Disperse dyes

Description

According to the invention there is provided a compound of the formula I ##STR3## in which D is a diazo component;
K is an aromatic group of the formula a, b or c ##STR4## where R is a group of the formula --CH(R.sub.4)--CO--O--R.sub.5, --CH.sub.2 CF.sub.3 or --CH.sub.2 CF.sub.2 CF.sub.2 H;
R.sub.6 is hydrogen or hydroxy,
R.sub.1 is hydrogen, chloro, C.sub.1-4 alkyl, C.sub.1-4 alkoxy or acylamino,
R.sub.2 is hydrogen, C.sub.1-4 alkoxy, C.sub.1-4 alkoxyethoxy, chloro, bromo and
R.sub.3 is selected from hydrogen, C.sub.1-6 alkyl, C.sub.3-4 alkenyl, chloroC.sub.3-4 alkenyl, bromoC.sub.3-4 alkenyl, C.sub.3-4 alkynyl, phenyl-C.sub.1-4 alkyl, C.sub.1-4 alkoxycarbonyl-C.sub.1-4 alkyl, C.sub.3-4 alkenyloxycarbonyl-C.sub.1-4 alkyl, C.sub.3-4 alkynyloxycarbonyl-C.sub.1-4 alkyl, phenoxy-C.sub.2-4 alkyl, --CH.sub.2 --CH(R.sub.8)CH.sub.2 --R.sub.9 and C.sub.2-4 alkyl substituted by 1 to 3 groups selected from halogen, cyano, C.sub.1-4 alkoxy, C.sub.1-4 alkylcarbonyloxy and C.sub.1-4 alkoxycarbonyloxy;
or R.sub.2 together with R.sub.3 in the group a) form a group of the formula-*CH(CH.sub.3)CH.sub.2 C(CH.sub.3).sub.2 where the * carbon atom is attached to the group a);
R.sub.4 is hydrogen, phenyl or C.sub.1-4 alkyl,
R.sub.5 is phenyl, unsubstituted or substituted by one to three groups selected from halogen (preferably Cl or Br) C.sub.1-4 alkyl, C.sub.1-4 alkoxycarbonyl and C.sub.1-4 alkoxy or phenyl substituted by one group selected from formyl, cyan, rhodan, phenyl, benzyloxy, C.sub.1-4 alkoxycarbonyl-C.sub.1-2 alkoxy, C.sub.1-4 alkylcarbonylamino, C.sub.1-4 alkylcarbonyloxy and nitro;
or R.sub.5 is alpha or beta naphthyl, phenyl-C.sub.1-4 alkyl or 1-phenyl-propenyl-3, in which the phenyl group (in phenyl C.sub.1-4 alkyl and 1-phenyl propenyl-3) is unsubstituted or substituted by one or two substituents selected from halogen, C.sub.1-4 alkyl and C.sub.1-4 alkoxy or by one nitro or C.sub.1-4 alkoxycarbonyl group; or
R.sub.5 is allyl, haloallyl, methallyl, propargyl, tetrahydrofuryl-2-methyl, tetrahydropyranyl-2-methyl, chlor-C.sub.2-4 alkyl, bromoC.sub.2-4 alkyl or a group of the formula ##STR5## R.sub.7 is hydrogen or C.sub.1-4 alkyl; R.sub.8 is hydroxy, C.sub.1-4 alkylcarbonyloxy or C.sub.1-4 alkoxycarbonyloxy;
R.sub.9 is chloro, C.sub.1-4 alkoxy, phenoxy, allyloxy or C.sub.1-4 alkylcarbonyloxy;
R.sub.10 is hydrogen or C.sub.1-4 alkyl;
R.sub.11 is hydrogen, halogen (preferably chloro or bromo), C.sub.1-4 alkyl, C.sub.1-4 alkoxy or nitro
Y is C.sub.2-3 alkylene and
n is 0 or 1;
with the proviso that when K is a group of formula b) or c), then R.sub.3 is hydrogen.
Preferred diazo components D are single or fused carbocyclic or heterocyclic aromatic amines which may bear any of the usual substituents for disperse dyes, preferably excluding water solubilising groups, especially sulpho groups. Examples of such diazo components contain a phenyl, thienyl, thiazolyl, isothiazolyl, thiadiazolyl, pyrazolyl, imidazolyl, triazolyl, benzthiazolyl or benzisothiazolyl group. The compounds of formula I are preferably monoazo compounds.
The aromatic or heteroaromatic rings can bear one to three groups selected from the following: --COOC.sub.1-8 alkyl, halogen (e.g. Cl, Br and I), nitro,cyano, rhodan, C.sub.1-4 alkyl, C.sub.1-4 alkoxy, phenyl and phenoxy and especially on any thienyl or thiazolyl diazo component additionally formyl, --CH.dbd.CH--NO.sub.2, --CH.dbd.C(CN).sub.2 and --CH.dbd.C(CN)--CO--C.sub.1-8 alkyl.
Preferred acyl groups include R.sub.40 --Z-- in which
R.sub.40 is a C.sub.1-8 alkyl or phenyl group that may bear one to three groups selected from the following: halogen (e.g. Cl, Br and I), nitro, cyano, rhodan, hydroxy, C.sub.1-4 alkyl, C.sub.1-4 alkoxy, phenyl, C.sub.1-4 alkoxycarbonyl and phenoxy groups;
Z is a radical --CO-- --O--CO--, --CO--O--, --SO.sub.2 -- and --SO.sub.2 --N(R.sub.7); where * atom is attached to R.sub.40 and R.sub.7 is as defined above;
Preferred acylamino groups are --NH--Z.sub.1 --R.sub.40, where Z.sub.1 is --CO--; ##STR6## and In this Specification, any phenyl is unsubstituted or substituted by one or two groups selected from chloro, methyl, ethyl and C.sub.1-2 alkoxy or one group nitro.
In Y preferably the alkylene group is a group of the formula --CH.sub.2 CH.sub.2 --, --CH.sub.2 --CH(CH.sub.3)--, more preferably --CH.sub.2 CH.sub.2 --
Preferably R.sub.40 is R.sub.40 ' where R.sub.40 ' is a C.sub.1-4 alkyl group or phenyl.
Preferably D is D.sub.1 where D.sub.1 is a compound of formula 1 to 11 below ##STR7## in which R.sub.20 is hydrogen, chloro, bromo, cyano, nitro-, C.sub.1-4 alkoxy carbonyl, C.sub.1-4 alkylsulphonyl (preferably hydrogen, cyano, chloro or nitro);
R.sub.21 is chloro, bromo, nitro, C.sub.1-4 alkyl, C.sub.1-4 alkylsulfonyl, C.sub.1-4 alkylcarbonyl, aminosulfonyl, mono- or di-C.sub.1-4 alkylaminosulfonyl, phenylaminosulfonyl, C.sub.1-4 alkoxycarbonyl, aminocarbonyl, mono- or di-C.sub.1-4 -alkylaminocarbonyl, phenylaminocarbonyl, phenylazo, benzyloxycarbonyl, tetrahydrofurfuryl-2-oxycarbonyl, C.sub.3-4 alkenyloxycarbonyl oder C.sub.3-4 alkinyloxycarbonyl;
R.sub.22 is hydrogen, chloro, bromo or cyano;
R.sub.23 is hydrogen or chloro, or when R.sub.22 is hydrogen, R.sub.23 is additionally rhodan;
R.sub.24 is nitro, C.sub.1-4 alkylcarbonyl, C.sub.1-4 alkoxycarbonyl, cyano, aminocarbonyl, mono- or di-C.sub.1-2 alkylaminocarbonyl;
R.sub.25 is hydrogen, chloro, bromo, C.sub.1-4 alkyl or phenyl;
R.sub.26 is nitro, cyano, formyl, dicyanovinyl or a group of the formula --CH.dbd.CH--NO.sub.2, --CH.dbd.C(CN)CO--OC.sub.1-4 -alkyl, H.sub.5 C.sub.6 --N.dbd.N-- or 3- or 4--NO.sub.2 --C.sub.6 H.sub.4 --N.dbd.N--;
R.sub.27 is cyano or C.sub.1-4 alkoxycarbonyl;
R.sub.28 is C.sub.1-4 alkyl or phenyl;
R.sub.29 is --CN, --CH.dbd.CH.sub.2 or phenyl;
R.sub.30 is C.sub.1-4 alkyl;
R.sub.31 is hydrogen chlor, bromo, cyano, rhodan, nitro, C.sub.1-4 alkoxycarbonyl or di-C.sub.1-4 alkylaminosulfonyl;
R.sub.32 is hydrogen, chloro, or bromo; and
R.sub.33 is C.sub.1-4 alkyl, C.sub.1-4 alkylcarbonyl-C.sub.1-4 alkylene or --C.sub.1-4 alkylene-COOCH.sub.2 CF.sub.3
in which any phenyl group present in R.sub.20 to R.sub.30 is unsubstituted or substituted by one or two groups selected from chloro, bromo, methyl, ethyl, methoxy and ethoxy.
Preferably K is K.sub.1 where K.sub.1 is a group of formula a) defined above.
Preferably R is R' where R' is --CH(R.sub.4 ')--CO--O--R.sub.5 ' or CH.sub.2 CF.sub.3 where R.sub.4 ' and R.sub.5 ' are defined below.
Preferably R.sub.1 is R.sub.1 ' where R.sub.1 ' is selected from hydrogen, C.sub.1-2 alkyl, chloro and acylamino,
Preferably R.sub.2 is R.sub.2 ' where R.sub.2 ' is selected from hydrogen, chloro, C.sub.1-2 alkoxy, C.sub.1-2 alkoxyethoxy or R.sub.2 ' (when in formula a) together with R.sub.3 forms the group --CH(CH.sub.3)CH.sub.2 C(CH.sub.3).sub.2.
Preferably R.sub.3 is R.sub.3 ' where R.sub.3 ' is selected from hydrogen, C.sub.1-4 alkyl, cyanoethyl, C.sub.1-2 alkoxyethyl, C.sub.3-4 alkenyl, chloroallyl, C.sub.3-4 alkynyl, C.sub.1-2 alkoxycarbonylmethyl, allyloxycarbonylmethyl or propargyloxycarbonylmethyl.
