TREA

Water-soluble azo dyes containing diaminopyrimidine coupler components

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Information

  • Patent Grant
  • 4145341
  • Patent Number
    4,145,341
  • Date Filed
    Monday, December 22, 1975
    49 years ago
  • Date Issued
    Tuesday, March 20, 1979
    45 years ago
Information
Abstract
Dyes having the formula: ##STR1## IN WHICH D is the radical of a diazo component; andA is the radical of a pyrimidine coupling component bearing two unsubstituted or substituted amino groups as substituents. The dyes are eminently suitable for dyeing natural and synthetic polyamides; brilliant colorations are obtained.
Description

The invention relates to dyes which in the form of the free acid correspond to the formula (I): ##STR2## in which
D is the radical of a diazo component; n is one of the integers 1, 2 and 3; A is a radical of the formula (IIa) or (IIb): ##STR3##
Z is hydrogen or unsubstituted or substituted alkyl, cycloalkyl, aralkyl or aryl; and
Z.sup.1, Z.sup.2, Z.sup.3 and Z.sup.4 independently of one another may be hydrogen or unsubstituted or substituted alkyl, cycloalkyl, polycycloalkyl, aralkyl or aryl.
One of the radicals Z.sup.1 to Z.sup.4 is preferably other than hydrogen.
The invention relates particularly to dyes of the formula (III): ##STR4## in which
D and n have the above meanings and
A.sup.1 is a radical of the formula (IVa) of (IVb): ##STR5##
B is hydrogen, alkyl, alkyl bearing hydroxy, alkoxy, alkanoyloxy or phenoxy as a substituent, aralkyl, cycloalkyl, phenyl or phenyl bearing alkyl, halogen, nitro, cyano, alkoxycarbonyl, carbamoyl or sulfamoyl as a substituent;
R is hydrogen, alkyl of one to eight carbon atoms which may be interrupted by oxygen atoms and which may bear hydroxy, acyloxy, alkoxy, cyano, cycloalkoxy, aralkoxy or aroxy as a substituent, cycloalkyl or polycycloalkyl of five to fifteen carbon atoms which may bear hydroxy, chloro, hydroxyalkyl, chloroalkyl or alkyl as a substituent, aralkyl of seven to fifteen carbon atoms, phenyl, phenyl bearing chloro, hydroxy, alkoxy, alkyl, hydroxyalkyl or hydroxyalkoxy as a substituent, alkenyl, pyrrolidonylalkyl or carboxyalkyl;
R.sup.1 is hydrogen, alkyl of one to eight carbon atoms or hydroxyalkyl of two to nine carbon atoms;
R and R.sup.1 with the nitrogen may be the radical of pyrrolidine, piperidine or morpholine; and, independently of each other,
R.sup.2 may have the same meaning as R;
R.sup.3 may have the same meaning as R.sup.1 ; and
R.sup.2 and R.sup.3 together may have the same meaning as R and R.sup.1 together;
and in which the radical D and/or the substituents B and R to R.sup.3 may contain sulfonic acid groups.
The radical D of the diazo component may be derived particularly from aniline, aminophthalimide and aminoazobenzene derivatives and these may bear for example hydroxysulfonyl, halogen, hydroxy, alkyl, alkoxy, acylamino, cyano, alkylsulfone, phenylsulfone, nitro, carboxyl, carbalkoxy, carbamoyl, N-substituted carbamoyl, sulfamoyl, N-substituted sulfamoyl or benzothiazolyl.
Examples of individual substituents, in addition to those already mentioned, are: chloro, bromo, methyl, ethyl, trifluoromethyl, methoxy, ethoxy, methylsulfonyl, ethylsulfonyl, carbomethoxy, carboethoxy, carbo-.beta.-ethoxyethoxy, carbo-.beta.-methoxyethoxy, carbobutoxy, carbo-.beta.-butoxyethoxy, N-methylcarbamoyl, N-ethylcarbamoyl, N-butylcarbamoyl, N-hexylcarbamoyl, N-.beta.-ethylhexylcarbamoyl, N-.beta.-hydroxyethylcarbamoyl, N-.beta.-methoxyethylcarbamoyl, N-.gamma.-methoxypropylcarbamoyl, N,N-dimethylcarbamoyl, N,N-diethylcarbamoyl, N-methyl-N-.beta.-hydroxyethylcarbamoyl, N-phenylcarbamoyl, carboxylic acid piperidide, morpholide or pyrrolidide and the corresponding sulfonamides, acetylamino, propionylamino, butyrylamino, methylsulfonylamino, phenylsulfonylamino, hydroxyacetylamino, benzoylamino, p-chlorobenzoylamino, phenylacetylamino and the radicals of the formulae ##STR6##
Examples of radicals Z or B (other than hydrogen) are: alkyl of one to seven carbon atoms, methoxyethyl, ethoxyethyl, phenoxyethyl, benzyl, phenylethyl, 1-phenylpropyl, cyclohexyl, phenyl, methylphenyl, chlorophenyl, methoxyphenyl, ethoxyphenyl, nitrophenyl, carbamoylphenyl or sulfamoylphenyl. The amide groups may also be N-monosubstituted or N,N-disubstituted and examples of such substituents are alkyl (--CH.sub.3, --C.sub.2 H.sub.5, --C.sub.4 H.sub.9), cyclohexyl or phenyl.
The following radicals are also suitable: ##STR7##
Preferred examples of radical B are: hydrogen, methyl, ethyl, propyl, butyl, .alpha.-ethylpentyl, benzyl, phenylethyl, phenyl which may bear methyl, ethyl, methoxy, ethoxy or chloro as substituents and the radicals of the formulae: ##STR8##
Specific examples of radicals Z.sup.1 to Z.sup.4 and R to R.sup.3 (in addition to those already specified) are:
(1) optionally substituted alkyl: CH.sub.3, C.sub.2 H.sub.5, n--C.sub.3 H.sub.7, i--C.sub.3 H.sub.7, n--C.sub.4 H.sub.9, i--C.sub.4 H.sub.9, C.sub.6 H.sub.13, ##STR9## CH.sub.2 CH.sub.2 OH, (CH.sub.2).sub.3 OH, ##STR10## (CH.sub.2).sub.4 OH (CH.sub.2).sub.6 OH, ##STR11## (CH.sub.2).sub.2 O(CH.sub.2).sub.2 OH, (CH.sub.2).sub.3 O(CH.sub.2).sub.4 OH, (CH.sub.2).sub.3 OC.sub.2 H.sub.4 OH, (CH.sub.2).sub.3 OC.sub.2 H.sub.4 OCH.sub.3, (CH.sub.2).sub.3 OC.sub.2 H.sub.4 OC.sub.2 H.sub.5, (CH.sub.2).sub.3 O(CH.sub.2).sub.6 OH, (CH).sub.3 OC.sub.2 H.sub.4 OCH(CH.sub.3).sub.2, (CH.sub.2).sub.3 OC.sub.2 H.sub.4 OC.sub.4 H.sub.9, (CH.sub.2).sub.3 OC.sub.2 H.sub.4 OCH.sub.2 C.sub.6 H.sub.5, (CH.sub.2).sub.3 OC.sub.2 H.sub.4 OC.sub.2 H.sub.4 C.sub.6 H.sub.5, ##STR12## (CH.sub.2).sub.3 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5, ##STR13## the corresponding radicals in which the groupings: --OC.sub.2 H.sub.4 -- ##STR14## are present twice, three times or four times, CH.sub.2 CH.sub.2 OCH.sub.3, CH.sub.2 CH.sub.2 OC.sub.2 H.sub.5, CH.sub.2 CH.sub.2 OC.sub.3 H.sub.7, CH.sub.2 CH.sub.2 OC.sub.4 H.sub.9, CH.sub.2 CH.sub.2 OC.sub.6 H.sub.5, (CH.sub.2).sub.3 OCH.sub.3, (CH.sub.2).sub.3 OC.sub.2 H.sub.5, (CH.sub.2).sub.3 OC.sub.3 H.sub.7, (CH.sub.2).sub.3 OC.sub.4 H.sub.9, ##STR15## (CH.sub.2).sub.3 OC.sub.6 H.sub.13, (CH.sub.2).sub.3 OC.sub.8 H.sub.17, ##STR16## (CH.sub.2).sub.3 OCH.sub.2 C.sub.6 H.sub.5, (CH.sub.2).sub.3 OC.sub.2 H.sub.4 C.sub.6 H.sub.5, (CH.sub.2).sub.3 OC.sub.6 H.sub.5, ##STR17##
(2) optionally substituted cycloalkyl and polycycloalkyl: ##STR18##
(3) aralkyl: CH.sub.2 C.sub.6 H.sub.5, C.sub.2 H.sub.4 C.sub.6 H.sub.5, ##STR19## and C.sub.6 H.sub.4 CH.sub.3 instead of C.sub.6 H.sub.5.
(4) optionally substituted phenyl: C.sub.6 H.sub.5, C.sub.6 H.sub.4 CH.sub.3, C.sub.6 H.sub.3 (CH.sub.3).sub.2, C.sub.6 H.sub.4 OCH.sub.3, C.sub.6 H.sub.4 OC.sub.2 H.sub.5, ##STR20## C.sub.4 H.sub.4 OCH.sub.2 CH.sub.2 OH or C.sub.6 H.sub.4 Cl.
(5) CH.sub.2 CH.dbd.CH.sub.2, (CH.sub.2).sub.2 COOH, (CH.sub.2).sub.5 COOH and ##STR21## in which n is 2, 3, 4 or 6, C.sub.2 H.sub.4 OCOCH.sub.3, C.sub.2 H.sub.4 OCHO, C.sub.2 H.sub.4 OCOCH.sub.2 COCH.sub.3, (C.sub.2 H.sub.4 O).sub.2 COOH.sub.3, (C.sub.2 H.sub.4 O).sub.2 CHO, (CH.sub.2).sub.3 OCOCH.sub.3, (CH.sub.2).sub.3 OCHO, C.sub.2 H.sub.4 OCOC.sub.2 H.sub.4 COOH.
