydrogen, hydroxy or unsubstituted or substituted alkyl, alkenyl, cycloalkyl, aralkyl, phenyl or heterocyclic ring,

R.sup.1 and R.sup.2 independently of one another are hydrogen or unsubstituted or substituted alkyl, alkenyl, alkynyl, cycloalkyl, aralkyl or aryl, or

R.sup.1 and R.sup.2 together with the nitrogen are a saturated heterocyclic 5-membered to 7-membered ring, and

X is hydrogen, chlorine, bromine, alkyl of 1 to 4 carbon atoms, alkoxy of 1 to 4 carbon atoms, allyloxy, .beta.-cyanoethoxy, benzyloxy, phenoxy, .beta.-alkoxycarbonylethoxy, where alkoxy is of 1 to 4 carbon atoms, alkylmercapto of 1 to 4 carbon atoms, phenylmercapto or alkanoylamino of 1 to 4 carbon atoms and

Y is chlorine, alkyl of 1 to 4 carbon atoms, allyloxy, alkoxy of 1 to 4 carbon atoms or .beta.-cyanoethoxy, or

X and Y together are a fused benzene ring, the naphthalene nucleus formed being unsubstituted or substituted by alkyl, alkoxy, chlorine or bromine

DESCRIPTION OF THE PREFERRED EMBODIMENTS

Specific examples of radicals X and Y, in addition to those already mentioned in giving the general definition, are:

CH.sub.3, C.sub.2 H.sub.5, C.sub.3 H.sub.7, C.sub.4 H.sub.9, OCH.sub.3, OC.sub.2 H.sub.5, OC.sub.3 H.sub.7, OC.sub.4 H.sub.9, H.sub.3 COOCC.sub.2 H.sub.4 O, H.sub.5 C.sub.2 OOCC.sub.2 H.sub.4 O, H.sub.7 C.sub.3 OOCC.sub.2 H.sub.4 O, H.sub.9 C.sub.4 OOCC.sub.2 H.sub.4 O, H.sub.3 CCONH, H.sub.5 C.sub.2 CONH, CH.sub.3 S, H.sub.5 C.sub.2 S, H.sub.7 C.sub.3 S and H.sub.9 C.sub.4 S. Examples of radicals R, in addition to hydrogen and hydroxyl, are alkyl or alkenyl of 1 to 5 carbon atoms which is unsubstituted or substituted by hydroxyl, chlorine, cyano, alkoxy of 1 to 4 carbon atoms, alkanoyloxy of 1 to 4 carbon atoms, alkanoyl of 1 to 4 carbon atoms, alkoxycarbonyl (where alkoxy is of 1 to 4 carbon atoms), alkylmercapto of 1 to 4 carbon atoms, phenylmercapto, carbamoyl (which is unsubstituted or substituted) or sulfamoyl; cyclohexyl; phenylalkyl, where alkyl is of 1 to 5 carbon atoms; phenyl which is unsubstituted, or is monosubstituted or polysubstituted by chlorine, bromine, hydroxyl, alkoxy of 1 to 4 carbon atoms, alkyl of 1 to 4 carbon atoms, phenyl, phenoxy, alkylmercapto of 1 to 4 carbon atoms, phenylmercapto, alkanoylamino of 1 to 5 carbon atoms, .beta.-cyanoethoxy, .beta.-alkoxyethoxy (where alkoxy is of 1 to 4 carbon atoms), .beta.-alkoxycarbonylethoxy (where alkoxy is of 1 to 4 carbon atoms), .beta.-cyanoethylmercapto, .beta.-alkoxyethylmercapto (where alkoxy is of 1 to 4 carbon atoms) or .beta.-alkoxycarbonylethylmercapto (where alkoxy is of 1 to 4 carbon atoms); furyl, pyridyl or thienyl.

Specific examples of radicals R, in addition to those already mentioned, are:

C.sub.6 H.sub.3 (CH.sub.3).sub.2, C.sub.6 H.sub.4 CH.sub.3, C.sub.6 H.sub.4 C.sub.2 H.sub.5, C.sub.6 H.sub.4 Cl, C.sub.6 H.sub.3 Cl.sub.2, C.sub.6 H.sub.4 Br, C.sub.6 H.sub.3 Br.sub.2, C.sub.6 H.sub.4 F, C.sub.6 H.sub.3 F.sub.2, C.sub.6 H.sub.4 OCH.sub.3, C.sub.6 H.sub.4 OC.sub.2 H.sub.5, C.sub.6 H.sub.4 OC.sub.2 H.sub.4 CN, C.sub.6 H.sub.4 OC.sub.2 H.sub.4 COOCH.sub.3, C.sub.6 H.sub.4 OC.sub.2 H.sub.4 COOC.sub.2 H.sub.5, C.sub.6 H.sub.4 OC.sub.6 H.sub.5, C.sub.6 H.sub.4 NHCOCH.sub.3, C.sub.6 H.sub.4 NHCOC.sub.2 H.sub.5, C.sub.6 H.sub.4 NH.sub.2, C.sub.6 H.sub.4 NHCH.sub.3, ##STR3## C.sub.6 H.sub.4 SCH.sub.3, C.sub.6 H.sub.4 SC.sub.6 H.sub.5, CH.sub.3, C.sub.2 H.sub.5, ClCH.sub.2, C.sub.2 H.sub.5 OOC--CH.sub.2, CH.sub.3 OOC--CH.sub.2 and NC--CH.sub.2.