Preferably R.sub.4 is R.sub.4 ' where R.sub.4 ' is selected from hydrogen and C.sub.1-2 alkyl.
Preferably R.sub.5 is R.sub.5 ' where R.sub.5 ' is phenyl, unsubstituted or substituted by one or two substituents selected from chloro, C.sub.1-2 alkyl, C.sub.1-2 alkoxy and one phenyl; phenoxy ethyl; phenyl C.sub.1-2 alkyl; or 1-phenylpropenyl-3-, the phenyl group of each of the last three substituents (phenyl C.sub.1-2 alkyl, phenoxy ethyl or 1-phenylpropenyl-3-) being unsubstituted or substituted by one or two groups selected from chloro, methyl and C.sub.1-2 alkoxy or one group nitro) or R.sub.5 ' is alpha and beta naphthyl.
Preferably Y is Y' where Y' is a group of the formula --CH.sub.2 CH.sub.2 -- or --CH.sub.2 CH(CH.sub.3)--.
More preferably R is R" where R" is is --CH(R.sub.4 ')--CO--O--R.sub.5 ' where R.sub.4 ' is selected from hydrogen and C.sub.1-2 alkyl and where R.sub.5 ' is phenyl, unsubstituted or substituted by one or two substituents selected from chloro, C.sub.1-2 alkyl, C.sub.1-2 alkoxy and one phenyl; phenyl C.sub.1-2 alkyl, phenoxy ethyl or 1-phenylpropenyl-3 (the phenyl group of each of the last three substituents phenyl C.sub.1-2 alkyl, phenoxy ethyl or 1-phenylpropenyl-3) being unsubstituted or substituted by one or two groups selected from chloro, methyl and C.sub.1-2 alkoxy or one group nitro or R.sub.5 ' is alpha and beta naphthyl.
More preferably R.sub.3 is R.sub.3 " where R.sub.3 " is C.sub.1-4 alkyl or cyanoethyl.
More preferably R.sub.5 is R.sub.5 " where R.sub.5 " is phenyl, phenoxyethyl or benzyl, in which the phenyl group of each substituent is unsubstituted or substituted by one or two groups selected from chloro, methyl and C.sub.1-2 alkoxy or one nitro group.
More preferably Y is Y" where Y" is 1,2 ethylene.
More preferably D is D.sub.2 where D.sub.2 is a diazo component of the 2,6-dicyano-4-chlorophenyl, 2,6-dicyano-4-bromo-phenyl, 2,6-dicyano-4-methylphenyl, 2,6-dicyano-4-nitrophenyl; 2,4-dinitro-6-chlorophenyl, 2,4-dinitro-6-bromophenyl, 2,4-dinitro-6-cyanophenyl, 2-chloro- or 2-bromo-4-nitro-6-cyanophenyl, 2,4-dinitrophenyl, 2,6-dichloro- or 2,6-dibromo-4-nitrophenyl, 2-chloro-4-nitro-6-bromophenyl, 2-chloro- or 2-cyano-4-nitrophenyl, 2,4-dinitro-5-chlorophenyl, 2,4-dinitro-5,6-dichlorophenyl, 2,5-dichloro-4-nitro-phenyl, 4-nitrophenyl, 4-phenylazophenyl, 4-C.sub.1-4 alkoxycarbonyl-phenyl, 2-C.sub.1-4 alkoxycarbonyl-4-nitrophenyl, 4-benzyloxycarbonylphenyl, 4-(tetrahydrofurfuryl-2'-oxycarbonyl)-phenyl, 3,5-dicyano-4-chlorothienyl-2,3,5-dicyanothienyl-2,3-cyano-5-nitro-thienyl-2,3-acetyl-5-nitrothienyl-2,3,5-dinitrothienyl-2,3-(C.sub.1-4 alkoxycarbonyl)-5-nitrothienyl-2,5-phenylazo-3-cyanothienyl-2,5-phenylazo-3-cyano-4-methyl-thienyl-2,5-nitrothiazolyl-2,5-nitro-benzisothiazolyl-3,3-methyl-4-cyano-isothiazolyl-5,3-Phenyl-1,2,4-thiadiazolyl-2,5-(C.sub.1-2 alkylmercapto)-1,3,4-thiadiazolyl-2,3-C.sub.1-4 alkoxycarbonylethylmercapto-1,2,4-thiadiazolyl-5,1-cyanomethyl-4,5-dicyano-imidazolyl-2,6-nitrobenzthiazolyl-2,5-nitrobenzthiazolyl-2,6 -rhodan-benzthiazolyl-2,6-chlorobenzthiazolyl-2,(5),6,(7)-dichlorobenzthiazolyl-2, or a group of the formula ##STR8## where R.sub.35 is oxygen or a group of the formula ##STR9##
Most preferably R is R'" where R'" is a group of the formula --CH.sub.2 CO--O--R.sub.5 ", where R.sub.5 " is defined above.
Preferred compounds of formula I are of formula Ia ##STR10## in which the symbols D.sub.1, R.sub.1 ', R.sub.2 ', R.sub.3, Y', R.sub.4 ' and R.sub.5 are as defined above.
In a compound of formula Ia preferably D.sub.1 is D.sub.2 defined above, more preferably D.sub.1 is D.sub.3 where D.sub.3 is a diazo component of the 2,4-dinitro-6-chlorophenyl, 2,4-dinitro-6-bromophenyl, 2,4-dinitro-6-cyanophenyl, 2,4-dinitro-5-chlorophenyl, 2,4-dinitro-5-rhodan-phenyl, or 2,4-di-nitro-5,6-dichlorophenyl series.
Most preferably D.sub.1 is D.sub.3 ' where D.sub.3 ' is a diazo component of the 2,4-dinitro-6-chlorophenyl or 2,4-dinitro-6-bromophenyl series.
More preferred compounds of formula I are of formula Ib ##STR11## in which the symbols D.sub.2, R.sub.1 ', R.sub.2 ', R.sub.3, Y', R.sub.4 ' and R.sub.5 are as defined above.
Preferred compounds of formula I b are those in which R.sub.1 ' is R.sub.1 " and R.sub.2 ' is R.sub.2 ".
Alternatively preferred compounds of formula I are those of formula Ic ##STR12## in which D.sub.3 is as defined above; R' is --CH(R.sub.4 ')--CO--O--R.sub.5 ' or --CO--O--CH.sub.2 CF.sub.3 where R.sub.4 ' and R.sub.5 ' are defined below;
R.sub.1 " is acylamino. (Preferably the acyl groups of acylamino are selected from R.sub.40 --Z-- defined above, especially NH--COC.sub.1-4 alkyl);
R.sub.2 " is C.sub.1-2 alkoxy or C.sub.1-2 alkoxyethoxy,
R.sub.3 ' is selected from hydrogen, C.sub.1-2 alkoxyethyl, C.sub.3-4 alkenyl, chloro-C.sub.3-4 alkenyl, C.sub.3-4 alkynyl, C.sub.1-2 alkoxy-carbonylmethyl, allyloxycarbonylmethyl or propargyl-oxycarbonylmethyl;
R.sub.4 ' is selected from hydrogen and C.sub.1-2 alkyl;
R.sub.5 ' is phenyl, unsubstituted or substituted by one or two substituents selected from chloro, C.sub.1-2 alkyl, C.sub.1-2 alkoxy and phenyl; phenyl C.sub.1-2 alkyl, phenoxy ethyl or 1-phenylpropenyl-3, (the phenyl group of each of the last three substituents (phenyl C.sub.1-2 alkyl, phenoxy ethyl or 1-phenylpropenyl-3) being unsubstituted or substituted by one or two groups selected from chloro, methyl and C.sub.1-2 alkoxy or one group nitro) or R.sub.5 ' is alpha and beta naphthyl; and
is a group of the formula --CH.sub.2 CH.sub.2 -- or --CH.sub.2 CH(CH.sub.3)--.
Alternatively preferred compounds of formula Ic are those in which
D.sub.3 is D.sub.3 ' where D.sub.3 ' is a diazo component of the 2,4-dinitro-6-chlorophenyl or 2,4-dinitro-6bromophenyl series;
R' is R'" where R'" is a group of the formula --CH.sub.2 CO--O--R.sub.5 ", where R.sub.5 " is defined below;
R.sub.1 " is --NH--COC.sub.1-2 alkyl;
R.sub.2 " is R.sub.2 '" where R.sub.2 '" is C.sub.1-2 alkoxy;
R.sub.3 ' is R.sub.3a where R.sub.3a is hydrogen, allyl, chloroallyl or propargyl;
R.sub.5 ' is R.sub.5 " where R.sub.5 " is phenyl, phenoxyethyl or benzyl, in which the phenyl group of each substituent is unsubstituted or substituted by one or two groups selected from chloro, methyl and C.sub.1-2 alkoxy or one group nitro; and
Y' is Y" where Y" is 1,2 ethylene.
Further alternative preferred compounds of formula I are those of formula Id ##STR13## in which D.sub.4 is a diazo component of the 4-nitrophenyl, 2-chloro-4-nitrophenyl, 2,6-dichloro-4-nitrophenyl, 2-chloro-4-nitro-6-bromophenyl or 2-cyano-4-nitrophenyl series.
R.sub.1a is hydrogen, methyl, acylamino or chloro;
R.sub.b is a group of the formula --CH(R.sub.4 ')--CO--O--R.sub.5 ', where R.sub.4 ' where R.sub.4 ' is selected from hydrogen and C.sub.1-2 alkyl and R.sub.5 ' is phenyl, unsubstituted or substituted by one or two substituents selected from chloro, C.sub.1-2 alkyl, C.sub.1-2 alkoxy and phenyl; phenyl C.sub.1-2 alkyl, phenoxy ethyl or 1-phenylpropenyl-3 (the phenyl group of each of the last three substituents (phenyl C.sub.1-2 alkyl, phenoxy ethyl or 1-phenylpropenyl-3) being unsubstituted or substituted by one or two groups selected from chloro, methyl and C.sub.1-2 alkoxy or one group nitro or R.sub.5 ' is alpha and beta naphthyl;
R.sub.3b is C.sub.1-4 alkyl, cyano-C.sub.2-4 alkyl, C.sub.1-4 alkoxyethyl, --C.sub.2 H.sub.4 --O--CO--C.sub.1-4 alkyl, --C.sub.2 H.sub.4 --O--CO--OC.sub.1-4 alkyl or benzyl; and
Y is Y' where Y' is a group of the formula --CH.sub.2 CH.sub.2 -- or --CH.sub.2 CH(CH.sub.3)--.