Examples of radicals R to R.sup.3 containing sulfonic acid groups are (in addition to SO.sub.3 H): CH.sub.2 CH.sub.2 SO.sub.3 H, CH.sub.2 CH.sub.2 OSO.sub.3 H, (CH.sub.2).sub.3 OSO.sub.3 H, ##STR22## (CH.sub.2).sub.4 OSO.sub.3 H, (CH.sub.2).sub.6 OSO.sub.3 H, ##STR23## (CH.sub.2).sub.2 O(CH.sub.2).sub.2 OSO.sub.3 H, (CH.sub.2).sub.3 O(CH.sub.2).sub.2 OSO.sub.3 H, (CH.sub.2).sub.3 O(CH.sub.2).sub.4 OSO.sub.3 H, (CH.sub.2).sub.3 OC.sub.2 H.sub.4 OCH.sub.2 C.sub.6 H.sub.4 SO.sub.3 H, (CH.sub.2).sub.3 OC.sub.2 H.sub.4 OC.sub.2 H.sub.4 C.sub.6 H.sub.4 SO.sub.3 H, (CH.sub.2).sub.3 OC.sub.2 H.sub.4 OC.sub.6 H.sub.4 SO.sub.3 H, CH.sub.2 CH.sub.2 OC.sub.6 H.sub.4 SO.sub.3 H, (CH.sub.2).sub.3 OC.sub.6 H.sub.4 SO.sub.3 H, (CH.sub.2).sub.3 OCH.sub.2 C.sub.6 H.sub.4 SO.sub.3 H, (CH.sub.2).sub.3 OC.sub.2 H.sub.4 C.sub.6 H.sub.4 SO.sub.3 H, ##STR24## CH.sub.2 C.sub.6 H.sub.4 SO.sub.3 H, C.sub.2 H.sub.4 C.sub.6 H.sub.4 SO.sub.3 H, ##STR25##
Examples of substituents R to R.sup.3 which are preferred are: hydrogen, CH.sub.3, C.sub.2 H.sub.5, n--C.sub.3 H.sub.7, i--C.sub.3 H.sub.7, n--C.sub.4 H.sub.9, i--C.sub.4 H.sub.9, C.sub.6 H.sub.13, CH.sub.2 CH.sub.2 OH, (CH.sub.2).sub.3 OH, ##STR26## (CH.sub.2).sub.4 OH, (CH.sub.2).sub.6 OH, ##STR27## (CH.sub.2).sub.2 O(CH.sub.2).sub.2 OH, (CH.sub.2).sub.3 O(CH.sub.2).sub.2 OH, (CH.sub.2).sub.3 O(CH.sub.2).sub.4 OH, (CH.sub.2).sub.3 O(CH.sub.2).sub.6 OH, ##STR28## CH.sub.2 CH.sub.2 OCH.sub.3, CH.sub.2 CH.sub.2 OC.sub.2 H.sub.5, CH.sub.2 CH.sub.2 OC.sub.4 H.sub.9, (CH.sub.2).sub.3 OCH.sub.3, (CH.sub.2).sub.3 OC.sub.2 H.sub.5, (CH.sub.2).sub.3 OC.sub.3 H.sub.7, (CH.sub.2).sub.3 OC.sub.4 H.sub.9, (CH.sub.2).sub.3 OC.sub.6 H.sub.13, (CH.sub.2).sub.3 OC.sub.8 H.sub.17, ##STR29## (CH.sub.2).sub.3 OC.sub.2 H.sub.4 OCH.sub.3, (CH.sub.2).sub.3 OC.sub.2 H.sub.4 OC.sub.4 H.sub.9, (CH.sub.2).sub.3 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5, ##STR30## CH.sub.2 C.sub.6 H.sub.5, C.sub.2 H.sub.4 C.sub.6 H.sub.5, ##STR31## C.sub.6 H.sub.5, C.sub.6 H.sub.4 CH.sub.3, C.sub.6 H.sub.3 (CH.sub.3).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 OH, C.sub.6 H.sub.4 Cl, CH.sub.2 CH.sub.2 SO.sub.3 H, CH.sub.2 CH.sub.2 OSO.sub.3 H, (CH.sub.2).sub.3 OSO.sub.3 H, ##STR32## (CH.sub.2).sub.4 OSO.sub.3 H, (CH.sub.2).sub.6 OSO.sub.3 H, (CH.sub.2).sub.2 O(CH.sub.2).sub.2 OSO.sub.3 H, (CH.sub.2).sub.3 O(CH.sub.2).sub.2 OSO.sub.3 H, (CH.sub.2).sub.3 O(CH.sub.2).sub.4 OSO.sub.3 H, (CH.sub.2).sub.3 O(CH.sub.2).sub.6 OSO.sub.3 H, (CH.sub.2).sub.3 OC.sub.6 H.sub.4 SO.sub.3 H, (CH.sub.2).sub.3 OCH.sub.2 C.sub.6 H.sub.4 SO.sub.3 H, (CH.sub.2).sub.3 OC.sub.2 H.sub.4 C.sub.6 H.sub.4 SO.sub.3 H, CH.sub.2 C.sub.6 H.sub.4 SO.sub.3 H, C.sub.2 H.sub.4 C.sub.6 H.sub.4 SO.sub.3 H, ##STR33##
Dyes are alo preferred in which two radicals R together with the nitrogen form the radical of pyrrolidine, piperidine or morpholine.
The dyes of formula (I) may be prepared or used in the form of the free acids or conveniently as water-soluble salts, for example as alkali metal, ammonium or substituted ammonium salts. Examples of substituted ammonium cations in the salts are trimethylammonium, methoxyethylammonium, hexoxypropylammonium or dimethylphenylbenzylammonium.
Dyes of formula (I) may be prepared by reacting a diazo compound of an amine of formula (V):
d--nh.sub.2 (v)
with a coupling component of formula (VI):
h--a (vi),
d and/or HA normally containing at least one sulfonic acid group. Diazotization and coupling are carried out by conventional methods. The new dyes, particularly those having sulfuric acid hemiester groups may also be obtained by first preparing the compounds devoid of SO.sub.3 H groups and then converting these with a sulfonating agent such as concentrated sulfuric acid, sulfuric acid monohydrate or oleum into the dye of formula (I). The Examples may be referred to for details. Coupling components of the formula H--A and their production are known from German Laid Open Specification No. 22 02 820.
Examples of compounds of the formula (V) are: aniline, 2-chloroaniline, 3-chloroaniline, 4-chloroaniline, 2-bromoaniline, 3-bromoaniline, 4-bromoaniline, 2-nitroaniline, 3-nitroaniline, 4-nitroaniline, 2-toluidine, 3-toluidine, 4-toluidine, 2-cyanoaniline, 3-cyanoaniline, 4-cyanoaniline, 2,4-dicyanoaniline, 3,4-dichloroaniline, 2,5-dichloroaniline, 2,4,5-trichloroaniline, 2,4,6-trichloroaniline, 2-chloro-4-nitroaniline, 2-bromo-4-nitroaniline, 2-cyano-4-nitroaniline, 2-methylsulfonyl-4-nitroaniline, 4-chloro-2-nitroaniline, 4-methyl-2-nitroaniline, 2-methoxy-4-nitroaniline, 1-amino-2-trifluoromethyl-4-chlorobenzene, 2-chloro-5-aminobenzonitrile, 2-amino-5-chlorobenzonitrile, 1-amino-2-nitrobenzene-4-sulfonic acid n-butylamide or .beta.-methoxyethylamide, 1-aminobenzene-4-methylsulfone, 1-amino-2,6-dibromobenzene-4-methylsulfone, 1-amino-2,6-dichlorobenzene-4-methylsulfone, the methyl, propyl, .beta.-methoxyethyl or butyl ester of 3,5-dichloroanthranilic acid, the methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, or .beta.-methoxyethyl ester of 3,5-dibromoanthranilic acid, N-acetyl-p-phenylenediamine, N-acetyl-m-phenylenediamine, N-benzenesulfonyl-p-phenylenediamine, 4-aminoacetophenone, 4-aminobenzophenone, 2-aminobenzophenone, 2-aminodiphenylsulfone, 4-aminodiphenylsulfone, the methyl, ethyl, propyl, butyl, isobutyl, .beta.-methoxyethyl, .beta.-ethoxyethyl, methyl diglycol, ethyl diglycol or methyl triglycol ester of 2-aminobenzoic acid or 3-aminobenzoic acid or 4-aminobenzoic acid, 3-aminophthalic acid, 4-aminophthalic acid, the dimethyl, diethyl, dipropyl or dibutyl ester of 5-aminoisophthalic or aminoterephthalic acid, the amide, methylamide, propylamide, butylamide, isobutylamide, cyclohexylamide, .beta.-ethylhexylamide or .gamma.-methoxypropylamide of 3-aminobenzoic acid or 4-aminobenzoic acid, the dimethylamide, diethylamide, pyrrolidide or morpholide of 2-aminobenzoic acid, 3-aminobenzoic acid or 4-aminobenzoic acid, the diamide of 5-aminoisophthalic acid, the imide, .beta.-hydroxyethylimide, methylimide, ethylimide or tolylimide of 3-aminophthalic acid or 4-aminophthalic acid, the dimethylamide, diethylamide, pyrrolidide or morpholide of 4-aminobenzenesulfonic acid, the hydrazide of 3-aminophthalic acid or 4-aminophthalic acid, the ethylimide, butylimide or methoxyethylimide or 4-aminonaphthalic acid, 1-aminoanthraquinone, 4-aminodiphenylene oxide, 2-aminobenzothiazole, 4-nitronaphthylamine, 5-nitronaphthylamine, 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, 4'-chloro-2-methyl-5-methoxy-4-aminoazobenzene, 4'-nitro-2-methyl-5-methoxy-4-aminoazobenzene, 4'-chloro-2-methyl-4-aminoazobenzene, 2,5-dimethoxy-4-aminoazobenzene, 4'-chloro-2,5-dimethoxy-4-aminoazobenzene, 4'-nitro-2,5-dimethoxy-4-aminoazobenzene, 4'-chloro-2,5-dimethyl-4-aminobenzene, 4'-methoxy-2,5-dimethyl-4-aminoazobenzene, 4'-nitro-4-aminoazobenzene, 3,5-dibromo-4-aminoazobenzene, 2,3'-dichloro-4-aminoazobenzene, 3-methoxy-4-aminoazobenzene, 1-aminobenzene-2-sulfonic acid, 1-aminobenzene-3-sulfonic acid, 1-aminobenzene-4-sulfonic acid, 1-aminobenzene-2,4-disulfonic acid, 1-aminobenzene-2,5-disulfonic acid, 1-amino-2-methylbenzene-4-sulfonic acid, 1-amino-3-methylbenzene-4-sulfonic acid, 1-amino-4-methylbenzene-2-sulfonic acid, 1-amino-4-methylbenzene-3-sulfonic acid, 2-nitraooaniline-4-sulfonic acid, 4-nitroaniline-2-sulfonic acid, 2-chloroaniline-4-sulfonic acid, 2-chloroaniline-5-sulfonic acid, 3-chloroaniline-6-sulfonic acid, 4-chloroaniline-2-sulfonic acid, 1-amino-3,4-dichlorobenzene- 6-sulfonic acid, 1-amino-2,5-dichlorobenzene-4-sulfonic acid, 1-amino-4-methyl-5-chlorobenzene-2-sulfonic acid, 1-amino-3-methyl-4-chlorobenzene-6-sulfonic acid 2-amino-4-sulfobenzoic acid, 1-amino-4-acetaminobenzene-2-sulfonic acid, 1-amino-5-acetaminobenzene-2-sulfonic acid, 1-amino-2-methoxy-4-nitrobenzene-5-sulfonic acid, 1-aminoanthraquinone-2-sulfonic acid, 1-aminonaphthalene-2-sulfonic acid, 1-aminonaphthalene-4-sulfonic acid, 2-aminonaphthalene-1-sulfonic acid, and the diazo components of the formulae: ##STR34##
Particular industrial significance attaches to dyes of the formula (Ia):
D.sup.1 --N.dbd.N--A.sup.1 (Ia)
in which D.sup.1 is: ##STR35##
p is zero or 1;
Y is hydrogen, cyano, chloro, bromo, methylsulfone, ethylsulfone, phenylsulfone, carbalkoxy or SO.sub.3 H;
Y.sup.1 is hydrogen, chloro, bromo or SO.sub.3 H;
Y.sup.2 is hydrogen, chloro, bromo, methyl, carbalkoxy, 2-benzothiazolyl or SO.sub.3 H;
X is hydrogen, methyl, hydroxy, methoxy or SO.sub.3 H;
X.sup.1 is hydrogen, methyl, methoxy or SO.sub.3 H;
X.sup.2 is hydrogen, methyl or methoxy;
T is hydrogen or a substituent; and
A.sup.1 has the above meanings.