The radicals R.sup.1 and R.sup.2, which may be identical or different, are hydrogen or, for example, alkyl of 1 to 8 carbon atoms which is unsubstituted, alkyl of 2 to 8 carbon atoms which is substituted by hydroxyl, cyano, alkoxycarbonyl (where alkoxy is of 1 to 8 carbon atoms), alkoxy of 1 to 8 carbon atoms, phenoxy, phenoxyethoxy or benzyloxy, cyclohexyl, benzyl, phenylethyl, phenylhydroxyethyl, phenylpropyl, phenylbutyl, phenyl, which is unsubstituted or substituted by chlorine, methyl, methoxy or ethoxy, polyalkoxyalkyl, hydroxypolyalkoxyalkyl, alkanoyloxyalkyl or alkoxycarbonylalkyl of the type mentioned below.

Specific examples of radicals R.sup.1 and R.sup.2 are, amongst alkyl radicals, methyl, ethyl, propyl and butyl; amongst hydroxyalkyl radicals, .beta.-hydroxyethyl, .beta.-hydroxypropyl, .gamma.-hydroxypropyl and .omega.-hydroxyhexyl; .beta.-alkoxycarbonylethyl (where alkoxy is of 1 to 4 carbon atoms) and the radicals of the formulae ##STR4## and the acyloxyalkyl radicals of the formulae ##STR5## where acyl may be, for example, --COH, --COCH.sub.3, --COCH.sub.2 --O--C.sub.6 H.sub.5, or COOB or CONHB, where B is methyl or phenyl.

R.sup.1 and R.sup.2 may also be components of a heterocyclic ring, for example ##STR6##

The radical D of the diazo component is most frequently derived from the aniline, naphthalene, thiophen, aminoazobenzene, thiazole or benzthiazole series.

Examples of substituents of the radicals D of the diazo component are:

In the benzene series: chlorine, bromine, nitro, cyano, trifluoromethyl, methylsulfonyl, ethylsulfonyl, phenylsulfonyl, carbomethoxy, carbobutoxy, carbo-.beta.-methoxyethoxy, carboxamide and sulfonamide, which are unsubstituted or N-monosubstituted or N-disubstituted, methyl, ethyl, methoxy and ethoxy. In this context, examples of N-substituents of carboxamide or sulfonamide groups are methyl, ethyl, propyl, butyl, .beta.-ethylhexyl, .beta.-methoxyethyl, .gamma.-methoxypropyl and .gamma.-ethoxypropyl; the amide portion of a substituted carboxamide or sulfonamide may also be pyrrolidide, piperidide or morpholide.

In the azobenzene series: chlorine, bromine, nitro, cyano, methyl, hydroxyl, ethyl, methoxy and ethoxy.

In the heterocyclic series: chlorine, bromine, nitro, cyano, methyl, ethyl, phenyl, methoxy, ethoxy, carbomethoxy, carboethoxy, acetyl, methylsulfonyl and ethylsulfonyl.