Preferred compounds of formula Id are those in which D.sub.4 is D.sub.5 where D.sub.5 is 2,6-dichloro-4-nitrophenyl or 2-cyano-4-nitrophenyl, R.sub.1a is hydrogen, R.sub.3b is C.sub.1-4 alkyl, R.sub.4 ' is hydrogen and Y' is --CH.sub.2 CH.sub.2 --.
The compounds of formula I can be prepared by known methods from known compounds. For example the compounds of formula I can be prepared by coupling one mole of a diazotised amine of formula II
D--NH.sub.2 (II)
with one mole of a compound of formula III
H--K--N(R.sub.3)--Y--CO--OR (III).
Diazotisation and coupling can be carried out by known methods.
The compounds of formula II and III are known or can be made from known compounds by known methods.
The new compounds of formula I exhaust well from aqueous medium onto textile material based on synthetic or semisynthetic, hydrophobic, high molecular weight organic material. In particular the compounds of formula I are useful for dyeing or printing textile material made from linear aromatic polyester, cellulose 21/2 acetate and cellulose triacetate. Linear aromatic polyester also include polyester microfibers (ref. Chemie Fasern Industrie, 43 (4) E. 34-36 (1993))
Dyeing and printing can be carried out by known methods, for example as exemplified in French Patent 1,445,371 (GB Patent 1,114,433).
The compounds of the invention have good all round fastness properties, in particular good thermomigration properties, good lightfastness, good thermofixation, good blistering properties as well as good wet fastness properties, especially after thermal fixation (in particular in the M&S C4A household wash test). Worthy of mention is also the suitability of the compounds of formula I for Thermo-Transfer printing.

The invention will be further illustrated by the following Examples in which all parts and percentages are by weight.
EXAMPLE 1
16.3 parts of 2-amino-5-nitrobenzonitrile are stirred into 100 parts of 93% cold sulphuric acid and are then reacted, over 30 minutes with 32 parts of 40% nitrosylsulphuric acid at 0.degree.-5.degree. C.
This is stirred for 3 to 4 hours at 0.degree. to 5.degree. C. and the resultant diazonium solution is poured, whilst stirring well onto a mixture of 35.7 parts of 3-(N-methyl-N-phenylamino)propionic acid-(2'-phenoxyethoxycarbonylmethyl ester), 100 parts of glacial acetic acid, 2 parts of amidosulphonic acid, 200 parts of water and 500 parts of ice.
The resultant precipitated dyestuff is filtered, washed salt free with water and dried under vacuum at 60.degree. C. The resulting dyestuff is of the formula 1a ##STR14##
This dyestuff can dye polyester material a rubin red colour and has excellent properties, especially good wet fastness properties after thermofixation. This dyestuff is particularly suited for modern Rapid Dyeing processes.
.lambda.max=529 nm (DMF).
EXAMPLE 2
Example 1 is repeated using instead of 35.7 parts of 3-(N-methyl-N-phenylamino)propionic acid-(2'-phenoxyethoxycarbonylmethyl ester), 37.1 parts of 3-(N-ethyl-N-phenylamino)propionic acid (2'-phenoxyethoxycarbonylmethyl ester). The resultant dyestuff is of the formula 2a ##STR15##
This dyestuff dyes polyester a red tone and produces good fastness properties, in particular good wet fastness properties after thermofixation.
.lambda.max=534 nm.(DMF)
EXAMPLE 3
Example 1 is repeated using instead of 35.7 parts of 3(N-methyl-N-phenylamino)propionic acid-(2'-phenoxyethoxycarbonylmethyl ester), 42.9 parts of 3-(N-2'-acetoxyethyl-N-phenylamino) propionic acid (2"-phenoxyethoxycarbonylmethyl ester).
The resultant dyestuff is of the formula 3a ##STR16##
This dyestuff dyes polyester a red tone and produces good fastness properties, in particular good wet fastness properties after thermofixation.
.lambda.max=523 nm. (DMF).
EXAMPLE 4
20.7 parts of 1-amino-2,6-dichloro-4-nitrobenzene are stirred into 100 parts of 93% sulphuric acid and then are reacted at 30.degree. C. over 1 hour with 32 parts of 40% nitrosylsulphuric acid. This mixture is stirred a further 2 to 3 hours at this temperature and the resulting diazonium salt solution is added whilst slowly stirring to a mixture of 35,7 parts of 3-(N-methyl-N-phenylamino)-propionic acid-(2'-phenoxyethoxycarbonylmethyl ester), 100 parts of glacial acetic acid, 2 parts of amidosulphonic acid, 200 parts of water and 500 parts of ice.
The resultant precipitated dyestuff is filtered, washed salt free with water and dried under vacuum at 60.degree. C. The resulting dyestuff is of the formula 4a ##STR17##
This dyestuff can dye polyester material a yellow brown tone with good fastness properties, in particular, good wet fastness properties after thermal fixation.
.lambda. max (DMF)=439 nm.
EXAMPLE 5
21.8 parts of 2-chloro-4,6-dinitroaniline are stirred into 150 parts of 93% sulphuric acid at 15.degree.-20.degree. C. and this is then reacted over 30 minutes with 32 parts of 40% nitrosylsulphuric acid. This is stirred for 2-3 hours and the resultant diazonium salt solution is slowly poured whilst stirring onto a mixture of 46.8 parts of 3-[N-propargyl-N-(5"-acetylamino-2"-methoxy-phenylamino)]-propionic acid-(2'-phenoxyethoxycarbonylmethyl ester), 100 parts of glacial acetic acid, 2 parts of amidosulphonic acid, 200 parts of water and 500 parts of ice.
The resultant precipitated dyestuff is filtered, washed salt free with water and dried under vacuum at 60.degree. C. The resulting dyestuff is of the formula 5a ##STR18##
This dyestuff can dye polyester material a navy blue colour and has excellent fastness properties, especially fastness properties
EXAMPLE 6
21.8 parts of 2-chloro-4,6-dinitroaniline are stirred into 150 parts of 93% sulphuric acid at 15.degree.-20.degree. C. and this is then reacted over 30 minutes with 32 parts of 40% nitrosylsulphuric acid. This is stirred for 2-3 hours in an ice bath and the resultant diazonium salt solution is slowly poured continuously, whilst stirring onto a mixture of 48,5 parts of 3-(N-allyl-N-(5"-acetylamino-2"-methoxyphenylamino))-propionic acid-(4'-nitro-benzyloxycarbonylmethyl ester), 100 parts of glacial acetic acid, 2 parts of amidosulphonic acid and 300 parts of ice.
The resultant precipitated dyestuff is filtered, washed salt free with water and dried under vacuum at 60.degree. C. The resulting dyestuff is of the formula 6a ##STR19##
This dyestuff can dye polyester material a navy blue colour and has excellent fastness properties, especially wet fastness properties after thermofixation.
.lambda. max (DMF)=597 nm.
EXAMPLE 7
21.8 parts of 2-chloro-4,6-dinitroaniline are stirred into 150 parts of 93% sulphuric acid at 15.degree.-20.degree. C. and this is then reacted over 30 minutes with 32 parts of 40% nitrosylsulphuric acid. This is stirred for 2-3 hours in an ice bath and the resultant diazonium salt solution is slowly poured continuously, whilst stirring onto a mixture of 40 parts of 3-N-(5"-acetylamino-2"-methoxyphenylamino)-propionic acid-(benzyloxycarbonylmethyl ester), 100 parts of glacial acetic acid, and 300 parts of ice/water.
The resultant precipitated dyestuff is filtered, washed salt free with water and dried under vacuum at 60.degree. C.
The resulting dyestuff is of the formula 7a ##STR20##
This dyestuff can dye polyester material and polyester/cotton mixed fabrics a navy blue colour and has excellent fastness properties, especially wet fastness properties after thermofixation.
.lambda. max (DMF)=595 nm.
EXAMPLE 8
21.8 parts of 2-chloro-4,6-dinitroaniline are stirred into 150 parts of 93% sulphuric acid at 15.degree.-20.degree. C. and this is then reacted over 30 minutes with 32 parts of 40% nitrosylsulphuric acid. This is stirred for 2-3 hours in an ice bath and the resultant diazonium salt solution is slowly poured continuously, whilst stirring onto a mixture of 44.5 parts of 3-[N-allyl-N-(5"-acetylamino-2"-methoxyphenylamino)]-propionic acid-(2'-methyl-phenoxycarbonylmethyl)-ester, 100 parts of glacial acetic acid, 2 parts of amidosulphonic acid and 300 parts of ice.
The resultant precipitated dyestuff is filtered, washed salt free with water and dried under vacuum at 60.degree. C. The resulting dyestuff is of the formula 8a ##STR21##
This dyestuff can dye polyester fibre material a navy blue colour and has excellent fastness properties, especially good wet fastness properties after thermofixation.
.lambda. max (DMF)=597 nm.
The compound of formula 8a is particularly suitable for use alone or in a navy blue or black mixture and is particularly suitable for use in rapid dyeing, especially the Foron (registered trademark) RD process.
EXAMPLE 9
16.3 parts of 2-amino-5-nitrobenzonitrile are stirred into 150 parts of 93% sulphuric acid at 15.degree.-0.degree. C. and this is then reacted over 30 minutes at 0 to 5 with 32 parts of 40% nitrosylsulphuric acid. This is stirred for 2-3 hours in an ice bath and the resultant diazonium salt solution is slowly poured continuously, whilst stirring onto a mixture of 34.2 parts of 3-(N-methyl-N-phenylamino)-propionic acid-3',5'-dimethylphenoxycarbonylmethyl ester, 100 parts of glacial acetic acid, 2 parts of amidosulphonic acid and 500 parts of ice/water.