Preferred radicals T are alkyls of two to eight carbon atoms which may be interrupted by oxygen and may bear hydroxy, phenoxy or OSO.sub.3 H as a substituent, benzyl, benzyl bearing SO.sub.3 H as a substituent, phenylethyl, phenylethyl bearing SO.sub.3 H as a substituent, and phenyl which may bear SO.sub.3 H and/or other radicals as a substituent.
Examples of radicals T are: CH.sub.3, C.sub.2 H.sub.5, C.sub.3 H.sub.7, C.sub.4 H.sub.9, C.sub.6 H.sub.13, ##STR36## CH.sub.2 CH.sub.2 OH, (CH.sub.2).sub.3 OH, CH.sub.2 CH.sub.2 OCH.sub.2 CH.sub.2 OH, (CH.sub.2).sub.3 O(CH.sub.2).sub.4 OH, CH.sub.2 CH.sub.2 OC.sub.6 H.sub.5, CH.sub.2 CH.sub.2 OSO.sub.3 H, (CH.sub.2).sub.3 OSO.sub.3 H, CH.sub.2 CH.sub.2 OCH.sub.2 CH.sub.2 OSO.sub.3 H, (CH.sub.2).sub.3 O(CH.sub.2).sub.4 OSO.sub.3 H, CH.sub.2 C.sub.6 H.sub.5, CH.sub.2 C.sub.6 H.sub.4 SO.sub.3 H, C.sub.2 H.sub.4 C.sub.6 H.sub.5, C.sub.2 H.sub.4 C.sub.6 H.sub.4 SO.sub.3 H, C.sub.6 H.sub.5, C.sub.6 H.sub.4 SO.sub.3 H, ##STR37##
Preferred radicals for R and R.sup.3 in the radicals A.sup.1 in dyes of the formula (Ia) are alkyl of one to eight carbon atoms which may be interrupted by oxygen and may bear hydroxy, phenoxy, benzoyloxy or OSO.sub.3 H as a substituent, benzyl, phenylethyl or benzyl or phenylethyl bearing SO.sub.3 H as a substituent, unsubstituted or substituted phenyl or hydroxysulfonylphenyl radicals or hydrogen. Preferred also are dyes in which the radical A.sup.1 corresponds to the formula (IVb) and in which R and R.sup.1 together with the nitrogen form the radical of pyrrolidine, piperidine or morpholine.
The SO.sub.3 H groups may be situated preferably either only in the radical D or only in the radical Z, particularly when Z contains a phenyl radical.
Examples of preferred diazo components are: the methyl, ethyl, n-propyl, isopropyl, .beta.-methoxyethyl esters of 2-aminobenzoic, 3-aminobenzoic and 4-aminobenzoic acid, the methyl, ethyl or isopropyl ester of 2-amino-3,5-dichlorobenzoic acid, the methyl, ethyl or .beta.-methoxyethyl ester of 2-amino-3,5-dibromobenzoic acid, ethyl 3-bromo-4-aminobenzoate, diethyl aminoterephthalate, 2-aminobenzonitrile, 2,4-dicyanoaniline, 2-amino-5-chlorobenzonitrile, 2-amino-5-bromobenzonitrile, 2-amino-3-bromo-5-chlorobenzonitrile, 2-amino-3,5-dibromobenzonitrile, 2-amino-3,5-dichlorobenzonitrile, 2-amino-1-trifluoromethylbenzene, 2-amino-5-chlorotrifluoromethylbenzene, 4-aminobenzene-1-methylsulfone, 3-chloro-4-aminobenzene-1-methylsulfone, 2-aminodiphenylsulfone, 4-aminodiphenylsulfone, the .beta.-hydroxyethylimide of 3-aminophthalic or 4-aminophthalic acid, the .beta.-methoxyethylimide of 3-aminophthalic or 4-aminophthalic acid, the butylimide or tolylimide of 3-aminophthalic acid or 4- aminophthalic acid, 1-amino-4-nitrobenzene, 1-amino-4-acetylaminobenzene, 1-amino-3-acetylaminobenzene, 4-aminobenzoic acid amide, the N-methylamide, N-butylamide or N-.beta.-ethylhexylamide of 4-aminobenzoic acid, the N,N-diethylamide of 4-aminobenzoic acid, the amide of 3-aminobenzenesulfonic acid or 4-aminobenzenesulfonic acid, the N-butylamide of 2-aminobenzenesulfonic acid or 4-aminobenzenesulfonic acid, the morpholide of 3-aminobenzenesulfonic acid or 4-aminobenzenesulfonic acid, 2-chloroaniline-4-sulfonic acid, 2-chloroaniline-5-sulfonic acid, 3-chloroaniline-6-sulfonic acid, 4-chloroaniline-2-sulfonic acid, 1-amino-3,4-dichlorobenzene-6-sulfonic acid, 1-amino-2,5-dichlorobenzene-4-sulfonic acid, 1-amino-2,5-dibromobenzene-4- sulfonic acid, 1-amino-4-methyl-5-chlorobenzene-2-sulfonic acid, 1-amino-3-methyl-4-chlorobenzene-6-sulfonic acid and the amines of the formulae: ##STR38## E .dbd. H, CH.sub.3, C.sub.2 H.sub.5.
The new dyes are yellow to violet, have very high color strength and are suitable for dyeing natural and synthetic polyamides such as wool, silk, nylon 6 or nylon 6,6. Brilliant colorations having excellent fastness properties are obtained with them. Individual fastness properties which should be mentioned are those given in the Color Index for Acid Dyes, in particular light fastness, fastness to rubbing milling, perspiration, potting, water, sea water and washing. The dyes also have very good solubilities, good levelling power and build-up, and the dyeing behavior is essentially independent of the pH.





The following Examples illustrate the invention. References to parts and percentages in the following Examples are by weight unless stated otherwise.
EXAMPLE 1
18 parts of 4-aminoazobenzene-3,4'-disulfonic acid is dissolved in 125 parts by volume of water while hot with an addition of 4 parts of sodium hydroxide. The calculated amount of a 23% sodium nitrite solution is added and then the whole is then added to a mixture of 15 parts by volume of concentrated hydrochloric acid, 100 parts by volume of water and 150 parts of ice. The suspension is stirred for another three hours to complete the diazotization and then added to a solution of 15 parts of 2-phenyl-4,6-bis-.gamma.-hydroxypropylaminopyrimidine in 100 parts by volume of dimethylformamide and 500 parts by volume of ice water. After a pH of 4 to 5 has been set up the mixture is stirred until coupling is completed. The dye of the formula: ##STR39## is then precipitated with common salt, filtered, washed with a dilute solution of common salt and dried. The product dyes polyamide material, for example fibers of poly-.epsilon.-caprolactam red hues having very good fastness to light and wet treatment.
EXAMPLE 2
8.3 parts of 4-aminoazobenzene-4'-sulfonic acid is dissolved neutral in 75 parts by volume of water at 70.degree. C., 9 parts by volume of a 23% sodium nitrite solution is added and the solution obtained is then cooled by adding ice to 10.degree. C. The mixture is then acidified with 9 parts by volume of concentrated hydrochloric acid and stirred at ambient temperature until diazotization is over. The suspension is then added to 9.2 parts of 2-piperidino-4-methyl-6-hydroxyethoxyethylaminopyrimidine which has previously been dissolved in 100 parts by volume of formamide, 20 parts by volume of dilute hydrochloric acid and 500 parts by volume of ice-water. Coupling is carried out at a pH of 6.5 to 7. After the reaction is over the pH of the solution is adjusted to 8, the dye which in the form of the free acid corresponds to the formula: ##STR40## is precipitated with sodium chloride and isolated in the usual way. An orange brown powder is obtained which colors polyamide orange hues having good light and wet fastness properties.
EXAMPLE 3
A solution of 12 parts of 2,5-dichlorosulfanilic acid in 120 parts by volume of dilute caustic soda solution (pH 8) is united with the calculated amount of a 23% sodium nitrite solution and added to 9 parts by volume of concentrated hydrochloric acid and 100 parts of ice. Diazotization is over within two hours at 0.degree. to 5.degree. C. The suspension obtained is added to a mixture of 8.6 parts of 2-phenyl-4-.beta.-hydroxyethylamino-6-.beta.-methoxyethylaminopyrimidine (previously dissolved in dilute hydrochloric acid) and 200 parts of ice and the whole is adjusted with 10% caustic soda solution to a pH of 6 to 7 and stirred overnight. The deposited dye is brought into solution by heating at pH 10, the dye salt is precipitated with sodium chloride, filtered off and dried. The dye in the form of the free acid corresponds to the formula: ##STR41## it dyes polyamide materials yellow hues of outstanding light and wet fastness properties.
EXAMPLE 4
9 parts of the coupling product of sulfanilic acid and 2,5-dimethylaniline is diazotized in the usual way in 200 parts by volume of water in the presence of 10 parts by volume of concentrated hydrochloric acid with sodium nitrite at ambient temperature. The diazotization mixture is then coupled with a solution of 8.6 parts of 2-phenyl-4-.beta.-hydroxyethylamino-6-.beta.-methoxyethylaminopyrimidine in 100 parts by volume of formamide and 250 parts of ice, the pH being adjusted to 5.5 and the mixture stirred until coupling is over. The deposited dye is then filtered off, dissolved in dilute caustic soda solution, again precipitated with sodium chloride, filtered off and dried. The compound corresponds in the form of the free acid to the formula: ##STR42## It dyes polyamide materials yellowish red hues of outstanding fastness properties.
The following dyes are also prepared by methods analogous to those described in the foregoing Examples.