Specific examples of amines from which the radical D may be derived are: aniline, o-, m- and p-toluidine, o-, m- and p-nitroaniline, o-, m- and p-cyanoaniline, 2,4-dicyanoaniline, o-, m- and p-chloroaniline, o-, m- and p-bromoaniline, 2,4,6-tribromoaniline, 2-chloro-4-nitroaniline, 2-bromo-4-nitroaniline, 2-cyano-4-nitroaniline, 2-methylsulfonyl-4-nitroaniline, 2-methyl-4-nitroaniline, 2-methoxy-4-nitroaniline, 4-chloro-2-nitroaniline, 4-methyl-2-nitroaniline, 4-methoxy-2-nitroaniline, 1-amino-2-trifluoromethyl-4-chlorobenzene, 2-chloro-5-aminobenzonitrile, 2-amino-5-chlorobenzonitrile, 1-amino-2-nitrobenzene-4-sulfonic acid n-butylamide and .beta.-methoxyethylamide, 2,4-dinitroaniline, 2,4-dinitro-6-chloroaniline, 2,4-dinitro-6-bromoaniline, 2,4-dinitro-6-cyanoaniline, 1-amino-2,4-dinitrobenzene-6-methylsulfone, 2,6-dichloro-4-nitroaniline, 2,6-dibromo-4-nitroaniline, 2-chloro-6-bromo-4-nitroaniline, 2,6-dicyano-4-nitroaniline, 2-cyano-4-nitro-6-chloroaniline, 2-cyano-4-nitro-6-bromoaniline, 1-aminobenzene-4-methylsulfone, 1-amino-2,6-dibromo-benzene-4-methylsulfone, 1-amino-2,6-dichlorobenzene-4-methylsulfone, 1-amino-2,4-dinitrobenzene-6-carboxylic acid methyl ester and .beta.-methoxyethyl ester, propyl 3,5-dichloroanthranilate, .beta.-methoxyethyl 3,5-dibromoanthranilate, N-acetyl-p-phenylenediamine, 4-aminoacetophenone, 4- and 2-amino-benzophenone, 2- and 4-aminodiphenylsulfone, methyl, ethyl, propyl, butyl, isobutyl, .beta.-methoxyethyl and .beta.-ethoxyethyl 2-aminobenzoate, 3-aminobenzoate and 4-aminobenzoate, methyl, isobutyl, .beta.-methoxyethyl and .beta.-butoxyethyl 5-nitro-anthranilate, 3- and 4-aminobenzoic acid amide, methylamide, propylamide, butylamide, isobutylamide, cyclohexylamide, .beta.-ethyl-hexylamide, .gamma.-methoxypropylamide and .gamma.-ethoxypropylamide, 2-, 3- and 4-aminobenzoic acid dimethylamide, diethylamide, pyrrolidide and morpholide, 2-, 3- and 4-aminobenzenesulfonic acid dimethylamide and diethylamide and 2-aminobenzthiazole.

Examples of suitable diazo components of the aminoazobenzene series are: 4-aminoazobenzene, 2',3-dimethyl-4-aminoazobenzene, 3',2-dimethyl-4-aminoazobenzene, 2,5-dimethyl-4-aminoazobenzene, 2-methyl-5-methoxy-4-aminoazobenzene, 2-methyl-4',5-dimethoxy-4-aminoazobenzene, 2,5-dimethoxy-4-aminoazobenzene, 4'-methoxy-2,5-dimethyl-4-aminoazobenzene and 3-methoxy-4-aminoazobenzene.

The diazo components preferably have, for example, the following formulae: ##STR7##

A compound of the formula I may be prepared by reacting a diazonium compound of an amine of the formula ##STR8## with a coupling component of the formula II ##STR9## D, X, Y, R, R.sup.1 and R.sup.2 having the meanings given above.

Details of the method of preparation may be found in the Examples, where parts and percentages are by weight, unless stated otherwise.

Compounds of the formula II may be prepared by a method similar to that described in French Pat. No. 1,600,940.

In particular, the invention provides compounds of the formula I, where

D is phenyl which is substituted by fluorine, chlorine, bromine, nitro, phenylazo, cyano, alkyl of 1 to 5 carbon atoms, alkoxy of 1 to 4 carbon atoms, alkoxycarbonyl (where alkoxy is of 1 to 8 carbon atoms), alkylsulfonyl of 1 to 4 carbon atoms, ##STR10## or trifluoromethyl, or is thiazolyl which is unsubstituted or substituted by methyl, nitro, alkanoyl of 1 to 4 carbon atoms, alkoxycarbonyl (where alkoxy is of 1 to 5 carbon atoms), cyano, carbamoyl or phenyl, or is benzthiazolyl which is unsubstituted or substituted by chlorine, bromine, alkoxy of 1 to 4 carbon atoms, nitro, alkoxycarbonyl (where alkoxy is of 1 to 4 carbon atoms) or methyl-sulfonyl or is 1,2-benzisothiazolyl or 2,1-benzisothiazolyl, which are unsubstituted or substituted by chlorine, bromine, nitro or cyano, R is phenyl which is unsubstituted or is monosubstituted or polysubstituted by chlorine, bromine, hydroxyl, alkoxy of 1 to 4 carbon atoms, phenoxy, alkyl of 1 to 10 carbon atoms, phenyl, alkylmercapto of 1 to 4 carbon atoms, phenylmercapto, alkanoylamino of 1 to 8 carbon atoms, .beta.-cyanoethoxy, .beta.-alkoxyethoxy (where alkoxy is of 1 to 4 carbon atoms), .beta.-alkoxycarbonylethoxy (where alkoxy is of 1 to 4 carbon atoms), .beta.-cyanoethylmercapto, .beta. -alkoxyethylmercapto (where alkoxy is of 1 to 4 carbon atoms) or .beta.-alkoxycarbonylethylmercapto (where alkoxy is of 1 to 4 carbon atoms), or is naphthyl, pyridyl, furyl or thienyl.