The resultant precipitated dyestuff is filtered, washed salt free with water and dried under vacuum at 60.degree. C. The resulting dyestuff is of the formula 9a ##STR22##
This dyestuff can dye polyester fibre material a rubin colour and has excellent fastness properties
.lambda. max (DMF)=532 nm.
The compound of formula 9a is particularly suitable for use alone or in mixture and is particularly suitable for use in rapid dyeing, especially the Foron (registered trademark) RD process. The wet fastness properties are good.
EXAMPLE 10
18.6 parts of 2-amino-4-chloro-3-cyano-5-formyl-thiophene are dissolved in 200 parts of 85% sulphuric acid. Whilst stirring, 33 parts of 40% nitrosyl sulphuric acid are added and stirred for about 3 hours at about 0.degree. C. The resulting brown diazonium salt solution is added whilst stirring well, to a solution of 18 parts of 3-(N-ethyl-N-3"-methylphenylamino)-propionic acid-2'- and 4') respectively) methylphenoxycarbonylmethyl ester and 2 parts of amidosulphonic acid in 50 parts of 5% sulphuric acid. The coupling temperature is maintained by external cooling any by the addition of 200 parts of ice. The dyestuff suspension is stirred for 1 to 2 hours, filtered and washed acid free with 300 parts of water. The product is dried under vacuum at 50.degree. C. An isomeric dyestuff mixture of the formula 10a ##STR23## results.
This mixture dyes polyester a brilliant reddish blue tone with good fastness properties. The .lambda. max. (DMF)=610 nm
EXAMPLE 11
21.8 parts of 2-chloro-4,6-dinitroaniline are stirred into 150 parts of 93% sulphuric acid at 15.degree.-20.degree. C. and then this is reacted at 30.degree. C. over 1 hour with 32 parts of 40% nitrosylsulphuric acid. This mixture is stirred a further 2 to 3 hours at this temperature and the resulting diazonium salt solution is added whilst slowly stirring to a mixture of 44.5 parts of 3-(N-(5"-acetylamino-2"-methoxyphenylamino))-propionic acid-n-(4-nitro-benzyloxy-carbonylmethyl ester), 100 parts of glacial acetic acid, 2 parts of amidosulphonic acid and 300 parts of ice.
The resultant precipitated dyestuff is filtered, washed salt free with water and dried under vacuum at 60.degree. C. The resulting dyestuff is of the formula 11a ##STR24##
This dyestuff can dye polyester fibre material a navy blue colour and has excellent fastness properties, especially good wet fastness properties after thermofixation.
.lambda. max (DMF)=595 nm.
The compound of formula 11a is particularly suitable for use alone or in a navy blue or black mixture and is particularly suitable for use in rapid dyeing, especially the Foron (registered trademark) RD process.
EXAMPLE 12
16.3 parts of 2-amino-5-nitrobenzonitrile are stirred into 100 parts of 93% cold sulphuric acid and are then reacted, over 30 minutes with 32 parts of 40% nitrosylsulphuric acid at 0.degree.-5.degree. C.
This is stirred for 3 to 4 hours at 0.degree. to 5.degree. C. and the resultant diazonium solution is poured, whilst stirring well onto a mixture of 40.1 parts of 3-(N-methyl-N-phenylamino)propionic acid-(2"-phenoxyethoxy-2'-ethoxy-carbonylmethyl ester), 100 parts of glacial acetic acid, 2 parts of amidosulphonic acid, 200 parts of water and 500 parts of ice.
The resultant precipitated dyestuff is filtered, washed salt free with water and dried under vacuum at 60.degree. C. The resulting dyestuff is of the formula 12a ##STR25##
This dyestuff can dye polyester material a rubin red colour and has excellent fastness properties, especially good wet fastness properties after thermofixation. This dyestuff is particularly suited for modern Rapid Dyeing processes.
.lambda.max=531 nm (DMF).
EXAMPLES 13-433
The compounds of Tables 1 to 17 can be synthesised from known products analogously to an appropriate method according to Example 1-12.
TABLE 1__________________________________________________________________________ ##STR26##Ex. NuanceNo. R.sub.6 R.sub.7 R.sub.2 R.sub.1 R.sub.3 R.sub.5 on PES__________________________________________________________________________13 Cl NO.sub.2 OCH.sub.3 NHCOCH.sub.3 CH.sub.2 CHCHCl C.sub.6 H.sub.4 -2-CH.sub.3 blue14 Cl " OC.sub.2 H.sub.5 " CH.sub.2 CHCH.sub.2 " "15 Cl " " " CH.sub.3 C.sub.6 H.sub.4 -2-COOC.sub.2 H.sub.5 "16 Br " OCH.sub.3 NHCOCH.sub.3 CH.sub.2 CHCH.sub.2 C.sub.6 H.sub.4 -2-COOCH.sub.3 "17 Cl " " " H C.sub.6 H.sub.3 -2-CH.sub.3 -4-Cl "18 Cl " " " C.sub.2 H.sub.4 COOCH.sub.3 C.sub.6 H.sub.4 -4-COOCH.sub.3 "19 Cl " " " CH.sub.2 COOC.sub.2 H.sub.5 C.sub.6 H.sub.4 -4-CH.sub.3 "20 Cl " " " CH.sub.2 CHCH.sub.2 C.sub.6 H.sub.4 -2-CH(CH.sub.3).s ub.2 "21 Cl " " "n-C.sub.4 H.sub.9 C.sub.6 H.sub.4 -2-CH.sub.3 "22 Cl " " " CH.sub.2 CH(CH.sub.3)CH.sub.2 C.sub.6 H.sub.5 "23 Cl " " " CH.sub.2 CHCHCl C.sub.6 H.sub.4 -2-C.sub.2 H.sub.5 "24 Cl " " NHCOCH.sub.2 OCH.sub.3 " C.sub.6 H.sub.3 -2,6-(CH.sub.3).s ub.2 "25 Cl " " NHCOCH.sub.2 OH CH.sub.2 C.sub.6 H.sub.5 C.sub.6 H.sub.4 -2-CH(CH.sub.3).s ub.2 "26 Cl " " NHCOCH.sub.2 OCOCH.sub.3 CH.sub.2 CHCH.sub.2 (CH.sub.2).sub.3 Cl "27 Cl " " CH.sub.3 H C.sub.6 H.sub.3 -2,6-(CH.sub.3).s ub.2 violet28 Br " " " H " "29 Cl " " NHCOCH.sub.3 CH.sub.2 CHOHCH.sub.2 Cl C.sub.6 H.sub.4 -2-CH.sub.3 blue30 Cl " " " CH.sub.2 CH(OAc)OAc C.sub.6 H.sub.4 -2-OCH.sub.3 "31 Br " " " H C.sub.6 H.sub.4 -2-Allyl "32 Br " " " C.sub.2 H.sub.4 OCOCH.sub.3 C.sub.6 H.sub.4 -2-CH.sub.3 "33 I " " " " " "34 Cl " " " C.sub.2 H.sub.4 OCH.sub.3 C.sub.6 H.sub.4 -2-CH(CH.sub.3).s ub.2 "35 Cl " " " H C.sub.6 H.sub.4 -4-COOC.sub.4 H.sub.9 "36 Cl " " " (CH.sub.2).sub.4 OCOCH.sub.3 C.sub.6 H.sub.4 -2-CH.sub.3 "37 Cl " " " CH.sub.2 CH(OAc)CH.sub.3 " "38 Cl " " " (CH.sub.2).sub.3 2C.sub.6 H.sub.4 -2-C.sub.2 H.sub.5 "39 Cl " OC.sub.2 H.sub.5 NHCOCH.sub.3 H CH.sub.2 CH.sub.2 Cl "40 Cl " OCH.sub.3 NHCOOC.sub.2 H.sub.5 H (CH.sub.2).sub.3 Cl "41 Cl " " NHCOOCH.sub.3 H (CH.sub.2).sub.4 Br "42 Cl " " " H (CH.sub.2).sub.4 Cl "43 Cl " " " H (CH.sub.2).sub.3 C.sub.6 ".sub.544 Cl " " NHCOH H CH.sub.2 C.sub.6 H.sub.5 "45 Cl " " NHCOCHCH.sub.2 H " "46 Cl " " " H CH.sub.2 CH.sub.2 Cl "47 H Cl H NHCOCH.sub.3 CH.sub.2 CHCH.sub.2 C.sub.6 H.sub.3 -2,6-(CH.sub.3).s ub.2 rubin48 H CN H H " " "49 H " H H C.sub.2 H.sub.5 C.sub.6 H.sub.4 -2-COCH.sub.3 "50 H " H H CH.sub.3 C.sub.6 H.sub.4 -2-COC.sub.2 H.sub.5 "51 H " H H CH.sub.2 CHCHCl C.sub.6 H.sub.4 -2-CH.sub.3 "52 H Cl H NHCOCH.sub.3 CH.sub.2 CHCH.sub.2 C.sub.6 H.sub.4 -2-C.sub.2 H.sub.5 red53 H " H "n-C.sub.4 H.sub.9 C.sub.6 H.sub.4 -2-COOCH.sub.3 "54 H COOCH.sub.3 H H CH.sub.3 " scarlet55 H H H NHCOCH.sub.3 " C.sub.6 H.sub.4 -2-CH.sub.3 "56 Cl Cl H H " " yellow brown57 " " H H " C.sub.6 H.sub.4 -3-CH.sub.3 "__________________________________________________________________________