__________________________________________________________________________ ##STR43## Hue of dyeingEx. on poly-No. DK X.sup.1 X.sup.2 X.sup.3 amide__________________________________________________________________________ 5 ##STR44## ##STR45## NHC.sub.2 H.sub.4 OCH.sub.3 NHC.sub.2 H.sub.4 OCH.sub.3 yellow 6 " " NHC.sub.2 H.sub.4 OH NHC.sub.2 H.sub.4 OH yellow 7 " ##STR46## CH.sub.3 NH(CH.sub.2).sub.3 OCH.sub.3 yellow 8 " " " NHC.sub.2 H.sub.4 OH yellow 9 ##STR47## " " " yellow10 " " " NH(CH.sub.2).sub.3 OCH.sub.3 yellow11 " ##STR48## NHC.sub.2 H.sub.4 OCH.sub.3 NHC.sub.2 H.sub.4 OCH.sub.3 yellow12 " " NHC.sub.2 H.sub.4 OH NHC.sub.2 H.sub.4 OH yellow13 ##STR49## " " " yellow14 " " NHC.sub.2 H.sub.4 OCH.sub.3 NHC.sub.2 H.sub.4l yellowb.315 " ##STR50## CH.sub.3 NH(CH.sub.2).sub.3 OCH.sub.3 yellow16 " " " NHC.sub.2 H.sub.4 OH yellow17 ##STR51## " " " yellow18 " " " NH(CH.sub.2).sub.3 OCH.sub.3 yellow19 " ##STR52## NHC.sub.2 H.sub.4 OCH.sub.3 NHC.sub.2 H.sub.4 OCH.sub.3 yellow20 " " NHC.sub.2 H.sub.4 OH NHC.sub.2 H.sub.4 OH yellow21 ##STR53## " " " yellow22 " " NHC.sub.2 H.sub.4 OCH.sub.3 NHC.sub.2 H.sub.4 OCH.sub.3 yellow23 ##STR54## " " NHC.sub.2 H.sub.4 OH yellow24 " ##STR55## CH.sub.3 NH(C.sub.2 H.sub.4 O).sub.2 yellow25 ##STR56## ##STR57## NHC.sub.2 H.sub.4 OH NHC.sub.2 H.sub.4 OH yellow26 " " NH(CH.sub.2).sub.3 OH NH(CH.sub.2).sub.3 OH yellow27 " " NHC.sub.2 H.sub.4 OCH.sub.3 NHC.sub.2 H.sub.4 OCH.sub.3 yellow28 " .varies. NH(CH.sub.2).sub.3 OCH.sub.3 NH(CH.sub.2).sub.3 OCH.sub.3 yellow29 " " NHC.sub.2 H.sub.4 OH NHC.sub.2 H.sub.5 yellow30 " " " NHC.sub. 4 H.sub.9 yellow31 " " " NH.sub.2 yellow32 " " " ##STR58## yellow33 " " NH.sub.2 " yellow34 " " NHC.sub.2 H.sub.4 OH NH(CH.sub.2).sub.3 OCH.sub.3 yellow35 " " " NH(CH.sub.2).sub.3 OC.sub.3 H.sub.7 (i) yellow36 " " NH.sub.2 NH(CH.sub.2).sub.3 O(CH.sub.2) .sub.4 OH yellow37 " " NHC.sub.2 H.sub.4 OH ##STR59## yellow38 " " " ##STR60## yellow39 " " " NH(CH.sub.2).sub.3 OCH.sub.2 C.sub.6 H.sub.5 yellow40 " " " NHCH.sub.2 C.sub.6 H.sub.5 yellow41 " " NH(CH.sub.2).sub.3 OH " yellow42 " " NHC.sub.2 H.sub.4 OH ##STR61## yellow43 " " " NHC.sub.6 H.sub.5 yellow44 " " NH(C.sub.2 H.sub.4 O).sub.2 H " yellow45 " ##STR62## NHC.sub.2 H.sub.4 OH MHC.sub.2 H.sub.4 OH yellow46 " " ##STR63## NH(CH.sub.2).sub.3 OC.sub.3 H.sub.7 (i) yellow47 " ##STR64## ##STR65## NH)h.sub.2).sub.3 OCH.sub.3 yellow48 " ##STR66## NHC.sub.2 H.sub.4 OH NH(CH.sub.2).sub.3 OC.sub.3 H.sub.7 (i)49 " ##STR67## NH(C.sub.2 H.sub.4 O).sub.2 H NH(C.sub.2 H.sub.4 O).sub.2 yellow50 " H NH(CH.sub.2).sub.3 OH NH(CH.sub.2).sub.3 OCH.sub.3 yellow51 " CH.sub.3 NHC.sub.2 H.sub.4 OCH.sub.3 NHC.sub.2 H.sub.4 OCH.sub.3 yellow52 " " NH(CH.sub.2).sub.3 OH ##STR68## yellow53 " CH(CH.sub.3).sub.2 NH(CH.sub.2).sub.3 OCH.sub.3 NH(CH.sub.2).sub.3 OCH.sub.3 yellow54 " C.sub.4 H.sub.9 NH(CH.sub.2).sub.3 OH NH(CH.sub.2).sub.3 OH yellow55 " ##STR69## " " yellow56 " ##STR70## " " yellow57 " CH.sub.2 OCH.sub.2 H.sub.5 " " yellow58 " ##STR71## " " yellow59 " N(C.sub.2 H.sub.5).sub.2 H NHC.sub.6 H.sub.5 yellow60 " ##STR72## CH.sub.3 NHC.sub.2 H.sub.4 OH yellow61 " " " NH(C.sub.2 H.sub.4 O).sub.2 yellow62 " " " NH(CH.sub.2).sub.3 OH yellow63 " " " NH(CH.sub.2 yellow3 OCH.sub.64 " " " NHCH.sub.2 C.sub.6 H.sub.5 yellow65 " N(C.sub.2 H.sub.5).sub.2 " NHC.sub.2 H.sub.4 C.sub.6 H.sub.5 yellow66 ##STR73## ##STR74## NHC.sub.2 H.sub.4 OH NHC.sub.2 H.sub.4 OH yellowish orange67 ##STR75## " " " yellow68 ##STR76## " " " yellow69 ##STR77## " " " yellow70 ##STR78## " " NHC.sub.4 H.sub.9 orange71 " ##STR79## CH.sub.3 NHC.sub.2 H.sub.4 OH yellow72 ##STR80## ##STR81## NHC.sub.2 H.sub.4 OH NHC.sub.2 H.sub.4 OH reddish orange73 " " NH(CH.sub.2).sub.3 OH NH(CH.sub.2).sub.3 OH "74 " " NH(CH.sub.2).sub.3 OCH.sub.3 NH(CH.sub.2).sub.3 OCH.sub.3 "75 " " NHC.sub.2 H.sub.4 OCH.sub.3 NHC.sub.2 H.sub.4 OCH.sub.3 "76 " " NHC.sub.2 H.sub.4 OH NHC.sub.4 H.sub.9 "77 " ##STR82## NH(CH.sub.2).sub.3 OH NH(CH.sub.2).sub.3 OCH.sub.3 "78 " ##STR83## NH(CH.sub.2).sub.3 OCH.sub.3 " orange79 " ##STR84## CH.sub.3 NHC.sub.2 H.sub.4 OH orange80 " " " NH(CH.sub.2).sub.3 OCH.sub.3 "81 ##STR85## ##STR86## NHC.sub.2 H.sub.4 Oh NHC.sub.2 H.sub.4 OH yellowish red82 " " NH(CH.sub.2).sub.3 OH NH(CH.sub.2).sub.3 OH "83 " " NHC.sub.2 H.sub.4 OCH.sub.3 NHC.sub.2 H.sub.4 OCH.sub.3 "84 " " NH(CH.sub.2).sub.3 OCH.sub.3 NH(CH.sub.2).sub.3 OCH.sub.3 "85 " " ##STR87## " "86 " " NH.sub.2 NH.sub.2 orange87 " " NH(CH.sub.2).sub.6 OH NHC.sub.2 H.sub.4 OCH.sub.3 yellowish red88 " " NH(CH.sub.2).sub.3 OC.sub.2 H.sub.4 "H "89 " " NH(CH.sub.2).sub.3 O(CH.sub.2).sub.6 "H "90 " " NHC.sub.2 H.sub.4 OH NH(CH.sub.2).sub.3 OCH.sub.2 C.sub.6 H.sub.5 yellowish red91 " ##STR88## " NHC.sub.4 H.sub.9 "92 " ##STR89## NH(CH.sub.2).sub.3 OCH.sub.3 NH(CH.sub.2).sub.3 OCH.sub.3 "94 " ##STR90## CH.sub.3 NH(C.sub.2 H.sub.4 O).sub.2 COCH.sub.3 orange95 " ##STR91## " " "96 " N(C.sub.3 H.sub.7).sub.2 " " "97 ##STR92## ##STR93## NH.sub.2 NH.sub.2 "98 " " NHC.sub.2 H.sub.4 OH NHC.sub.2 H.sub.4 OH red99 " " NH(C.sub.2 H.sub.4 O).sub.2 H NH(C.sub.2 H.sub.4 O).sub.2 "100 " " NHC.sub.2 H.sub.4 OCH.sub.3 "101 " " NH(CH.sub.2).sub.3 OCH.sub.3 NH(CH.sub.2).sub.3 OCH.sub.3 "102 " " NH.sub.2 ##STR94## red103 " " NHC.sub.2 H.sub.4 OH NHC.sub.2 H.sub.5 "104 " " " NHC.sub.3 H.sub.7105 " " " NHC.sub.3 H.sub.7 "105 " " " NHC.sub.6 H.sub.13 "106 " " NH(CH.sub.2).sub.3 OH NH(CH.sub.2).sub.3 OC.sub.2 H.sub.4 OC.sub.2 H.sub.5 "107 " " " NH(CH.sub.2).sub.3 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5 "108 " " " NH(CH.sub.2).sub.3 OC.sub.2 H.sub.5 "109 " " " NH(CH.sub.2).sub.3 OC.sub.2 H.sub.4 C.sub.6 H.sub.5 "110 " " " ##STR95## "111 " " " ##STR96## "112 " " " ##STR97## "113 " " NH(CH.sub.2).sub.3 O(CH.sub.2).sub.4 NHC.sub.2 H.sub.4 OCH.sub.3 red114 " " NHC.sub.2 H.sub.4 OH NHCH.sub.2 C.sub.6 H.sub.5 "115 " " " NHC.sub.2 H.sub.4 C.sub.6 H.sub.5 "116 " " " NHC.sub.6 H.sub.5 "117 " " NH(CH.sub.2).sub.3 OH ##STR98## "118 " ##STR99## NHC.sub.2 H.sub.4 OH NHC.sub.4 H.sub.9 "119 " ##STR100## NH(CH.sub.2).sub.3 OCH.sub.3 NH(CH.sub.2).sub.3 OCH.sub.3 "120 " ##STR101## NH(CH.sub.2).sub.3 OH NH(CH.sub.2).sub.3 OH "121 " N(C.sub.2 H.sub.5).sub.2 H NHC.sub.2 H.sub.4 OH orange122 " " " NHC.sub.6 H.sub.5 "123 " N(CH.sub.3).sub.2 CH.sub.3 NH(CH.sub.2).sub.3 OH yellowish red124 " N(C.sub.2 H.sub.5).sub.2 " NH(CH.sub.2).sub.3 O(CH.sub.2) .sub.4 OH yellowish red125 " " " ##STR102## "126 " " " NH(CH.sub.2).sub.3 OCH.sub.2 C.sub.6 H.sub.5 "127 " " " ##STR103## "128 " " " ##STR104## "129 " " " NHCH.sub.2 C.sub.6 H.sub.5 "130 " " " ##STR105## "131 " " " ##STR106## "132 " N(C.sub.3 H.sub.7).sub.2 " NH(CH.sub.2).sub.3 OH "133 " " " NHC.sub.2 H.sub.4 C.sub.6 H.sub.5 "134 " ##STR107## " NH(CH.sub.2).sub.3 OH "135 " ##STR108## " " yellowish red136 " ##STR109## " " "137 " ##STR110## " NH(C.sub.2 H.sub.4 O).sub.2 "138 " " " NH(CH.sub.2).sub.3 O(CH.sub.2) .sub.4 OH "139 " " " NHCH.sub.2 C.sub.6 H.sub.5 "140 " " C.sub.3 H.sub.7 NH(CH.sub.2).sub.3 OH "141 " " ##STR111## " "142 " ##STR112## CH.sub.3 " "143 " ##STR113## " " "144 ##STR114## ##STR115## NHC.sub.2 H.sub.4 OH NHC.sub.2 H.sub.4 OH red145 " " NH(CH.sub.2).sub.3 OH NH(CH.sub.2).sub.3 OH "146 " " NH(C.sub.2 H.sub.4 O).sub.2 H NH(C.sub.2 H.sub.4 O).sub.2 "147 " " NHC.sub.2 H.sub.4 OCH.sub.3 NHC.sub.2 H.sub.4 OCH.sub.3 "148 " " NH(CH.sub.2).sub.3 OCH.sub.3 NH(CH.sub.2).sub.3 OCH.sub.3 "149 " ##STR116## CH.sub.3 NHC.sub.2 H.sub.4 OH yellowish red150 ##STR117## ##STR118## NHC.sub.2 H.sub.4 OCH.sub.3 NH(CH.sub.2).sub.3 O(CH.sub.2) .sub.4 OH Bordeaux151 " ##STR119## CH.sub.3 NHC.sub.2 H.sub.4 OH red152 ##STR120## " " " Bordeaux153 " ##STR121## NHC.sub.2 H.sub.4 OH NHC.sub.2 H.sub.4 OCH.sub.3 violet154 " " NHC.sub.2 H.sub.4 OCH.sub.3 NH(CH.sub.2).sub.3 O(CH.sub.2) .sub.4 OH "155 ##STR122## " " " yellowish red156 " ##STR123## CH.sub.3 NHC.sub.2 H.sub.4 OH reddish orange157 ##STR124## " " " red158 " ##STR125## NHC.sub.2 H.sub.4 OH NHC.sub.2 H.sub.4 OCH.sub.3 "159 ##STR126## " NHC.sub.2 H.sub.4 OCH.sub.3 NH(CH.sub.2).sub.3 O(CH.sub.2) .sub.4 OH violet160 " ##STR127## CH.sub.3 NHC.sub.2 H.sub.4 OH Bordeaux161 ##STR128## ##STR129## NHC.sub.2 H.sub.4 OH NHC.sub.2 H.sub.4 OCH.sub.3 yellowish red162 ##STR130## " " " red163 " ##STR131## CH.sub.3 NH(CH.sub.2).sub.3 OH yellowish red164 ##STR132## " " " "165 " ##STR133## NHC.sub.2 H.sub.4 OH NHC.sub.2 H.sub.4 OCH.sub.3 red166 ##STR134## " " " "167 " ##STR135## CH.sub.3 NH(CH.sub.2).sub.3 yellowish red168 ##STR136## " " " orange169 " ##STR137## NHC.sub.2 H.sub.4 OH NHC.sub.2 H.sub.4 OCH.sub.3 red170 ##STR138## " " " "171 ##STR139## " " NHC.sub.2 H.sub.4 OH Bordeaux172 ##STR140## " " " "173 ##STR141## " " " red174 ##STR142## " " " violet175 ##STR143## " " " red__________________________________________________________________________
EXAMPLE 176
12.7 parts of 2-pyrrolidino-4-phenylamino-6-methyl-pyrimidine is introduced into 63 parts of oleum (23%) while cooling and the mixture is stirred for two hours at ambient temperature. The solution is then poured into ice-water. The sulfonation product having the probable formula. ##STR144## is thus precipitated. It is filtered off, washed with water and dried. The yield is 14.5 parts and the melting point of the compound is above 350.degree. C.
3.5 parts of o-aminobenzonitrile is dissolved in 100 parts by volume of water and 10 parts by volume of concentrated hydrochloric acid. 100 parts of ice is added and diazotization is carried out in the usual way with sodium nitrite. The diazonium salt solution obtained is clarified and added at 0.degree. to 5.degree. C. to a solution of 11 parts of the pyrimidine (obtained by the above method) in 100 parts by volume of water, 10 parts of a 10% caustic soda solution and 200 parts of ice. The pH of the mixture is then adjusted to 6 to 7. After coupling is over the dye whose composition corresponds to the probable formula: ##STR145## is brought into solution by adding caustic soda solution, precipitated with sodium chloride, filtered off and dried. An orange powder is obtained which colors polyamide cloth yellow hues having very good fastness properties.
EXAMPLE 177
15.8 parts of 2-p-tolyl-4,6-bis-.beta.-methoxyethylaminopyrimidine is introduced with slight cooling into 79 parts of oleum (23%) and the mixture is stirred at 35.degree. C. until sulfonation is completed according to a chromatogram. The mixture is then poured into ice-water, the solution is adjusted to pH 7.2 with potassium hydroxide and the potassium salt of the sulfonic acid of the formula: ##STR146## is precipitated with potassium chloride. The product is filtered off, washed with a small amount of water and dried.
12 parts of the compound thus obtained is dissolved in 100 parts by volume of water and 10 parts by volume of a 10% caustic soda solution, then 200 parts of ice is added and coupling is carried out with a solution of the diazonium salt of 3.5 parts of o-aminobenzonitrile. Coupling is over at pH 6 to 7 within a short time. The dye is brought into solution by adding caustic soda solution and the sodium salt is then precipitated with sodium chloride. After isolation in the usual way the dye which in the form of the free acid corresponds to the formula: ##STR147## is obtained as a yellowish brown powder. It dyes polycaprolactam cloth fast yellow hues.
EXAMPLE 178
17 parts of 2-dibutylamino-4-methyl-6-phenylethylaminopyrimidine is introduced into 85 parts of oleum (23%) and heated for three hours at 60.degree. C. The solution is then poured into ice-water. The supernatant aqueous phase is decanted off from the deposited product of the formula: ##STR148## and the compound is dissolved in dilute caustic soda solution.
An aliquot portion of this mixture is coupled with the solution of the diazonium salt of 3.5 parts of o-aminobenzonitrile. The pH is brought to 6 to 7 and the reaction mixture is stirred until coupling has been completed. The precipitated dye of the formula: ##STR149## is then brought into solution with caustic soda solution and precipitated again with sodium chloride. After having been filtered off and dried an orange powder is obtained which colors polycaprolactam material yellow hues which are fast to light and wet.
EXAMPLE 179
24.8 parts of the coupling product from p-aminoazobenzene and 2-phenyl-4-.beta.-hydroxyethylamino-6-.beta.-methoxyethylaminopyrimidine is dissolved in 165 parts of oleum (23%) and the mixture is stirred for three hours at ambient temperature. The solution is then poured into water, the mixture is heated for ninety minutes at 75.degree. C. and the sulfonation product is filtered off and dissolved in dilute caustic soda solution. The solution is filtered and sodium chloride is added to it.
The dye is thus precipitated. In the form of the free acid it has the formula: ##STR150## It is filtered off, washed with a small amount of water and dried. The brown powder obtained dyes polyamide cloth orange hues.
The methods described in Examples 1 to 4 and in Examples 176 to 179 may also be used for the production of the dyes set out in the following Table:
Ex. No. DK X.sup.1 X.sup.2 X.sup.3 Hue 180 ##STR151## ##STR152## NHC.sub.2 H.sub.5 NHC.sub.2 H.sub.5 yellow 181 ##STR153## " " " " 182 " N(C.sub.2 H.sub.5).sub.2 CH.sub.3 NHC.sub.6 H.sub.4 SO.sub.3 H " 183 ##STR154## ##STR155## NHC.sub.2 H.sub.4 OH NHC.sub.2 H.sub.4 OCH.sub.3 orange 184 ##STR156## " " " " 185 ##STR157## " " " reddish yellow 186 " ##STR158## CH.sub.3 NHC.sub.2 H.sub.4 C.sub.6 H.sub.4 SO.sub.3 H yellow 187 ##STR159## ##STR160## NH.sub.2 NH.sub.2 " 188 " " " NHC.sub.2 H.sub.4 OH " 189 " " " NH(CH.sub.2).sub.3 OCH.sub.3 " 190 " " NHC.sub.2 H.sub.4 OH NHC.sub.2 H.sub.5 reddish yellow 191 " " " NH(CH.sub.2).sub.3 OCH.sub.3 " 192 " " " NHC.sub.6 H.sub.5 orange 193 " N(C.sub.2 H.sub.5).sub.2 H NHC.sub.2 H.sub.4 C.sub.6 H.sub.4 SO.sub.3 H yellow 194 " " CH.sub.3 NHCH.sub.2 C.sub.6 H.sub.4 SO.sub.3 H " 195 " ##STR161## " NHC.sub.2 H.sub.4 OCH.sub.3 " 196 " N(C.sub.2 H.sub.5).sub.2 " NH(CH.sub.2).sub.3 OCH.sub.2 C.sub.6 H.sub.4 SO.sub.3 H " 197 ##STR162## ##STR163## NHC.sub.2 H.sub.4 OH NH(CH.sub.2).sub.3 OCH.sub.3 reddishyellow 198 ##STR164## " " " " 199 ##STR165## " " NHC.sub.2 H.sub.4 OH orange 200 " " NH(C.sub.2 H.sub.4 O).sub.2 H NH(C.sub.2 H.sub.4 O).sub.2 H " 201 ##STR166## " NHC.sub.2 H.sub.5 NHC.sub.2 H.sub.5 " 202 " " NHC.sub.2 H.sub.4 OH NHC.sub.6 H.sub.5 " 203 " N(C.sub.2 H.sub.5).sub.2 CH.sub.3 NH(CH.sub.2).sub.3 OCH.sub.3 reddish yellow 204 " " " NHCH.sub.2 C.sub.6 H.sub.5 " 205 " ##STR167## " NH(CH.sub.2).sub.3 O(CH.sub.2).sub.4 OH " 206 ##STR168## ##STR169## NHC.sub.2 H.sub.4 OH NHC.sub.2 H.sub.4 OH " 207 ##STR170## ##STR171## " NHCH.sub.2 C.sub.6 H.sub.4 SO.sub.3 H yellow 208 " ##STR172## NH.sub.2 NH.sub.2 " 209 " " NH.sub.2 NH(CH.sub.3).sub.2 O(CH.sub.2).sub.4 OH " 210 " " NHC.sub.2 H.sub.4 OH NHC.sub.2 H.sub.5 " 211 " " " NH(CH.sub.2).sub.3 OCH.sub.3 " 212 " " " NHC.sub.6 H.sub.4 SO.sub.3 H " 213 " " NH(CH.sub.2).sub.3 OH " " 214 " " NHC.sub.2 H.sub.4 OH NHC.sub.6 H.sub.5 " 215 " " " NH(CH.sub.2).sub.3 OC.sub.2 H.sub.4 C.sub.6 H.sub.5 " 216 " " " NH(CH.sub.2).sub.3 OC.sub.2 H.sub.4 OCH.sub.3 " 217 " " NHC.sub.2 H.sub.4 OCOCH.sub.3 " " 218 " " NHC.sub.2 H.sub.4 OH ##STR173## " 219 " " " ##STR174## " 220 " " NHC.sub.2 H.sub.5 NHC.sub.6 H.sub.3 (OCH.sub.3)SO.sub.3 H " 221 " ##STR175## NH(CH.sub.2).sub.3 OH NH(CH.sub.2).sub.3 OC.sub.3 H.sub.7 (i) " 222 " ##STR176## " NH(CH.sub.2).sub.3 OCH.sub.3 " 223 " ##STR177## NH(C.sub.2 H.sub.4 O).sub.2 H NH(C.sub.2 H.sub.4 O).sub.2 H " 224 " CH.sub.3 NHC.sub.6 H.sub.4 SO.sub.3 H NHC.sub.2 H.sub.4 OCH.sub.3 " 225 " CH(CH.sub.3).sub.2 NHC.sub.2 H.sub.4 C.sub.6 H.sub.4 SO.sub.3 H " " 226 " ##STR178## NH(CH.sub.2).sub.3 OH NH(CH.sub.2).sub.3 OH " 227 " N(C.sub.2 H.sub.5).sub.2 H NHC.sub.6 H.sub.4 SO.sub.3 H " 228 " " CH.sub.3 NHC.sub.2 H.sub.4 C.sub.6 H.sub.4 SO.sub.3 H " 229 " ##STR179## " NHCH.sub.2 C.sub.6 H.sub.4 SO.sub.3 H " 230 ##STR180## " " " " 231 " N(C.sub.2 H.sub.5).sub.2 " NHC.sub.2 H.sub.4 C.sub.6 H.sub.4 SO.sub.3 H " 232 " ##STR181## NHC.sub.2 H.sub.4 OH NH(CH.sub.2).sub.3 OCH.sub.3 " 233 " " " NHC.sub.6 H.sub.5 " 234 " " NH(CH.sub.2).sub.3 OH NHC.sub.6 H.sub.4 SO.sub.3 H " 235 " " NHC.sub.2 H.sub.4 OH NHC.sub. 2 H.sub.4 OH " 236 " " NHC.sub.2 H.sub.4 OCOCH.sub.3 NHC.sub.2 H.sub.4 OCOCH.sub.3 " 237 " " ##STR182## ##STR183## " 238 " " NHC.sub.2 H.sub.4 OCOCH.sub.2 COCH.sub.3 NHC.sub.2 H.sub.4 OCOCH.sub.2 COCH.sub.3 " 239 ##STR184## " NHC.sub.2 H.sub.4 OH NHC.sub.2 H.sub.4 OH orange 240 ##STR185## ##STR186## " NHC.sub.6 H.sub.4 SO.sub.3 H " 241 ##STR187## " " " yellow 242 ##STR188## ##STR189## NHC.sub.2 H.sub.5 NHC.sub. 2 H.sub.5 orange 243 " " NH(C.sub.2 H.sub.4 O).sub.2 H NHC.sub.2 H.sub.4 OCH.sub.3 " 244 " ##STR190## CH.sub.3 NHCH.sub.2 C.sub.6 H.sub.4 SO.sub.3 H " 245 ##STR191## ##STR192## NHC.sub.2 H.sub.4 OH NHC.sub.2 H.sub.4 OH reddishyellow 246 " " NHC.sub.2 H.sub.4 OH NHCH.sub.2 C.sub.6 H.sub.4 SO.sub.3 H " 247 " N(C.sub.2 H.sub.5).sub.2 CH.sub.3 NHC.sub.2 H.sub.4 C.sub.6 H.sub.4 SO.sub.3 H yellow 248 " CH.sub.3 NHC.sub.2 H.sub.4 C.sub.6 H.sub.4 SO.sub.3 H NHC.sub.2 H.sub.4 OCH.sub.3 " 249 ##STR193## ##STR194## NHC.sub.2 H.sub.4 OH NHC.sub.2 H.sub.4 OH reddishyellow 250 ##STR195## " NHC.sub.2 H.sub.5 NHC.sub.2 H.sub.5 yellow 251 " ##STR196## NHC.sub.2 H.sub.4 OH NHC.sub.2 H.sub.4 OH " 252 ##STR197## ##STR198## NHC.sub.2 H.sub.4 OH NH(CH.sub.2).sub.3 OCH.sub.2 C.sub.6 H.sub.4 SO.sub.3 H " 253 " N(C.sub.2 H.sub.5).sub.2 CH.sub.3 NHC.sub.2 H.sub.4 C.sub.6 H.sub.4 SO.sub.3 H " 254 " CH.sub.3 NHC.sub.2 H.sub.4 OCH.sub.3 " " 255 ##STR199## ##STR200## NHC.sub.2 H.sub.4 OH NH(CH.sub.2).sub.3 OCH.sub.2 C.sub.6 H.sub.4 SO.sub.3 H " 256 ##STR201## " " NHC.sub.2 H.sub.4 OCH.sub.3 orange 257 ##STR202## " " " yellow 258 " N(C.sub.2 H.sub.5).sub.2 CH.sub.3 NHC.sub.2 H.sub.4 C.sub.6 H.sub.4 SO.sub.3 H " 259 ##STR203## ##STR204## NHC.sub.2 H.sub.4 OH NHC.sub.2 H.sub.4 OH " 260 " " " NHCH.sub.2 C.sub.6 H.sub.4 SO.sub.3 H " 261 ##STR205## " " NHC.sub.2 H.sub.4 OH " 262 ##STR206## " " " " 263 ##STR207## " " " " 264 " ##STR208## CH.sub.3 NHCH.sub.2 C.sub.6 H.sub.4 SO.sub.3 H " 265 ##STR209## ##STR210## NHC.sub.2 H.sub.4 OH NHC.sub.2 H.sub.4 OH " 266 " " NHC.sub.2 H.sub.4 OCOCH.sub.3 NHC.sub.2 H.sub.4 OCOCH.sub.3 " 267 " " NHC.sub.2 H.sub.4 OH NH(CH.sub.2).sub.3 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5 " 268 " " NH(CH.sub.2).sub.3 OH NHC.sub.6 H.sub.4 SO.sub.3 H " 269 ##STR211## " NH.sub.2 NHC.sub.2 H.sub.4 OH orange 270 " " NHC.sub.2 H.sub.4 OH NH(CH.sub.2).sub.3 OCH.sub.3 reddish orange 271 " " " NH(CH.sub.2).sub.3 OCH.sub.2 C.sub.6 H.sub.4 SO.sub.3 H " 272 " " " NHC.sub.2 H.sub.5 " 273 " " " ##STR212## " 274 " " " ##STR213## " 275 " " ##STR214## ##STR215## " 276 " " NH(CH.sub.2).sub.4 OH NHC.sub.2 H.sub.4 OCH.sub.3 " 277 " " NH(CH.sub.2).sub.6 OH " " 278 " " NH(CH.sub.2).sub.3 O(CH.sub.2).sub.4 OH " " 279 " " NHC.sub.2 H.sub.4 OH ##STR216## " 280 " " " ##STR217## " 281 " ##STR218## " NHC.sub.2 H.sub.4 OCH.sub.3 " 282 " CH.sub.3 NHC.sub.2 H.sub.4 OCH.sub.3 NHC.sub.2 H.sub.4 C.sub.6 H.sub.4 SO.sub. 3 H orange 283 " CH.sub.3 NHC.sub.2 H.sub.4 C.sub.6 H.sub.4 SO.sub.3 H " " 284 " ##STR219## " " " 285 " CH.sub.2 C.sub.6 H.sub.4 SO.sub.3 H NHC.sub.2 H.sub.4 OCH.sub.3 NHC.sub.2 H.sub.4 OCH.sub.3 " 286 " " NHCH.sub.2 C.sub.6 H.sub.4 SO.sub.3 H NH(CH.sub.2).sub.3 OCH.sub.3 " 287 " N(C.sub.2 H.sub.5).sub.2 H NHC.sub.2 H.sub.4 C.sub.6 H.sub.4 SO.sub.3 H " 288 " " CH.sub.3 " " 289 " ##STR220## " NHC.sub.6 H.sub.4 SO.sub.3 H " 290 ##STR221## ##STR222## NHC.sub.2 H.sub.4 OH NHC.sub.2 H.sub.4 OH yellowish red 291 " N(C.sub.2 H.sub.5).sub.2 CH.sub.3 NHC.sub.2 H.sub.4 C.sub.6 H.sub.4 SO.sub.3 H orange 292 ##STR223## ##STR224## NHC.sub.2 H.sub.4 OH NHCH.sub.2 C.sub.6 H.sub.4 SO.sub.3 H yellowish red 293 ##STR225## " " " " 294 ##STR226## " " NHCH.sub.2 C.sub.6 H.sub.5 yellow 295 ##STR227## " " " " 296 ##STR228## " " " " 297 " " " ##STR229## " 298 " ##STR230## CH.sub.3 NHCH.sub.2 C.sub.6 H.sub.4 SO.sub.3 H " 299 ##STR231## ##STR232## NHC.sub.3 H.sub.7 NHC.sub.3 H.sub.7 " 300 " " NHC.sub.2 H.sub.4 OH NHC.sub.4 H.sub.9 " 301 " ##STR233## NH(CH.sub.2).sub.3 OH NH(CH.sub.2).sub.3 OC.sub.3 H.sub.7 (i) " 302 " CH.sub.3 " NHC.sub.2 H.sub.4 C.sub.6 H.sub.4 SO.sub.3 H " 303 " ##STR234## " NH(CH.sub.2).sub.3 OH " 304 " ##STR235## CH.sub.3 NHCH.sub.2 C.sub.6 H.sub.4 SO.sub.3 H " 305 ##STR236## ##STR237## NHC.sub.2 H.sub.4 OH NHC.sub.4 H.sub.9 " 306 " ##STR238## CH.sub.3 NHCH.sub.2 C.sub.6 H.sub.4 SO.sub.3 H " 307 ##STR239## ##STR240## NHC.sub.2 H.sub.4 OH NHC.sub.4 H.sub.9 orange 308 ##STR241## " " NHC.sub.2 H.sub.4 C.sub.6 H.sub.5 reddishorange 309 " " NH(CH.sub.2).sub.3 OCH.sub.3 NH(CH.sub.2).sub.3 OCH.sub.3 " 310 " N(C.sub.4 H.sub.9).sub.2 CH.sub.3 NHC.sub.2 H.sub.4 C.sub.6 H.sub.4 So.sub.3 H orange 311 ##STR242## ##STR243## NHC.sub.2 H.sub.4 OH NH(CH.sub.2).sub.3 OCH.sub.2 C.sub.6 H.sub.4 SO.sub.3 H " 312 " ##STR244## " " " 313 ##STR245## ##STR246## " NHC.sub.6 H.sub.13 red 314 " " " ##STR247## " 315 " ##STR248## " NHC.sub.2 H.sub.4 C.sub.6 H.sub.4 SO.sub.3 H " 316 " ##STR249## CH.sub.3 " reddishorange 317 " ##STR250## CH.sub.3 " " 318 ##STR251## ##STR252## NH(CH.sub.2).sub.3 OCH.sub.3 NH(CH.sub.2).sub.3 OCH.sub.3 yellowish red 319 " " NHC.sub.2 H.sub.4 OH NHC.sub.2 H.sub.4 OCH.sub.3 " 320 ##STR253## " " NHC.sub.2 H.sub.4 OH red
EXAMPLE 321
14.9 parts of the coupling product from 4-aminoazobenzene and 2-phenyl-4-.beta.-hydroxyethylamino-6-.beta.-methoxyethylaminopyrimidine is introduced while cooling into 200 parts of 96% sulfuric acid. The mixture is stirred for several hours at room temperature and then the solution is poured into an amount of ice-water enough to prevent the temperature rising above 10.degree. C. The precipitated dye of the probable formula: ##STR254## is filtered off, washed with water, dissolved in dilute caustic soda solution, filtered and precipitated as the sodium salt with sodium chloride. Conventional processing gives a reddish brown powder which colors synthetic polyamide material fast yellowish red hues.