R.sup.1 and R.sup.2 independently of one another are hydrogen or allyl or are alkyl of 1 to 8 carbon atoms which is unsubstituted or substituted by cyano, alkoxycarbonyl (where alkoxy is of 1 to 8 carbon atoms), (OCH.sub.2 CH.sub.2).sub.n OT, ##STR11## or phenyl, or are cyclohexyl or phenylhydroxyethyl, or are phenyl which is unsubstituted or substituted by chlorine, methyl, methoxy or ethoxy, or

R.sup.1 and R.sup.2 together with the nitrogen are pyrrolidino, piperidino, morpholino, hexamethyleneimino or N-methylpiperazino,

n is 0, 1 or 2,

T is hydrogen, alkyl of 1 to 8 carbon atoms, cyclohexyl, benzyl, phenylethyl, phenyl, tolyl or alkanoyl of 1 to 8 carbon atoms, and

X is hydrogen, chlorine, bromine, alkyl of 1 to 4 carbon atoms, alkoxy of 1 to 4 carbon atoms, allyloxy, .beta.-cyanoethoxy, benzyloxy, phenoxy, .beta.-alkoxycarbonylethoxy (where alkoxy is of 1 to 4 carbon atoms), alkylmercapto of 1 to 4 carbon atoms, phenylmercapto or alkanoylamino of 1 to 4 carbon atoms, and

Y is chlorine, alkyl of 1 to 4 carbon atoms, allyloxy, alkoxy of 1 to 4 carbon atoms or .beta.-cyanoethoxy, or

X and Y together are a fused benzene ring, the naphthalene nucleus formed being unsubstituted or substituted by alkyl of 1 to 4 carbon atoms, chlorine or bromine.

Compounds of particular industrial importance are those of the formula Ia ##STR12## where

B is

C.sub.6 H.sub.5, C.sub.6 H.sub.4 CH.sub.3, C.sub.6 H.sub.4 C.sub.2 H.sub.5, C.sub.6 H.sub.4 Cl, C.sub.6 H.sub.3 Cl.sub.2, C.sub.6 H.sub.4 OCH.sub.3, C.sub.6 H.sub.4 OC.sub.2 H.sub.4 CN, C.sub.5 H.sub.4 NHCOCH.sub.3 or C.sub.6 H.sub.4 NH.sub.2,

B.sup.1 and B.sup.2 independently of one another are

CH.sub.3, C.sub.2 H.sub.5, C.sub.3 H.sub.7, C.sub.4 H.sub.9, C.sub.2 H.sub.4 COOCH.sub.3, C.sub.2 H.sub.4 COOC.sub.2 H.sub.5, C.sub.2 H.sub.4 CN, C.sub.2 H.sub.4 OH, C.sub.2 H.sub.4 C.sub.6 H.sub.5, C.sub.2 H.sub.4 OCOCH.sub.3, C.sub.2 H.sub.4 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5, C.sub.2 H.sub.4 OCH.sub.3, C.sub.3 H.sub.6 OCH.sub.3, C.sub.6 H.sub.5, C.sub.6 H.sub.4 Cl, benzyl or CH.sub.2 CH.dbd.CH.sub.2,

X.sup.1 is OCH.sub.3, OC.sub.2 H.sub.5, OC.sub.4 H.sub.9, OC.sub.2 H.sub.4 CN, OC.sub.2 H.sub.4 COOCH.sub.3, CH.sub.3, C.sub.2 H.sub.5, SCH.sub.3, NHCOCH.sub.3 or NHCOC.sub.2 H.sub.5 and

Y.sup.1 is OCH.sub.3, OC.sub.2 H.sub.5, OC.sub.4 H.sub.9, OC.sub.2 H.sub.4 CN, CH.sub.3 or C.sub.2 H.sub.5 and X.sup.1 and Y.sup.1 may be identical or different,

Z.sup.1 is hydrogen, chlorine, bromine, cyano or nitro,

Z.sup.2 is hydrogen, chlorine, bromine or nitro and

Z.sup.3 is hydrogen, chlorine, bromine, cyano or alkoxycarbonyl (where alkoxy is of 1 to 4 carbon atoms).

The dyes of the formula I are preferentially usable for dyeing and, in particular, printing cotton and union fabrics containing cotton, the other component preferably being a polyester. Suitable dyeing and printing processes are those described in German Pat. No. 1,811,796. The dyes of the invention, which have a high tinctorial strength, give lightfast and wetfast dyeings and prints which also have good fastness to crocking.

EXAMPLE 1

17.2 parts of 2-chloro-4-nitroaniline are diazotized in the conventional manner. A solution of 15.3 parts of 1-amino-2,5-dimethoxybenzene in 300 parts of water and 25 parts of 5-normal hydrochloric acid is run into the filtered nitrite-free diazonium salt solution, whilst stirring. As coupling proceeds, the reaction mixture becomes viscous; it is therefore diluted with about 1,000 parts of water. After completion of coupling, the dye is filtered off and washed neutral with water. The paste of the monoazo dye is stirred into a mixture of 600 parts of acetic acid and 12 parts of concentrated hydrochloric acid at from 50.degree. to 60.degree. C. The temperature is then lowered to 20.degree.-25.degree. C. by external cooling and a solution of 9.0 parts of sodium nitrite is added over from 5 to 10 minutes. After about 60 minutes, the excess nitrite is removed with amidosulfonic acid. A solution of 25.6 parts of 4-phenyl-2-(N-diallylamino)-thiazole in 40 parts of acetic acid is added to the filtered diazonium salt solution over 30 minutes. The pH is then raised to 2.5 with aqueous sodium acetate solution. After completion of coupling, the disazo dye is filtered off, washed first with isopropanol and then with hot water, and dried. The dye which has the following formula ##STR13## is very suitable for printing cotton or cotton/polyester union fabrics. Navy to black dyeings are obtained.