TABLE 2__________________________________________________________________________ ##STR27## NuanceExample R.sub.2 R.sub.1 R.sub.3 R.sub.5 on PES__________________________________________________________________________DK = 4-chloro-5-formyl-thiazolyl-2-58 OCH.sub.3 NHCOCH.sub.2 OC.sub.2 H.sub.5 H C.sub.6 H.sub.3 -2,4-(CH.sub.3).sub.2 blue59 " NHCOCH.sub.3 CH.sub.2 CHCH.sub.2 C.sub.6 H.sub.4 -2-CH.sub.3 "60 " CH.sub.3 H " violet61 H NHCOCH.sub.3 C.sub.2 H.sub.5 C.sub.6 H.sub.4 -2-CH(CH.sub.3).sub.2 "62 H H " C.sub.6 H.sub.4 -2-CH.sub.3 violet63 H H " C.sub.6 H.sub.3 -2-COOC.sub.2 H.sub.5 "64 H H CH.sub.3 C.sub.6 H.sub.4 -2-COC.sub.2 H.sub.5 rubin65 H OH CH.sub.2 CHCH.sub.2 C.sub.6 H.sub.4 -4-CH.sub.3 "DK = 4-Chlor-5-cyano-thiazolyl-2-66 H H C.sub.2 H.sub.5 C.sub.6 H.sub.3 -2,4-(CH.sub.3).sub.2 violet67 H NHCOCH.sub.3 " C.sub.6 H.sub.4 -2-CH.sub.3 blue68 OCH.sub.3 " H C.sub.6 H.sub.4 -2-COOCH.sub.3 "69 " " H " green70 H CH.sub.3 C.sub.2 H.sub.5 C.sub.6 H.sub.4 -2-C.sub.2 H.sub.5 blueDK = 5-Nitro-thiazolyl-2-71 OCH.sub.3 NHCOCH.sub.3 H C.sub.6 H.sub.3 -2,6-(CH.sub.3) blue72 H " C.sub.2 H.sub.5 C.sub.6 H.sub.4 -2-OCH.sub.3 "73 H CH.sub.3 " C.sub.6 H.sub.4 -2-CH.sub.3 violetDK = 4-Cyano-3-methyl-isothiazolyl-5-74 H H CH.sub.3 C.sub.6 H.sub.4 -2-CH.sub.3 red75 H H C.sub.2 H.sub.4 OCH.sub.3 C.sub.6 H.sub.3 -2,4-(CH.sub.3).sub.2 "76 H NHCOCH.sub.3 CH.sub.2 CCH.sub.2 C.sub.6 H.sub.3 -2,3-(CH.sub.3).sub.2 "DK = 3-Phenyl-1,2,4-thiadiazolyl-5-77 H H C.sub.2 H.sub.5 CH.sub.2 CH.sub.2 Br red78 H CH.sub.3 CH.sub.2 CHCHCH.sub.3 C.sub.6 H.sub.4 -2-CH.sub.3 "__________________________________________________________________________ NuanceEx. No. R.sub.50 R.sub.2 R.sub.1 R.sub.3 R.sub.5 on PES__________________________________________________________________________DK = 5-R.sub.50 mercapto-1,3,4-thiadiazolyl-2-79 5-C.sub.2 H.sub.5 H NHCOCH.sub.3 C.sub.2 H.sub.5 C.sub.2 H.sub.3 -2,4-(CH.sub.3).sub.2 red80 5-CH.sub.2 C.sub.6 H.sub.5 H " " CH.sub.2 C.sub.6 H.sub.5 "DK = Benzthiazolyl-2-substituted by R.sub.5081 (5),6,(7)Cl H CH.sub.3 CH.sub.3 C.sub.6 H.sub.4 -2-CH(CH.sub.3).sub.2 red82 6-NO.sub.2 H " C.sub.2 H.sub.5 C.sub.6 H.sub.4 -2-CH.sub.3 "DK = 5-Nitro-2,1-Benzisothiazolyl-3-83 H NHCOCH.sub.3 C.sub.2 H.sub.4 OCH.sub.3 CH.sub.2 CH.sub.2 Cl green blue84 H H C.sub.2 H.sub.5 C.sub.6 H.sub.4 -2-CH.sub.3 blueDK = 4-Chloro-3-cyano-5-formyl-thienyl-2-85 OCH.sub.3 NHCOCH.sub.3 H C.sub.6 H.sub.3 -2,4-(CH.sub.3).sub.2 green blue86 " NHCOCH.sub.2 OCH.sub.3 H " "87 " NHCOCH.sub.3 CH.sub.2 CHCH.sub.2 C.sub.6 H.sub.4 -2-CH.sub.3 "88 H " C.sub.2 H.sub.5 " blue89 H NHCOCH.sub.2 OCH.sub.3 " " "90 OCH.sub.3 CH.sub.3 H " "91 H " C.sub.2 H.sub.5 C.sub.6 H.sub.4 -2-CH(CH.sub.3).sub.2 red blueDK = 4-(substituierte)-3,5-dicyano-thienyl-2-92 4-Cl H CH.sub.3 C.sub.2 H.sub.5 C.sub.6 H.sub.4 -2-CH.sub.3 red blue93 " H NHCOCHCH.sub.2 " " blue94 " OC.sub.2 H.sub.5 NHCOC.sub.2 H.sub.4 Cl H C.sub.6 H.sub.4 -4-COOCH.sub.3 blue95 " H CH.sub.3 C.sub.2 H.sub.5 C.sub.6 H.sub.3 -2,4-(CH.sub.3).sub.2 red blue96 4-CH.sub.3 H " " C.sub.6 H.sub.3 -4-Cl-3-CH.sub.3 violet97 " H H " C.sub.6 H.sub.4 -2-Allyl rubinDK = 3-Cyano-5-nitro-thienyl-2-98 H CH.sub.3 C.sub.2 H.sub.5 CH.sub.2).sub.3 Cl blue99 H " " C.sub.6 H.sub.3 -2,6-(CH.sub.3).sub.2 "100 H NHCOCH.sub.3 " CH.sub.2 C.sub.6 H.sub.5 "DK = 3,5-Dinitro-thienyl-2-101 H NHCOCH.sub.3 C.sub.2 H.sub.5 C.sub.6 H.sub.4 -2-CH.sub.3 green102 H CH.sub.3 " C.sub.6 H.sub.4 -2-CH.sub.3 blue103 H H " C.sub.6 H.sub.4 -2-COOC.sub.2 ".sub.5DK = 3-Acetyl-5-nitro-thienyl-2-104 H CH.sub.3 C.sub.2 H.sub.5 C.sub.6 H.sub.3 -2,6-(CH.sub.3).sub.2 blue105 H "n-C.sub.4 H.sub.9 CH.sub.2 C.sub.6 H.sub.5 "DK = 3-Alkoxycarbonyl-5-nitro-thienyl-2-106 H CH.sub.3 C.sub.2 H.sub.5 CH.sub.2 CH.sub.2 CHClCH.sub.3 red blue107 H " " C.sub.6 H.sub.4 -2-CH.sub.3 "DK = 3-Cyano-5-(substituted)phenylazo-thienyl-2-108 (4'-H) H H C.sub.2 H.sub.5 C.sub.6 H.sub.4 -2-CH.sub.3 red blue109 " H H C.sub.2 H.sub.4 0COCH.sub.3 C.sub.6 H.sub.4 -2-CH(CH.sub.3).sub.2 "PYRAZOLE/IMIDAZOLE/TRIAZOLE:DK = 4-Cyano-3-methyl-1-phenyl-pyrazolyl-5-110 H NHCOCH.sub.3 C.sub.2 H.sub.5 C.sub.6 H.sub.4 -2-CH.sub.3 red111 H CH.sub.3 C.sub.2 H.sub.4 0CH.sub.3 C.sub.6 H.sub.4 -2-COOCH.sub.3 scarlet.DK = 1-Cyanomethyl-4,5-dicyano-imidazolyl-2-112 H CH.sub.3n-C.sub.6 H.sub.13 C.sub.6 H.sub.4 -2-CH.sub.3 red113 H " C.sub.2 H.sub.5 C.sub.6 H.sub.3 -2,4-(CH.sub.3).sub.2 "DK = 4-Cyano-1(substituted R.sub.50)1,2,3-triazolyl-5-114 (1-Allyl) H NHCOCH.sub.3 C.sub.2 H.sub.4 OCH.sub.3 C.sub.6 H.sub.4 -2-CH.sub.3 red115 (1-Benzyl) H NHCOCH.sub.2 OCH.sub.3 CH.sub.2 CHCH.sub.2 CH.sub.2 CH.sub.2 Cl "__________________________________________________________________________
The dyestuffs of the following formula ##STR28## in which the symbols are defined in Table 3 can be made from known compounds by an appropriate method of Examples 1 to 12.
TABLE 3__________________________________________________________________________ NuanceEx. No. R.sub.2 R.sub.1 R.sub.3 R.sub.5 on PES__________________________________________________________________________DK = 2,4-Dinitro-5-rhodano-phenyl-1-116 OC.sub.2 H.sub.5 NHCOCH.sub.2 OCH.sub.3 H CH.sub.2 CH.sub.2 Cl green blue117 OCH.sub.3 CH.sub.3 H C.sub.6 H.sub.4 -2-CH.sub.3 blue118 H NHCOCH.sub.3 C.sub.2 H.sub.5 C.sub.6 H.sub.4 -2-OCH.sub.3 "119 H CH.sub.3 " " "120 H H " C.sub.6 H.sub.4 -4-COOC.sub.2 H.sub.5 red blueDK = 2,4-Dinitro-5-chloro-phenyl-1-121 OCH.sub.3 NHCOCH.sub.3 H C.sub.6 H.sub.4 -2-CH(CH.sub.3).sub.2 blue122 " NHCOC.sub.2 H.sub.5 H C.sub.6 H.sub.4 -2-CH.sub.3 "123 " NHCOOCH.sub.3 CH.sub.2 CHCH.sub.2 C.sub.6 H.sub.4 -4-CH.sub.3 "DK = 2,4-Dinitro-5,6-dichloro-phenyl-1-124 " NHCOCH.sub.3 (CH.sub.2).sub.3 CN CH.sub.2 CH.sub.2 Cl blue125 " " H C.sub.6 H.sub.4 -4-COOCH.sub.3 "DK = 2,6-Dicyano-4-methyl-phenyl-1-126 H NHSO.sub.2 CH.sub.3 C.sub.2 H.sub.5 (CH.sub.2).sub.3 Cl red127 H " " C.sub.6 H.sub.4 -2-CH.sub.3 "128 H CH.sub.3 " " "DK = 2,6-Dicyano-4-bromo-phenyl-1-129 H OH CH.sub.2 CHCH.sub.2 C.sub.6 H.sub.3 -2-CH.sub.3 red130 H " C.sub.2 H.sub.5 C.sub.6 H.sub.3 -2,4-(CH.sub.3).sub.2 "__________________________________________________________________________
Compounds of the formula ##STR29## in which the symbols are defined in Table 4 can be prepared from known compounds by an appropriate method of Example 1 to 12.