EXAMPLE 322
A solution of 13.4 parts of the coupling product from 4-amino-2-methyl-5-methoxy-4'-.beta.-hydroxyethoxyazobenzene and 2-phenyl-4,6-bis-.gamma.-ethoxypropylaminopyrimidine in 150 parts of 96% sulfuric acid is stirred for twenty-four hours at room temperature. Then the mixture is added to so much ice that the temperature does not rise above 10.degree. C. The dye of the formula: ##STR255## is thus precipitated. It is isolated, dissolved in dilute caustic soda solution and reprecipitated as the sodium salt. At the end of processing a dark brown powder is obtained which gives full red hues having good fastnesses on polyamide cloth.
The dyes of the following Table are similarly prepare according to the methods expressly described in Example 1 to 4, 176 to 179 and 321 to 322:
Ex. No. DK X.sup.1 X.sup.2 X.sup.3 Hue 323 ##STR256## ##STR257## NH(CH.sub.2).sub.5 COOH NHC.sub.2 H.sub.4 OCH.sub.3 orange 324 ##STR258## " " " " 325 " " NHC.sub.2 H.sub.4 OCCC.sub.2 H.sub.4 COOH " " 326 ##STR259## " NHC.sub.2 H.sub.4 OH NHC.sub.2 H.sub.4 C.sub.6 H.sub.5 reddishyellow 327 " ##STR260## NH.sub.2 NHC.sub.2 H.sub.4 OH yellow 328 " " NHC.sub.2 H.sub.5 " reddish yellow 329 " ##STR261## CH.sub.3 NHC.sub.2 H.sub.4 OCH.sub.3 yellow 330 ##STR262## ##STR263## NHC.sub.2 H.sub.4 OSO.sub.3 H NH(CH.sub.2)OCH.sub.3 reddishyellow 331 ##STR264## ##STR265## NH(CH.sub.2).sub.5 COOH NHC.sub.2 H.sub.4 OCH.sub.3 reddishyellow 332 ##STR266## ##STR267## CH.sub.3 NH(CH.sub.2).sub.3 O(CH.sub.2).sub.4 OSO.sub.3 H orange 333 ##STR268## ##STR269## NHC.sub.2 H.sub.4 OSO.sub.3 H NHCH.sub.2 C.sub.6 H.sub.4 SO.sub.3 H yellow 334 " " NHC.sub.2 H.sub.4 SO.sub.3 H NH(CH.sub.2).sub.3 OCH.sub.3 " 335 " ##STR270## NHC.sub.2 H.sub.4 OH NHC.sub.6 H.sub.4 SO.sub.3 H " 336 " " NHC.sub.2 H.sub.4 OSO.sub.3 H NHC.sub.6 H.sub.5 " 337 " " " ##STR271## " 338 " ##STR272## NH(C.sub.2 H.sub.4 O).sub.2 SO.sub.3 H NH(C.sub.2 H.sub.4 O).sub.2 SO.sub.3 H " 339 ##STR273## ##STR274## NHC.sub.2 H.sub.4 OCOCH.sub.3 NH(CH.sub.2).sub.3 OCH.sub.3 " 340 ##STR275## ##STR276## NHC.sub.2 H.sub.4 OSO.sub.3 H NH(CH.sub.2).sub.3 OCH.sub.3 orange 341 " ##STR277## NHC.sub.2 H.sub.4 SO.sub.3 H " " 342 ##STR278## " NHC.sub.2 H.sub.4 OSO.sub.3 H NHC.sub.2 H.sub.4 OSO.sub.3 H " 343 " N(C.sub.2 H.sub.5).sub.2 CH.sub.3 NH(CH.sub.2).sub.3 OC.sub.2 H.sub.4 OC.sub.6 H.sub.4 SO.sub.3 H yellow 344 ##STR279## ##STR280## NHC.sub.2 H.sub.4 OSO.sub.3 H NHC.sub.2 H.sub.4 OSO.sub. 3 H " 345 ##STR281## " NHSO.sub.3 H NHC.sub.2 H.sub.4 OCH.sub.3 orange 346 " " NHC.sub.2 H.sub.4 SO.sub.3 H NH(CH.sub.2).sub.3 OCH.sub.3 reddish orange 347 " ##STR282## NHC.sub.2 H.sub.4 OSO.sub.3 H ##STR283## " 348 " " " ##STR284## " 349 " " NH(CH.sub.2).sub.6 OSO.sub.3 H NHC.sub.2 H.sub.4 OCH.sub.3 " 350 " N(C.sub.2 H.sub.5).sub.2 CH.sub.3 NHC.sub.2 H.sub.4 SO.sub.3 H " 351 ##STR285## ##STR286## NHC.sub.2 H.sub. 4 OSO.sub.3 H NHC.sub.2 H.sub.4 OSO.sub.3 H yellowishred 352 ##STR287## " " NHC.sub.4 H.sub.9 yellow 353 " ##STR288## NH(CH.sub.2).sub.3 OSO.sub.3 H NH(CH.sub.2).sub.3 OSO.sub.3 H " 354 ##STR289## ##STR290## NHC.sub.2 H.sub.4 OSO.sub.3 H NHC.sub.4 H.sub.9 " 355 ##STR291## " " " orange 356 ##STR292## " " NH(CH.sub.2).sub.3 OCH.sub.2 C.sub.6 H.sub.5 " 357 ##STR293## " NHC.sub.2 H.sub.4 SO.sub.3 H NH(CH.sub.2).sub.3 OCH.sub.3 red 358 ##STR294## " NHC.sub.2 H.sub.4 OCH.sub.3 NHC.sub.2 H.sub.4 OCH.sub.3 " 359 ##STR295## ##STR296## NH(CH.sub.2).sub.3 OH NH(CH.sub.2).sub.3 OH yellowishred 360 " ##STR297## " " " 361 " ##STR298## NHC.sub.2 H.sub.4 OH NHC.sub.2 H.sub.4 OH reddishorange 362 ##STR299## ##STR300## NH(CH.sub.2).sub.3 OCH.sub.3 NH(CH.sub.2).sub.3 OCH.sub.3violet 363 ##STR301## ##STR302## NHC.sub.2 H.sub.4 OHNHC.sub.2 H.sub.4 OH red 364 ##STR303## ##STR304## NHC.sub.2 H.sub.5 NHC.sub.2 H.sub.5 yellow 365 ##STR305## N(C.sub.2 H.sub.5).sub.2 CH.sub.3 NH(C.sub.2 H.sub.4 O).sub.2 H " 366 ##STR306## N(CH.sub.3).sub.2 CH.sub.3 NHC.sub.2 H.sub.4 C.sub.6 H.sub.5 " 367 ##STR307## N(C.sub.4 H.sub.9).sub.2 CH.sub.3 NHC.sub.2 H.sub.4 C.sub.6 H.sub.4 SO.sub.3 H " 368 ##STR308## ##STR309## CH.sub.3 NHC.sub.3 H.sub.6 OH " 369 ##STR310## ##STR311## NHC.sub.3 H.sub.6 OCH.sub.3 NHC.sub.3 H.sub.6 OCH.sub.3 " 370 ##STR312## ##STR313## NH(C.sub.2 H.sub.4 O).sub.2 H NH(C.sub.2 H.sub.4 O).sub.2 H " 371 ##STR314## N(C.sub.4 H.sub.9).sub.2 CH.sub.3 NHC.sub.2 H.sub.4 C.sub.6 H.sub.4 SO.sub.3 H " 372 ##STR315## ##STR316## NH.sub.2 NHC.sub.3 H.sub.6 OCH.sub.3 yellowishred 373 ##STR317## ##STR318## NH(C.sub.2 H.sub.4 O).sub.2 H NH(C.sub.2 H.sub.4 O).sub.2 H " 374 ##STR319## ##STR320## NH.sub.2 NHC.sub.3 H.sub.6 OCH.sub.3 " 375 ##STR321## N(C.sub.2 H.sub.5).sub.2 CH.sub.3 NHC.sub.2 H.sub.4 C.sub.6 H.sub.5 " 376 ##STR322## N(C.sub.3 H.sub.7).sub.2CH.sub.3 NHC.sub.6 H.sub.5 " 377 ##STR323## ##STR324## NHC.sub.2 H.sub.4 OCH.sub.3 NHC.sub.2 H.sub.4 OCH.sub.3 " 378 ##STR325## ##STR326## NH(C.sub.2 H.sub.4 O).sub.2 H NHC.sub.2 H.sub.4 C.sub.6 H.sub.4 SO.sub.3 H red 379 ##STR327## ##STR328## NHC.sub.2 H.sub.5 NHC.sub.2 H.sub.5 " 380 ##STR329## ##STR330## NHC.sub.3 H.sub.6 OH NHC.sub. 3 H.sub.6 OH " 381 ##STR331## ##STR332## NH(C.sub.2 H.sub.4 O).sub.2 H NH(C.sub.2 H.sub.4 O).sub.2 H " 382 ##STR333## ##STR334## NHC.sub.2 H.sub.4 OCH.sub.3 NHC.sub.2 H.sub.4 OCH.sub.3 " 383 ##STR335## ##STR336## NHC.sub.3 H.sub.6 OCH.sub.3 NHC.sub.3 H.sub.6 OCH.sub.3 " 384 ##STR337## ##STR338## NHC.sub.2 H.sub.5NHC.sub.2 H.sub.5 " 385 ##STR339## ##STR340## NHC.sub.3 H.sub.6 OH NHC.sub.3 H.sub.6 OH " 386 ##STR341## ##STR342## NH(C.sub.2 H.sub.4 O).sub.2 H NH(C.sub.2 H.sub.4 O).sub.2 H " 387 ##STR343## ##STR344## NHC.sub.6 H.sub.5NHC.sub.2 H.sub.4 OH orange 388 ##STR345## N(C.sub.2 H.sub.5).sub.2 CH.sub.3 ##STR346## yellow 389 ##STR347## ##STR348## CH.sub.3 NH(CH.sub.2).sub.3 O(CH.sub.2).sub.2 OC.sub.6 H.sub.4 SO.sub.3 H " 390 ##STR349## ##STR350## NHC.sub.2 H.sub.5 NHC.sub.2 H.sub.5 " 391 ##STR351## N(CH.sub.3).sub.2 CH.sub.3 ##STR352## " 392 " " " NHCH.sub.2 C.sub.6 H.sub.4 SO.sub.3 H " 393 " " " NH(CH.sub.2).sub.3 OCH.sub.2 C.sub.6 H.sub.4 SO.sub.3 H " 394 ##STR353## N(CH.sub.3).sub.2 CH.sub.3 ##STR354## " 395 ##STR355## ##STR356## NHCH.sub.2 C.sub.6 H.sub.4 SO.sub.3 H NHCH.sub.2 C.sub.6 H.sub.4 SO.sub.3 H " 396 " " NHC.sub.2 H.sub.4 C.sub.6 H.sub.4 SO.sub.3 H NHC.sub.2 H.sub.4 C.sub.6 H.sub.4 SO.sub.3 H " 397 ##STR357## " " " " 398 ##STR358## " " " yellowish red 399 ##STR359## " " " " 400 ##STR360## " " " red 401 " " NHCH.sub.2 C.sub.6 H.sub.4 SO.sub.3 H NHCH.sub.2 C.sub.6 H.sub.4 SO.sub.3 H " 402 ##STR361## " " " " 403 " " NH(C.sub.2 H.sub.4 O).sub.2 H NHC.sub.2 H.sub.4 C.sub.6 H.sub.4 SO.sub.3 H " 404 " " NHC.sub.2 H.sub.4 C.sub.6 H.sub.4 SO.sub.3 H " " 405 " " NH(CH.sub.2).sub.3 OCH.sub.2 C.sub.6 H.sub.4 SO.sub.3 H NH(CH.sub.2).sub.3 OCH.sub.2 C.sub.6 H.sub.4 SO.sub.3 H " 406 " " NH(CH.sub.2).sub.3 O(CH.sub.2).sub.2 OC.sub.6 H.sub.4 SO.sub.3 H NH(CH.sub.2).sub.3 O(CH.sub.2).sub.2 OC.sub.6 H.sub.4 SO.sub.3 H "