The dyes summarized in the Table which follows can be prepared by a method similar to that described in Example 1 and give dyeings having similar properties.

__________________________________________________________________________ ##STR14##Ex-ample D X.sup.1 Y.sup.1 B B.sup.1 B.sup.2 Hue__________________________________________________________________________ ##STR15## OCH.sub.3 OCH.sub.3 ##STR16## CH.sub.2 CHCH.sub.2 CH.sub.2 CHCH.sub.2 navy3 " " " ##STR17## " " "4 " " " ##STR18## " " "5 " " " C.sub.6 H.sub.5 C.sub.2 H.sub.5 C.sub.2 H.sub.5 "6 " " " ##STR19## CH.sub.2 CHCH.sub.2 CH.sub.2 CHCH.sub.2 "7 ##STR20## " " ##STR21## " " "8 " " " ##STR22## " " "9 " " " ##STR23## " " "10 " " " ##STR24## " " "11 ##STR25## " " C.sub.6 H.sub.5 C.sub.2 H.sub.5 C.sub.2 H.sub.5 "12 " " " ##STR26## CH.sub.3 CH.sub.3 "13 ##STR27## " " C.sub.6 H.sub.5 CH.sub.2 CHCH.sub.2 CH.sub.2 CHCH.sub.2 reddish blue14 " " " ##STR28## " " reddish blue15 " " " " C.sub.2 H.sub.5 C.sub.2 H.sub.5 reddish blue16 " " " ##STR29## CH.sub.3 CH.sub.3 reddish blue17 " " " ##STR30## " " reddish blue18 ##STR31## " " C.sub.6 H.sub.5 C.sub.2 H.sub.5 C.sub.2 H.sub.5 violet19 ##STR32## CH.sub.3 CH.sub.3 ##STR33## CH.sub.2 CHCH.sub.2 CH.sub.2 CHCH.sub.2 "20 ##STR34## OCH.sub.3 OCH.sub.3 ##STR35## " " "21 " " " ##STR36## C.sub.2 H.sub.5 C.sub.2 H.sub.5 "22 " " " ##STR37## " " "__________________________________________________________________________

EXAMPLE 23

20.7 parts of 2,6-dichloro-4-nitroaniline are introduced into a mixture of 40 parts of concentrated sulfuric acid and 30 parts of nitrosylsulfuric acid (of from 40 to 45% strength) at 10.degree.-15.degree. C., whilst stirring, and the diazotization is allowed to take place overnight at room temperature. The solution is then poured onto a mixture of 200 parts of ice and 200 parts of water. After having removed excess nitrite, a solution of 15.3 parts of 1-amino-2,5-dimethoxybenzene in 300 parts of water and 25 parts of 5-normal hydrochloric acid is added over about 30 minutes. As coupling proceeds, the reaction mixture becomes viscous; it is therefore diluted with about 700 parts of water. After completion of coupling, the dye is filtered off and washed neutral with water. The filter cake of the monoazo dye is dissolved in 400 parts of acetic acid by stirring at room temperature and after adding 12 parts of concentrated hydrochloric acid the dye is diazotized with an aqueous solution of 8.0 parts of sodium nitrite. After about 3 hours at 20.degree.-25.degree. C. the diazotization is complete, and a solution of 25.6 parts of 4-phenyl-2-(N-diallylamino)-thiazole in 40 parts of acetic acid is added to the nitrite-free diazonium salt solution. Coupling is then completed by means of an aqueous solution of 10 parts of sodium acetate, at pH 3-4. The dye is filtered off and washed first with isopropanol and then with hot water. After drying under reduced pressure at 60.degree. C., 46 parts of a dark powder having the following formula ##STR38## are obtained. This product is very suitable for printing cotton or cotton/polyester union fabrics. Navy to black dyeings are obtained.

The dyes summarized in the Table which follows can be prepared by a method similar to that described in Example 23 and give dyeings having similar properties.