TABLE 4______________________________________Ex. NuanceNo. R.sub.6 R.sub.7 R.sub.3 R.sub.4 on PES______________________________________131 --CN H --C.sub.2 H.sub.5 H Rubine132 Cl Cl --CH.sub.3 H yellow brown133 --CN H --CH.sub.2 CH.sub.2 O--CO--OCH.sub.3 H Red134 " H --CH.sub.2 CH.sub.2 O--COCH.sub.3 H "135 Cl Cl --CH.sub.3 --CH.sub.3 yellow brown______________________________________
Compounds of the formula ##STR30## in which the symbols are defined in Table 5 can be prepared from known compounds by an appropriate method of Example 1 to 12.
TABLE 5__________________________________________________________________________ NuanceEx. No. R.sub.7 R.sub.6 R.sub.2 R.sub.1 R.sub.3 R.sub.5 on PES__________________________________________________________________________136 Cl --NO.sub.2 --OCH.sub.3 --NHCOCH.sub.3 H --CH.sub.3 blue137 Cl " " " H --C.sub.2 H.sub.5 "138 Cl " " " H --C.sub.4 H.sub.9 -n "139 H --CN H H --CH.sub.3 --C.sub.2 H.sub.5 rubin140 Cl Cl H H " " yellow brown__________________________________________________________________________
Compounds of the formula ##STR31## in which the symbols are defined in Table 6 can be prepared from known compounds by an appropriate method of Example 1 to 12.
TABLE 6__________________________________________________________________________Ex. No R.sub.6 R.sub.7 R.sub.1 R.sub.2 R.sub.3 R.sub.x Nuance on PES__________________________________________________________________________141 --NO.sub.2 Br --NHCOCH.sub.3 H --C.sub.2 H.sub.5 H violet142 " Cl " H --C.sub.4 H.sub.9 H "143 " " " H --(CH.sub.2).sub.4 OCOCH.sub.3 H "144 " " --CH.sub.3 OCH.sub.3 --CH.sub.3 H "145 " " " " --C.sub.2 H.sub.4 OCOCH.sub.3 H "146 " " " " H H "147 " " " " H 4-NO.sub.2 "148 " Br " " H H "149 " H --NHCOCH.sub.3 H --CH.sub.2 CH.dbd.CH--Cl H ruby red150 " H " H --CH.sub.2 CH.dbd.CH.sub.2 H "151 " H H H -- CH.sub.3 H "152 --CN H H H --C.sub.2 H.sub.5 H "153 " H H H --CH.sub.2 CH.dbd.CH.sub.2 H "154 --CN H H H --CH.sub.3 H ruby red155 " H --NHCOCH.sub.3 H --CH.sub.2 CH.dbd.CH.sub.2 H "156 " H --NHCOC.sub.2 H.sub.5 H --C.sub.2 H.sub.4 OCH.sub.3 H "157 Cl H --NHCOCH.sub.3 H --C.sub.2 H.sub.5 H red158 H H H H --C.sub.2 H.sub.4 OCOC.sub.2 H.sub.5 H scarlet159 Cl Cl H H --CH.sub.3 H yellow brown160 " " H H --C.sub.2 H.sub.5 H "161 --NO.sub.2 Cl --NHCOCH.sub.3 --OCH.sub.3 --CH.sub.2 C.tbd.CH H navy blue162 " " " " " 4-NO.sub.2 "163 " Br " " H " "164 " " --NHCOOCH.sub.3 --OC.sub.2 H.sub.5 H H "165 " " " --OCH.sub.3 H 4-NO.sub.2 "166 " " " " --CH.sub.2 C.tbd.CH " "167 " Cl --NHCOCH.sub.3 " --CH.sub.2 COOCH.sub.3 H "168 " " " " --CH.sub.2 COOCH.sub.2 C.tbd.CH H "169 " " --NHCOC.sub.2 H.sub.5 " H H "170 " " --NHCOOCH.sub.3 " H H "171 " " --NHCOOCH.sub.3 " H 4-Cl "172 " " --NHCOCH.dbd.CH.sub.2 " H H "173 " " --NHCOCH.sub.3 " --CH.sub.2 CH.dbd.CH--Cl H "174 " " " --OC.sub.2 H.sub.5 --C.sub.2 H.sub.4 COOCH.sub.3 H "175 " " " " --(CH.sub.2).sub.3 CN H "176 " " " --OCH.sub.3 --C.sub.2 H.sub.4 OCOCH.sub.3 H "177 " " " " --C.sub.2 H.sub.4 COOCH.sub.2 C.tbd.CH H "178 " " " " --CH.sub.2 COOC.sub.6 H.sub.5 H "179 " " " " --C.sub.2 H.sub.4 OCH.sub.3 4-CH.sub.3 "180 " " " --OC.sub.2 H.sub.5 --CH.sub.2 C.dbd.CH 4-NO.sub.2 "__________________________________________________________________________
Compounds of the formula ##STR32## in which the symbols are defined in Table 7 can be prepared from known compounds by an appropriate method of Example 1 to 12.
TABLE 7__________________________________________________________________________ NuanceEx. No. R.sub.8 R.sub.6 R.sub.7 R.sub.1 R.sub.2 R.sub.3 Z on PES__________________________________________________________________________181 H NO.sub.2 Cl NHCOCH.sub.3 OCH.sub.3 H ##STR33## navy blue182 H " Br " " H " "183 H " Cl " " CH.sub.2 CCH " "184 H " " " OC.sub.2 H.sub.5 CH.sub.2 COOCH.sub.3 " "185 H " " NHCOC.sub.2 H.sub.5 OCH.sub.3 H " "186 H " " CH.sub.3 " H " violet187 H CN H H H C.sub.2 H.sub.5 " ruby red188 H " H H H CH.sub.2 CHCH.sub.2 " "189 H Cl Cl H H CH.sub.3 " yellow brown190 H " " H H C.sub.2 H.sub.5 " yellow brown191 H NO.sub.2 " NHCOCH.sub.3 OCH.sub.3 H C.sub.2 H.sub.4 C.sub.6 H.sub.5 navy blue192 H " Br " " H " "193 H " Cl " " CH.sub.2 CCH " "194 H " " " " CH.sub.2 CHOHCH.sub.2 Cl " "195 H " " NHCOCH.sub.3 " H (CH.sub.2).sub.3 C.sub.6 H.sub.5 "196 H " " NHCHO " H " "197 H " Br NHCOCH.sub.3 " H " "198 Cl " Cl " " H CH.sub.2 C.sub.6 H.sub.5 "199 Cl " " " " CH.sub.2 CCH " "200 Cl " " H " CH.sub.2 CHCH.sub.2 " "__________________________________________________________________________
Compounds of the formula ##STR34## in which the symbols are defined in Table 8 can be prepared from known compounds by an appropriate method of Example 1 to 10.
__________________________________________________________________________ NuanceEx. No. R.sub.30 Z R.sub.1 R.sub.2 R.sub.3 on PES__________________________________________________________________________201 O CCN CH.sub.3 H C.sub.2 H.sub.5 blue202 O " " H C.sub.4 H.sub.9 "203 CHNO.sub.2 " " H C.sub.2 H.sub.5 green blue204 C(CN)COOC.sub.2 H.sub.5 " " H " " C(CN)COOC.sub.4 H.sub.9 (n) (1:1 ratio)205 O " NHCOCH.sub.3 H " blue206 O N CH.sub.3 H " violet207 O " NHCOCH.sub.3 OCH.sub.3 H navy blue208 O " " " CH.sub.2 CHCH.sub.2 "209 O " " " CH.sub.2 CHCHCl "210 O " " OC.sub.2 H.sub.5 H "211 O " " " CH.sub.2 CHCH.sub.2 "212 O " " " CH.sub.2 CCH "213 O.sub.2 NCH " CH.sub.3 H C.sub.2 H.sub.5 blue214 ##STR35## " " H " "215 ##STR36## " " OCH.sub.3 H green blue__________________________________________________________________________
Compounds of the formula ##STR37##
in which the symbols are defined in Table 9 can be prepared from known compounds by an appropriate method of Example 1 to 12.
TABLE 9__________________________________________________________________________Ex. No. DK R.sub.1 R.sub.2 Y R.sub.3 Nuance on__________________________________________________________________________ PES216 ##STR38## H H C.sub.3 H.sub.6 CH.sub.3 rubin217 " H H ##STR39## " "218 ##STR40## NHCOCH.sub.3 OCH.sub.3 " H navy blue219 ##STR41## " OC.sub.2 H.sub.5 " " "220 ##STR42## CH.sub.3 H " C.sub.2 H.sub.5 scarlet red__________________________________________________________________________
TABLE 10__________________________________________________________________________Example No. Nuance on__________________________________________________________________________ PES221 ##STR43## navy blue222 ##STR44## navy blue223 ##STR45## navy blue224 ##STR46## navy blue225 ##STR47## yellow brown226 ##STR48## yellow brown227 ##STR49## yellow228 ##STR50## navy blue229 ##STR51## blue230 ##STR52## blue231 ##STR53## blue232 ##STR54## navy blue233 ##STR55## blue234 ##STR56## blue235 ##STR57## blue236 ##STR58## navy blue237 ##STR59## greenish blue238 ##STR60## blue239 ##STR61## blue240 ##STR62## navy blue241 ##STR63## greenish blue242 ##STR64## blue__________________________________________________________________________
Compounds of the formula ##STR65## in which the symbols are defined in Table 11 can be prepared from known compounds by an appropriate method of Example 1 to 12.