Claims
  • 1. A dye of the formula: ##STR362## in which D is selected from the group consisting of
  • (1) phenyl substituted by chloro; bromo; methyl; ethyl; trifluoromethyl; cyano; methylsulfonyl; ethylsulfonyl; phenylsulfonyl; C.sub.1 - to C.sub.4 -alkoxycarbonyl; carbamoyl; sulfamoyl; sulfamoyl substituted at the nitrogen once or twice by C.sub.1 - to C.sub.2 -alkyl, .beta.-hydroxyethyl, .gamma.-hydroxypropyl, .beta.-methoxyethyl or .gamma.-methoxypropyl; hydroxysulfonyl; SO.sub.2 NHC.sub.2 H.sub.4 SO.sub.3 H; or 6-methyl-7-sulfo-2-benzthiazolyl;
  • (2) phenylazophenyl;
  • (3) phenylazophenyl substituted by hydroxy, methyl, methoxy, ethoxy, hydroxysulfonyl or --OC.sub.2 H.sub.4 --O--SO.sub.3 H;
  • (4) 3- or 4-phthalimidyl; and
  • (5) 3- or 4-phthalimidyl substituted at the nitrogen by C.sub.1 - to C.sub.4 -alkyl, .beta.-hydroxyethyl, .beta.-methoxyethyl, .gamma.-hydroxypropyl, .beta.-hydroxyethoxyethyl, benzyl, phenylethyl, sulfobenzyl, sulfophenylethyl, phenyl or phenyl substituted by methyl or hydroxysulfonyl;
  • one Z is ##STR363## and the other Z is hydrogen; C.sub.1 - to C.sub.3 -alkyl; cyclohexyl; benzyl; sulfobenzyl; phenylethyl; sulfophenylethyl; phenyl; or phenyl substituted by methyl, chloro, methoxy, ethoxy or hydroxysulfonyl; Z.sup.1 is hydrogen; C.sub.1 - to C.sub.8 -alkyl; C.sub.2 - to C.sub.6 -alkyl substituted by hydroxy, methoxy, ethoxy or cyano; cyclohexyl; norbornyl; benzyl; sulfobenzyl; phenylethyl; sulfophenylethyl; phenylpropyl; sulfophenylpropyl; phenyl; phenyl substituted by methyl, methoxy, ethoxy, chloro or hydroxysulfonyl; sulfoethyl; (CH.sub.2).sub.3 OC.sub.6 H.sub.5 ; (CH.sub.2).sub.3 OC.sub.6 H.sub.4 SO.sub.3 H; (CH.sub.2).sub.3 OCH.sub.2 C.sub.6 H.sub.5 ; (CH.sub.2).sub.3 OCH.sub.2 C.sub.6 H.sub.4 SO.sub.3 H; C.sub.2 H.sub.4 OC.sub.2 H.sub.4 OH; (CH.sub.2).sub.3 OC.sub.2 H.sub.4 OZ.sup.5 ; or (CH.sub.2).sub.3 O(CH.sub.2).sub.4 OH;
  • Z.sup.3 has the meanings given for Z.sup.1 ;
  • Z.sup.2 is hydrogen or C.sub.1 - to C.sub.4 -alkyl;
  • Z.sup.1 and Z.sup.2 together with the nitrogen are pyrrolidino, piperidino or morpholino; and
  • Z.sup.5 is C.sub.1 - to C.sub.4 -alkyl, benzyl, sulfobenzyl, phenyl or sulfophenyl, with the proviso that the dye contains a total of 1, 2 or 3 sulfonic acid groups.
  • 2. A dye according to claim 1 having the formula ##STR364## in which Z is hydrogen; C.sub.1 - to C.sub.3 -alkyl; cyclohexyl; benzyl; sulfobenzyl; phenylethyl; sulfophenylethyl, phenyl; or phenyl substituted by methyl, chloro, methoxy, ethoxy or hydroxysulfonyl; and D, Z.sup.1 and Z.sup.3 have the meanings given for claim 1.
  • 3. A dye according to claim 1 having the formula ##STR365## in which Z is hydrogen; C.sub.1 - to C.sub.3 -alkyl; cyclohexyl; benzyl; sulfobenzyl; phenylethyl; sulfophenylethyl; phenyl; or phenyl substituted by methyl, chloro, methoxy, ethoxy or hydroxysulfonyl; and D, Z.sup.1, Z.sup.2 and Z.sup.3 have the meanings given for claim 1.
  • 4. A dye according to claim 1 having the formula ##STR366## in which D.sup.1 is a radical of the formula: ##STR367## p is zero or 1; Y is hydrogen, cyano, chloro, bromo, methylsulfonyl, ethylsulfonyl, phenylsulfonyl, methoxycarbonyl, ethoxycarbonyl or SO.sub.3 H;
  • Y.sup.1 is hydrogen, chloro, bromo or SO.sub.3 H;
  • Y.sup.2 is hydrogen, chloro, bromo, methyl, methylsulfonyl, methoxycarbonyl, ethoxycarbonyl, 6-methyl-7-sulfo-2-benzothiazolyl or SO.sub.3 H;
  • X is hydrogen, methyl, hydroxy, methoxy, ethoxy or SO.sub.3 H;
  • X.sup.1 is hydrogen, methyl or SO.sub.3 H;
  • X.sup.2 is hydrogen or methyl;
  • T is hydrogen, .beta.-hydroxyethyl, .gamma.-hydroxypropyl, .beta.-methoxyethyl, benzyl, phenyl or methylphenyl; and
  • Z and Z.sup.3 have the meanings given for claim 1.
  • 5. A dye according to the formula in claim 2 in which
  • Z is methyl, ethyl, propyl, benzyl, sulfobenzyl, phenyl or phenyl bearing methyl or methoxy,
  • Z.sup.1 is C.sub.1 to C.sub.4 -alkyl; C.sub.2 - or C.sub.3 -alkyl bearing hydroxy, methoxy or ethoxy as substituent; benzyl; sulfobenzyl; phenylethyl; sulfophenylethyl; phenylpropyl; sulfophenylpropyl; phenyl; phenyl bearing methyl, methoxy or hydroxysulfonyl as substituent; sulfoethyl; CH.sub.2 CH.sub.2 OCH.sub.2 --CH.sub.2 OH; (CH.sub.2).sub.3 O(CH.sub.2).sub.4 OH; (CH.sub.2).sub.3 OCH.sub.2 C.sub.6 H.sub.5 ; (CH.sub.2).sub.3 OCH.sub.2 C.sub.6 H.sub.4 SO.sub.3 H; (CH.sub.2).sub.3 O(CH.sub.2).sub.2 OC.sub.6 H.sub.5 ; or (CH.sub.2).sub.3 O(CH.sub.2).sub.2 OC.sub.6 H.sub.4 SO.sub.3 H;
  • Z.sup.3 is hydrogen or Z.sup.1 ; and
  • D has the meanings given for claim 2.
  • 6. A dye according to the formula in claim 3 in which
  • Z is methyl, ethyl, propyl or phenyl;
  • Z.sup.1 is C.sub.1 - to C.sub.4 -alkyl, cyclohexyl, benzyl, sulfobenzyl, phenylethyl or sulfophenylethyl;
  • Z.sup.2 is hydrogen or C.sub.1 - to C.sub.4 -alkyl;
  • Z.sup.1 and Z.sup.2 together with the nitrogen are pyrrolidino, piperidino or morpholino;
  • Z.sup.3 is C.sub.1 to C.sub.4 -alkyl; C.sub.2 - or C.sub.3 -alkyl bearing hydroxy, methoxy or ethoxy as substituent; benzyl; sulfobenzyl; phenylethyl; sulfophenylethyl; phenylpropyl, sulfophenylpropyl; phenyl; phenyl bearing methyl, methoxy or hydroxysulfonyl as substituent; sulfoethyl; CH.sub.2 CH.sub.2 OCH.sub.2 CH.sub.2 OH, (CH.sub.2).sub.3 OCH.sub.2 C.sub.6 H.sub.5, (CH.sub.2).sub.3 OCH.sub.2 C.sub.6 H.sub.4 SO.sub.3 H; (CH.sub.2).sub.3 O(CH.sub.2).sub.2 OC.sub.6 H.sub.5 ; (CH.sub.2).sub.3 O(CH.sub.2).sub.2 OC.sub.6 H.sub.4 SO.sub.3 H; or (CH.sub.2).sub.3 O(CH.sub.2).sub.4 OH; and D has the meanings given for claim 3.
  • 7. The dye according to claim 1 having the formula ##STR368##
  • 8. The dye according to claim 1 having the formula ##STR369##
  • 9. The dye according to claim 1 having the formula ##STR370##
  • 10. The dye according to claim 1 having the formula ##STR371##
  • 11. The dye according to claim 1 having the formula ##STR372##
  • 12. The dye according to claim 1 having the formula ##STR373##
Priority Claims (1)
Number Date Country Kind
2302582 Jan 1973 DEX
Parent Case Info

This application is a continuation-in-part of our copending application Ser. No. 434,248 (now abandoned).

US Referenced Citations (7)
Number Name Date Kind
3527748 Ackermann et al. Sep 1970
3531457 Ackermann et al. Sep 1970
3531458 Ackermann et al. Sep 1970
3532682 Ackermann et al. Oct 1970
3558261 Ackermann et al. Jan 1971
3598801 Beffa et al. Aug 1971
3856772 Dunkelmann et al. Dec 1974
Foreign Referenced Citations (1)
Number Date Country
2302582 Aug 1974 DEX
Non-Patent Literature Citations (1)
Entry
Venkataraman, "The Chemistry of Synthetic Dyes", vol. I, Academic Press Inc., New York, 1952, p. 270.
Continuation in Parts (1)
Number Date Country
Parent 434248 Jan 1974