__________________________________________________________________________ ##STR39##Ex-ample D X.sup.1 Y.sup.1 B B.sup.1 B.sup.2 Hue__________________________________________________________________________24 ##STR40## OCH.sub.3 OCH.sub.3 C.sub.6 H.sub.5 C.sub.2 H.sub.5 C.sub.2 H.sub.5 black25 " " " " " C.sub.6 H.sub.5 "26 " " " ##STR41## CH.sub.2 CHCH.sub.2 CH.sub.2 CHCH.sub.2 "27 ##STR42## " " C.sub.6 H.sub.5 C.sub.2 H.sub.5 C.sub.2 H.sub.4 COOC.sub.2 H.sub.5 "28 ##STR43## " " ##STR44## CH.sub.2 CHCH.sub.2 CH.sub.2 CHCH.sub.2 "29 " " " ##STR45## " " "30 ##STR46## " CH.sub.3 C.sub.6 H.sub.5 " " navy31 " " " " C.sub.2 H.sub.5 C.sub.2 H.sub.5 "32 " " " " " C.sub.2 H.sub.4 COOC.sub.2 H.sub.5 "33 " " " ##STR47## CH.sub.2 CHCH.sub.2 CH.sub.2 CHCH.sub.2 "34 " " OCH.sub.3 C.sub.6 H.sub.5 C.sub.6 H.sub.5 C.sub.2 H.sub.4 OH "35 " " " ##STR48## C.sub.2 H.sub.5 C.sub.2 H.sub.5 black36 " " CH.sub.3 ##STR49## C.sub.2 H.sub.5 C.sub.2 H.sub.4 OCOOC.sub.2 H.sub.5 "37 " " " ##STR50## CH.sub.3 CH.sub.3 "38 " " " ##STR51## CH.sub.2 CHCH.sub.2 CH.sub.2 CHCH.sub.2 navy39 " " " ##STR52## " " violet40 ##STR53## CH.sub.3 CH.sub.3 ##STR54## " " black41 ##STR55## OCH.sub.3 OCH.sub.3 C.sub.6 H.sub.5 " " "42 " " " " C.sub.2 H.sub.5 C.sub.2 H.sub.5 "43 " " " " " C.sub.2 H.sub.4 COOCH.sub.3 . "44 ##STR56## " " " " C.sub.2 H.sub.5 "45 ##STR57## " " " CH.sub.2 CHCH.sub.2 CH.sub.2 CHCH.sub.2 blue46 " " " " " " "47 " " " ##STR58## " " "48 ##STR59## CH.sub.3 CH.sub.3 C.sub.6 H.sub.5 C.sub.2 H.sub.5 C.sub.2 H.sub.5 "49 ##STR60## " " " " " "50 ##STR61## OCH.sub.3 OCH.sub.3 " " " violet51 " " " " " C.sub.2 H.sub.4 CN "52 " " " " " C.sub.2 H.sub.4 OCOCH.sub.3 "53 ##STR62## " " " C.sub.2 H.sub.4 OCOCH.sub.3 " navy54 ##STR63## " CH.sub.3 ##STR64## C.sub.2 H.sub.5 C.sub.2 H.sub.4 COOC.sub.2 H.sub.5 blue55 ##STR65## " " ##STR66## " C.sub.2 H.sub.5 "56 ##STR67## " " " " " "57 ##STR68## " " " " " "58 ##STR69## " " " " " "59 ##STR70## " OCH.sub.3 C.sub.6 H.sub.5 CH.sub.2 CHCH.sub.2 C.sub.2 H.sub.4 COOC.sub.2 H.sub.5 black60 ##STR71## " CH.sub.3 ##STR72## C.sub.2 H.sub.5 C.sub.3 H.sub.7 "61 ##STR73## " OCH.sub.3 C.sub.6 H.sub.5 C.sub.4 H.sub.9 C.sub.4 H.sub.9 "62 " " CH.sub.3 ##STR74## " " "63 " " " ##STR75## C.sub.3 H.sub.7 C.sub.2 H.sub.4 COOOC.sub.2 H.sub.5 "64 " " " " CH.sub.3 ##STR76## "65 ##STR77## " " ##STR78## C.sub.2 H.sub.5 " blue66 ##STR79## " " " " C.sub.2 H.sub.5 green- ish blue67 " " " ##STR80## CH.sub.2 CHCH.sub.2 CH.sub.2 CHCH.sub.2 green- ish blue68 ##STR81## " " C.sub.6 H.sub.5 " " blue__________________________________________________________________________

EXAMPLE 69

13.8 parts of p-nitroaniline are diazotized in the conventional manner. A solution of 15 parts of .alpha.-naphthylamine in 50 parts of acetic acid is allowed to run into the filtered nitrite-free diazonium salt solution, whilst stirring. As coupling proceeds, the reaction mixture becomes viscous. It is therefore diluted with about 400 parts of water. After completion of coupling, the pH is brought to 6-7 with 30% strength aqueous sodium hydroxide solution. The dye is filtered off and washed thoroughly with water. The paste of the monoazo dye is stirred thoroughly into a mixture of 800 parts of acetic acid and 12 parts of concentrated hydrochloric acid at 50.degree.-60.degree. C. The temperature is then lowered to 0.degree.-10.degree. C. by external cooling and a solution of 8.3 parts of sodium nitrite is added over 5-10 minutes. After about 30 minutes, the excess nitrite is removed with amidosulfonic acid. A solution of 26.6 parts of 2-(n-.beta.-methoxycarbonylethyl-N-ethyl)-4-phenylthiazole in 60 parts of acetic acid is added to the filtered diazonium salt solution over 30 minutes. The pH is then raised to 2.5 with aqueous sodium acetate solution. After completion of coupling, the disazo dye is filtered off, washed first with isopropanol and then with hot water, and dried. The dye, which has the following structure ##STR82## is very suitable for dyeing or printing cotton or cotton/polyester union fabrics. Navy to black dyeings are obtained.