TABLE 11__________________________________________________________________________Ex. No. R.sub.6 R.sub.7 R.sub.1 R.sub.2 R.sub.3 Z Nuance on__________________________________________________________________________ PES243 CN H H H CH.sub.3 CH.sub.2 CHCH ruby red244 " H H H " CH.sub.2 CHCHCl "245 " H H H " CH.sub.2 CCH "246 " H H H " CH.sub.2 CH.sub.2 Br "247 " H H H " CH.sub.2 CH.sub.2 Cl "248 " H H H " ##STR66## "249 " H H H " ##STR67## "250 " H H H n-C.sub.4 H.sub.9 C.sub.6 H.sub.5 "251 CN H H H CH.sub.3 ##STR68## ruby red252 " H H H C.sub.2 H.sub.5 " "253 " H H H CH.sub.3 ##STR69## "254 " H H H " ##STR70## "255 " H H H " ##STR71## "256 " H H H " ##STR72## "257 " H H H CH.sub.3 ##STR73## ruby red258 " H H H " ##STR74## "259 " H H H " ##STR75## "260 " H H H " ##STR76## "261 NO.sub.2 Cl NHCOCH.sub.3 OCH.sub.3 H CH.sub.2 CHCH.sub.2 navy blue262 " Cl " " CH.sub.2 CHCH.sub.2 " "263 " Br " OC.sub.2 H.sub.5 " CH.sub.2 CHCHCl "264 " Cl " " H " "265 " Cl " OCH.sub.3 H CH.sub.2 CHCH "266 " Br " " CH.sub.2 CHCHCl " "267 " Cl NHCOC.sub.2 H.sub.5 " H CH.sub.2 CH.sub.2 Cl "268 " Cl NHCOCH.sub.3 " CH.sub.2 CHCH.sub.2 " "269 " Cl NHCOCH.sub.3 OC.sub.2 H.sub.5 CH.sub.2 CHCH.sub.2 " navy blue270 " Cl " OCH.sub.3 H " "271 NO.sub.2 Cl NHCOCH.sub.3 OC.sub.2 H.sub.5 H ##STR77## "272 " " " " CH.sub.2 CCH " "273 " " " " H " "274 " Br " OCH.sub.3 H C.sub.6 H.sub.5 "275 " Br NHCOCHCH.sub.2 " CH.sub.2 CHCH.sub.2 " "276 " Cl " " H ##STR78## "277 NO.sub.2 Cl NHCOCH.sub.3 " CH.sub.2 CHCH.sub.2 ##STR79## "278 " Cl " OC.sub.2 H.sub.5 H ##STR80## "279 " Cl " OCH.sub.3 CH.sub.2 CHCHCl CH.sub.2 CH.sub.2 Cl "280 " Cl " " CH.sub.2 CHCH.sub.2 ##STR81## "281 Cl Cl H H CH.sub.3 CH.sub.2 CHCH.sub.2 yellow brown282 Cl Cl H H " CH.sub.2 CHCHCl "283 Cl Cl H H " CH.sub.2 CHCH "284 Cl Cl H H " ##STR82## "285 Cl Cl H H " ##STR83## "286 Cl Br H H CH.sub.2 CH.sub.3 " "287 Cl Cl H H CH.sub.3 C.sub.6 H.sub.5 yellow brown288 Cl Cl H H CH.sub.2 CH.sub.3 ##STR84## "289 Cl Cl H H CH.sub.2 CHCH.sub. 2 ##STR85## "290 Cl Cl H H CH.sub.3 ##STR86## "291 Cl Cl H H " ##STR87## "292 Cl Cl H H " ##STR88## "293 Cl Cl H H " ##STR89## "294 NO.sub.2 Br NHCOCH.sub.3 H CH.sub.2 CH.sub.3 " violet295 " Cl " H " CH.sub.2 CHCH.sub.2 "296 CN CN CH.sub.3 H C.sub.3 H.sub.7 CH.sub.2 CHCH.sub.2 blue297 NO.sub.2 " " H C.sub.4 H.sub.9 ##STR90## "298 " H NHCOCHCH.sub.2 H CH.sub.3 CH.sub.2 CHCH.sub.2 ruby__________________________________________________________________________ red
Compounds of the formula ##STR91## in which the symbols are defined in Table 12 can be prepared from known compounds by an appropriate method of Example 1 to 12.
TABLE 12__________________________________________________________________________Ex No R.sub.6 R.sub.7 R.sub.1 R.sub.2 R.sub.3 R.sub.x Nuance on PES__________________________________________________________________________299 --CN H H H CH.sub.3 H ruby red300 " H H H --CH.sub.2 CH.sub.3 H "301 " H H H --CH.sub.2 CH.dbd.CH.sub.2 H "302 " H H H --CH.sub.3 4-NO.sub.2 "303 --NO.sub.2 H --NHCOCH.sub.3 H --CH.sub.2 CH.dbd.CH.sub.2 H "304 " H --NHCOC.sub.2 H.sub.5 H --CH.sub.2 C.tbd.CH H "305 " H --NHCOCH.dbd.CH.sub.2 H --CH.sub.2 CH.dbd.CH.sub.2 H "306 " Cl --NHCOCH.sub.3 --OCH.sub.3 H H navy blue307 " Br " " H H "308 " Cl " OCH.sub.2 CH.sub.3 H H "309 " Cl " --OCH.sub.3 --CH.sub.2 CH.dbd.CH.sub.2 H "310 " Cl " " --CH.sub.2 CH.dbd.CHCl H "311 " Cl --NHCOCH.sub.2 CH.sub.3 " H H "312 " Cl --NHCO--OCH.sub.3 " --CH.sub.2 CH.dbd.CH.sub.2 H "313 " Cl --NHCOCH.sub.3 " H 4-NO.sub.2 "314 " Br " " --CH.sub.2 CH.dbd.CH.sub.2 H "315 " Br " " --CHC.tbd.CH H "316 " Cl " " " H "317 Cl Cl H H --CH.sub.3 H yellow brown318 Cl Cl H H " 4-NO.sub.2 "__________________________________________________________________________
Compounds of the formula ##STR92## in which the symbols are defined in Table 13 can be prepared from known compounds by an appropriate method of Example 1 to 12.
TABLE 13__________________________________________________________________________ NuanceEx. No. R.sub.6 R.sub.7 R.sub.3 R.sub.4 R.sub.5 Polyester__________________________________________________________________________319 Cl Cl --CH.sub.3 H --CH.sub.3 yellow brown320 Cl Cl --CH.sub.3 --CH.sub.3 H "321 Br Br --CH.sub.3 H H "322 --CN H --CH.sub.2 C.sub.6 H.sub.5 H H ruby red323 " H --CH.sub.2 CH.sub.2 --C.sub.6 H.sub.5 H H "324 " H --CH.sub.2 CH.sub.2 OC.sub.6 H.sub.5 H H "325 " H --CH.sub.2 CH.sub.2 O--CO--OCH.sub.3 H H bluish red326 " H --CH.sub.2 CH.dbd.CH.sub.2 H H ruby red327 Cl Cl --CH.sub.2 CH.sub.3 H H yellow brown328 --CN H --CH.sub.2 C.tbd.CH H H ruby red329 " H --CH.sub.3 H --CH.sub.3 "330 " H --CH.sub.2 CH.sub.2 OCOOC.sub.2 H.sub.5 H H "331 Br Cl --CH.sub.3 H H yellow brown__________________________________________________________________________
Compounds of the formula ##STR93## in which the symbols are defined in Table 14 can be prepared from known compounds by an appropriate method of Example 1 to 12.
TABLE 14__________________________________________________________________________Ex. No. DK R.sub.1 R.sub.2 R.sub.3 Nuance on__________________________________________________________________________ PES332 ##STR94## H H C.sub.2 H.sub.5 ruby333 ##STR95## H H C.sub.4 H.sub.9 "334 " H H CH.sub.2 CH.sub.2 CN red335 ##STR96## H H CH.sub.3 "336 ##STR97## H H C.sub.2 H.sub.4 CN scarlet337 ##STR98## H H " "338 ##STR99## NHCOCH.sub.3 H " red339 " " Cl H scarlet340 ##STR100## " " H ruby341 ##STR101## H H CH.sub.3 "342 ##STR102## H H CH.sub.2 CHCH.sub.2 yellow brown343 ##STR103## H H C.sub.4 H.sub.9 "344 ##STR104## H H CH.sub.2 CHCH.sub.2 "345 ##STR105## H H " "346 ##STR106## NHCOCH.sub.3 C.sub.2 H.sub.5 bluish violet347 ##STR107## CH.sub.3 H C.sub.4 H.sub.9 reddish blue348 " NHCOCH.sub.3 H C.sub.3 H.sub.7 blue349 " NHCOC.sub.2 H.sub.5 H " "350 " NHCOCH.sub.3 H C.sub.2 H.sub.5 /C.sub.3 H.sub.7 (1:1) "351 ##STR108## CH.sub.3 H C.sub.2 H.sub.5 scarlet352 " NHCOC.sub.2 H.sub.5 H C.sub.2 H.sub.5 bluish red353 " NHSO.sub.2 CH.sub.3 H C.sub.2 H.sub.5 /C.sub.3 H.sub.7 (1:1) red354 ##STR109## NHCOC.sub.2 H.sub.5 H " ruby355 ##STR110## CH.sub.3 H C.sub.4 H.sub.9 bluish violet356 ##STR111## H H CH.sub.3 bluish red357 " CH.sub.3 H C.sub.2 H.sub.5 violet358 " NHCOCH.sub.3 H C.sub.2 H.sub.4 CN bluish red359 ##STR112## CH.sub.3 H C.sub.2 H.sub.5 scarlet360 " NHCOC.sub.2 H.sub.5 H " red361 ##STR113## H H C.sub.2 H.sub.5 scarlet362 " CH.sub.3 H " red363 " NHCOCH.sub.3 H " ruby364 " " H C.sub.2 H.sub.4 CN red365 ##STR114## CH.sub.3 H C.sub.4 H.sub.9 bluish red366 ##STR115## " H C.sub.2 H.sub.5 dark blue367 " NHCOCH.sub.3 H C.sub.2 H.sub.5 /C.sub.3 H.sub.7 (1:1) greenish blue368 ##STR116## H H C.sub.2 H.sub.5 blue369 " CH.sub.3 H " greenish blue370 " H H C.sub.2 H.sub.4 OCOCH.sub.3 reddish blue371 " NHCOCH.sub.3 H C.sub.2 H.sub.5 bluish green372 ##STR117## CH.sub.3 H C.sub.4 H.sub.9 reddish blue373 ##STR118## " H C.sub.2 H.sub.5 reddish navy374 ##STR119## H H " dark blue375 ##STR120## H H " "376 ##STR121## H H C.sub.2 H.sub.5 greenish blue377 ##STR122## NHCOCH.sub.3 H CH.sub.2 CCH red378 " " H " bluish red379 ##STR123## H H C.sub.2 H.sub.5 violet380 ##STR124## H H C.sub.2 H.sub.4 CN violet381 ##STR125## CH.sub.3 H C.sub.2 H.sub.5 "382 " " H CH.sub.3 "383 ##STR126## CH.sub.3 H " ruby384 " H H C.sub.2 H.sub.5 red385 ##STR127## NHCOC.sub.2 H.sub.5 H " blue386 ##STR128## NHCOCH.sub.3 H " "387 " " H C.sub.2 H.sub.5 /C.sub.3 H.sub.7 (1:1) "388 ##STR129## " H " bluish violet389 ##STR130## NHCOCH.sub.3 H C.sub.2 H.sub.5 "390 ##STR131## " H " red__________________________________________________________________________
Compounds of the formula ##STR132## in which the symbols are defined in Table 15 can be prepared from known compounds by an appropriate method of Example 1 to 12.