The dyes summarized in the Table which follows can be prepared by a method similar to that described in Example 1 and give dyeings having similar properties.

______________________________________ ##STR83##Ex-ample R R.sup.1 R.sup.2______________________________________70 C.sub.6 H.sub.5 CH.sub.3 ##STR84##71 " C.sub.2 H.sub.4 OH CH.sub.372 " " C.sub.2 H.sub.573 " CH.sub.3 ##STR85##74 " C.sub.2 H.sub.5 "75 " CH.sub.2 CHCH.sub.2 CH.sub.2 CHCH.sub.276 " ##STR86## ##STR87##77 " C.sub.2 H.sub.5 C.sub.2 H.sub.578 " " C.sub.2 H.sub.4 CN79 " CH.sub.3 C.sub.6 H.sub.580 " ##STR88##81 " ##STR89##82 " ##STR90##83 ##STR91## CH.sub.2 CHCH.sub.2 CH.sub.2 CHCH.sub.284 ##STR92## C.sub.3 H.sub.7 C.sub.3 H.sub.785 ##STR93## CH.sub.2 CHCH.sub.2 CH.sub.2 CHCH.sub.286 ##STR94## " "87 " C.sub.2 H.sub.5 C.sub.2 H.sub.588 " " ##STR95##89 " C.sub.3 H.sub.7 C.sub.3 H.sub.790 ##STR96## CH.sub.2 CHCH.sub.2 C.sub. 2 H.sub.4 COCH.sub.391 ##STR97## C.sub.2 H.sub.5 C.sub.2 H.sub.592 ##STR98## " ##STR99##93 ##STR100## H ##STR101##94 ##STR102## C.sub.2 H.sub.5 C.sub.2 H.sub.4 CN95 H " C.sub.2 H.sub.596 CH.sub.3 " ##STR103##97 " CH.sub.2 CHCH.sub.2 "98 ##STR104## C.sub.2 H.sub.5 C.sub.2 H.sub.599 ##STR105## " "100 ##STR106## CH.sub.2 CHCH.sub.2 CH.sub.2 CHCH.sub.2101 HO " C.sub.2 H.sub.5______________________________________ __________________________________________________________________________ ##STR107##Example D R R.sup.1 R.sup.2__________________________________________________________________________102 ##STR108## C.sub.6 H.sub.5 C.sub.2 H.sub.5 ##STR109##103 " ##STR110## " "104 " ##STR111## " "105 ##STR112## ##STR113## " C.sub.2 H.sub.5106 C.sub.6 H.sub.5 " CH.sub.2 CHCH.sub.2 CH.sub.2 CHCH.sub.2107 ##STR114## C.sub.6 H.sub.5 C.sub.2 H.sub.5 C.sub.2 H.sub.4OCOCH.sub.3108 ##STR115## " " "109 " " " C.sub.2 H.sub.5110 ##STR116## " " "111 ##STR117## ##STR118## CH.sub.2 CHCH.sub.2 CH.sub.2 CHCH.sub.2112 " ##STR119## C.sub.2 H.sub.5 C.sub.2 H.sub.5113 ##STR120## ##STR121## " "114 " ##STR122## " "115 " ##STR123## CH.sub.2 CHCH.sub.2 CH.sub.2 CHCH.sub.2116 ##STR124## C.sub.6 H.sub.5 C.sub.2 H.sub.5 C.sub.2 H.sub.5117 ##STR125## ##STR126## CH.sub.2 CHCH.sub.2 CH.sub.2 CHCH.sub.2118 ##STR127## C.sub.6 H.sub.5 CH.sub.2 CHCH.sub.2 ##STR128##119 " ##STR129## C.sub.2 H.sub.5 "120 " C.sub.6 H.sub.5 " C.sub.2 H.sub.4 CN121 ##STR130## " " ##STR131##122 ##STR132## " " ##STR133##123 " ##STR134## " "125 " C.sub.6 H.sub.5 CH.sub.2 CHCH.sub.2 "126 " ##STR135## C.sub.2 H.sub.5 C.sub.2 H.sub.5127 " C.sub.6 H.sub.5 C.sub.2 H.sub.5 ##STR136##128 " ##STR137## " ##STR138##129 ##STR139## C.sub.6 H.sub.5 " ##STR140##130 ##STR141## C.sub.6 H.sub.5 CH.sub.2 CHCH.sub.2 ##STR142##131 " ##STR143## " "132 ##STR144## ##STR145## C.sub.2 H.sub.5 C.sub.2 H.sub.5133 ##STR146## C.sub.6 H.sub.5 CH.sub.2 CHCH.sub.2 CH.sub.2 CHCH.sub.2134 " " C.sub.3 H.sub.7 C.sub.3 H.sub.7__________________________________________________________________________

EXAMPLE 135

18.3 parts of 2,4-dinitroaniline are introduced into a mixture of 29 parts of nitrosylsulfuric acid (containing 13.1% of dinitrogen trioxide) and 120 parts of 85% strength sulfuric acid at 0.degree.-5.degree. C., whilst stirring. After about 4 hours at 0.degree.-5.degree. C., the diazotization is complete and the solution is added dropwise, whilst stirring, to a solution of 15 parts of .alpha.-naphthylamine, 400 ml of water and 15 parts of concentrated hydrochloric acid, which is cooled to 0.degree. C. by adding 400 parts of ice. Coupling is complete after 2-3 hours. The reaction mixture is neutralized with dilute sodium hydroxide solution, the product is filtered off and washed salt-free with water, and thereafter the procedure is continued as in Example 69. The resulting disazo dye, having the following composition ##STR147## dyes cotton, and cotton/polyester union fabrics, in lightfast greenish blue hues.

The dyes summarized in the Table which follows can be prepared by a method similar to that described in Example 135 and give dyeings having similar properties.

__________________________________________________________________________ ##STR148##Example D R R.sup.1 R.sup.2__________________________________________________________________________136 ##STR149## C.sub.6 H.sub.5 C.sub.2 H.sub.5 C.sub.2 H.sub.5137 " " ##STR150## ##STR151##138 " " CH.sub.2 CHCH.sub.2 CH.sub.2 CHCH.sub.2139 " ##STR152## " "140 " ##STR153## " "141 " ##STR154## C.sub.2 H.sub.5 C.sub.2 H.sub.5142 " C.sub. 6 H.sub.5 " C.sub.2 H.sub.4 CN143 " ##STR155## " "144 " H " C.sub.2 H.sub.5145 " CH.sub.3 CH.sub.2 CHCH.sub.2 ##STR156##146 " ##STR157## C.sub.2 H.sub.5 C.sub.2 H.sub.5147 " ##STR158## " "148 " ##STR159## " "149 " HO " "150 " CH.sub.3 H ##STR160##151 ##STR161## C.sub.6 H.sub.5 C.sub.2 H.sub.5 C.sub.2 H.sub.5152 " ##STR162## " "153 ##STR163## C.sub.6 H.sub.5 C.sub.6 H.sub.5 "154 " " CH.sub.2 CHCH.sub.2 CH.sub.2 CHCH.sub.2155 ##STR164## " C.sub.2 H.sub.5 C.sub.2 H.sub.5156 ##STR165## " " "157 ##STR166## " C.sub.2 H.sub.5 ##STR167##158 " " " C.sub.2 H.sub.5159 ##STR168## ##STR169## " "160 " " " ##STR170##161 ##STR171## C.sub.6 H.sub.5 C.sub.2 H.sub.5 C.sub.2 H.sub.5162 ##STR172## " " "163 ##STR173## " " "164 ##STR174## " " "165 " ##STR175## " "166 " ##STR176## C.sub.2 H.sub.5 C.sub.2 H.sub.4 CN167 " ##STR177## " C.sub.2 H.sub.5168 " CH.sub.3 CH.sub.2 CHCH.sub.2 CH.sub.2 CHCH.sub.2169 " C.sub.2 H.sub.5 C.sub.2 H.sub.5170 ##STR178## " " "171 ##STR179## " CH.sub.2 CHCH.sub.2 ##STR180##172 ##STR181## ##STR182## " "173 ##STR183## " " "174 ##STR184## C.sub.6 H.sub.5 C.sub.2 H.sub.5 C.sub.2 H.sub.5175 ##STR185## " " "176 ##STR186## " " "177 ##STR187## " " ##STR188##178 ##STR189## " C.sub.3 H.sub.7 "179 ##STR190## " C.sub.2 H.sub.5 C.sub.2 H.sub.5180 ##STR191## ##STR192## " "181 ##STR193## " " ##STR194##182 ##STR195## C.sub.6 H.sub.5 " "183 ##STR196## " " ##STR197##184 " " CH.sub.2 CHCH.sub.2 "185 " " C.sub.2 H.sub.5 C.sub.2 H.sub.5186 ##STR198## " " "187 ##STR199## " CH.sub.2 CHCH.sub.2 CH.sub.2 CHCH.sub.2188 ##STR200## " " "189 ##STR201## " " "190 ##STR202## " "__________________________________________________________________________

Claims

1. A compound of the formula: ##STR203##

2. A compound of the formula: ##STR204##