TABLE 15__________________________________________________________________________Ex. No. M R.sub.7 R.sub.8 R.sub.3 Nuance on PES__________________________________________________________________________391 H --Br --CH.sub.3 H navy blue392 H " --C.sub.2 H.sub.5 H "393 H " --C.sub.2 H.sub.4 OCH.sub.3 H "394 H Cl --CH.sub.3 H "395 Cl " " H "396 H " --C.sub.2 H.sub.4 OCH.sub.3 H "397 H " --C.sub.2 H.sub.5 H "398 H " --CH.sub.3 --C.sub.2 H.sub.5 greenish navy blue399 H " " --CH.sub.2 --CH.dbd.CH.sub.2 navy blue400 H Br " --CH.sub.2 --CH.dbd.CHCl reddish navy blue401 H Cl " --CH.sub.2 --CH.dbd.CH.sub.2 "402 H " " --CH.sub.2 --C.sub.6 H.sub.5 navy blue403 H " --C.sub.2 H.sub.5 --CH.sub.2 --CH.dbd.CH.sub.2 "404 H " " --CH.sub.2 --CH.dbd.CH--Cl "405 H " " --CH.sub.3 --C.tbd.CH reddish navy blue406 H Cl --CH.sub.3 --C.sub.2 H.sub.4 --C.sub.6 H.sub.5 greenish navy blue407 H " " --C.sub.3 H.sub.6 O--C.sub.6 H.sub.5 "408 H H " --CH--CH.dbd.CH--Cl reddish navy blue409 H --I " --CH.sub.2 CH.dbd.CH.sub.2 "410 H --CN " " greenish blue411 H " " --C.sub.2 H.sub.5 bluish green__________________________________________________________________________
Compounds of the formula ##STR133## in which the symbols are defined in Table 16 can be prepared from known compounds by an appropriate method of Example 1 to 12.
TABLE 16__________________________________________________________________________ Nuance onEx. No. R.sub.40 Z R.sub.1 R.sub.2 R.sub.3 PES__________________________________________________________________________412 O CCN CH.sub.3 H C.sub.2 H.sub.5 blue413 O " " H C.sub.4 H.sub.9 "414 ##STR134## " " H C.sub.2 H.sub.5 greenish- blue415 ##STR135## " " H " "416 O " NHCOCH.sub.3 H " red blue417 O N CH.sub.3 H " violet418 O " NHCOCH.sub.3 OCH.sub.3 H navy blue419 O " " " CH.sub.2 CHCH.sub.2 "420 O " " " CH.sub.2 CHCHCl "421 O " " OC.sub.2 H.sub.5 " "422 O " " " CH.sub.2 CHCH.sub.2 "423 O " " OC.sub.2 H.sub.4 COCH.sub.3 " "424 O " " OC.sub.2 H.sub.5 " "425 O.sub.2 NCH " CH.sub.3 H C.sub.2 H.sub.5 blue426 ##STR136## " " H " "__________________________________________________________________________
Compounds of the formula ##STR137## in which the symbols are defined in Table 17 can be prepared from known compounds by an appropriate method of Example 1 to 12.
__________________________________________________________________________ Nuance onEx. No. DK R.sub.1 R.sub.2 Y R.sub.3 PES__________________________________________________________________________427 ##STR138## H H CH.sub.2 CH.sub.2 CH.sub.2 CH.sub.3 ruby428 " H H ##STR139## " "429 ##STR140## NHCOCH.sub.3 OCH.sub.3 " H marine blue430 ##STR141## " OC.sub.2 H.sub.5 " H "431 ##STR142## CH.sub.3 H " C.sub.2 H.sub.5 scarlet red__________________________________________________________________________
EXAMPLE 432-433
The following compounds can be prepared analogously to an appropriate method of Examples 1 to 12. ##STR143##
EXAMPLE 434
16.3 parts of 2-amino-5-nitrobenzonitrile are stirred into 100 parts of 93% cold sulphuric acid and are then reacted, over 30 minutes with 32 parts of 40% nitrosylsulphuric acid at 0.degree.-5.degree. C.
The resultant diazonium solution is stirred for 3 to 4 hours at 0.degree.-5.degree. C. and is then poured onto a mixture of 26.1 parts of 3-(N-methyl-N-phenylamino)propionic acid-2'-trifluoroethyl ester, 100 parts of glacial acetic acid, 2 parts of amidosulphonic acid, 200 parts of water and 500 parts of ice.
The resultant precipitated dyestuff is filtered, washed salt free with water and dried under vacuum at 60.degree. C. The purification,the dyestuff can be recrystallized or column chromatographed. The resulting dyestuff is of the formula 434a ##STR144##
This dyestuff can dye polyester material a ruby red colour and has excellent fastness properties, especially good wet fastness properties after thermofixation at 180.degree. C. This dyestuff is particularly suited for modern Rapid Dyeing processes.
.lambda.max=538 nm (DMF).
EXAMPLE 435
21.8 parts of 2-chloro-4,6-di-nitroaniline are stirred into 150 parts of 93% sulphuric acid at 15.degree.-20.degree. C. and are then reacted, over 30 minutes with 32 parts of 40% nitrosylsulphuric acid.
This is stirred for 2 to 3 hours and the resultant diazonium solution is poured over 15-20 minutes, onto a mixture of 41 parts of 3-(N-3'"-chloroallyl-N-5"-acetylamino-2"-methoxyphenylamino)propionic acid-2'-trifluoroethyl ester, 100 parts of glacial acetic acid, 2 parts of amidosulphonic acid and 300 parts of ice. To complete the coupling, sodium acetate is added.
The resultant precipitated dyestuff is filtered, washed salt free with water and dried under vacuum at 60.degree. C. The resulting dyestuff is then recrystallised or column chromatographed to purify the product. The product is a compound of the formula 435a ##STR145##
This dyestuff can dye polyester material a navy blue colour and has excellent fastness properties, especially good wet fastness properties. This dyestuff is particularly suited for modern Rapid Dyeing processes. The .lambda.max=595 nm (DMF).
EXAMPLE 436
18.7 parts of 2-amino-4-chloro-3-cyano-5-formyl-thiophene are dissolved in 200 parts of 85% phosphoric acid at -10.degree. to -5.degree. C. Whilst stirring, 33.3 parts of 40% nitrosyl sulphuric acid are added and the mixture stirred for about 3-4 hours at about 0.degree. C. The resulting solution is added whilst stirring well, to a solution of 27.5 parts of 3-(N-ethyl-N-3"-methylphenylamino)-propionic acid-2'-trifluoroethyl ester, 250 parts of glacial acetic acid, 80 parts water and 1000 parts of ice. The mixture is stirred for 30 minutes and then diluted slowly with 2000 parts of icewater. The dyestuff suspension is filtered and washed acid free with water. The product is dried under vacuum at 50.degree. C.
The resulting dyestuff is then recrystallised or column chromatographed to purify the product. A dyestuff of the formula 436a ##STR146## results.
This dyestuff dyes polyester fibres a clear reddish blue tone with good fastness properties, especially good wet fastness properties (ie in the C4A wash test from M&S) after thermofixing at 180.degree. C. The product is particularly suitable for Rapid Dyeing processes.
EXAMPLES 437-503
In Table 18, compounds of the formula ##STR147## where the symbols are as defined in Table 18 as well as the dyes of Tables 19-21 can be made analogously to Examples 434-436 from appropriate reactants.
TABLE 18__________________________________________________________________________Ex. No. DK R.sub.1 R.sub.2 R.sub.3 Nuance on__________________________________________________________________________ PES437 ##STR148## H H CH.sub.2 C.sub.6 H.sub.5 ruby red438 " H H C.sub.2 H.sub.5 "439 " H H C.sub.2 H.sub.4 CN "440 " H H C.sub.2 H.sub.4 OCOCH.sub.3 "441 ##STR149## H H CH.sub.3 "442 ##STR150## NHCOCH.sub.3 H C.sub.2 H.sub.2 CN red443 " " Cl H scarlet444 ##STR151## " " H ruby red445 ##STR152## H H C.sub.2 H.sub.5 yellow brown446 ##STR153## H H CH.sub.2 C.sub.6 H.sub.5 "447 ##STR154## H H CH.sub.2 CH.sub.2 CN yellow brown448 ##STR155## CH.sub.3 H C.sub.4 H.sub.9 -n reddish blue449 " NHCOCH.sub.3 H C.sub.3 H.sub.7 -n blue450 " NHCOC.sub.2 H.sub.5 H C.sub.3 H.sub.7 -n "451 ##STR156## CH.sub.3 H C.sub.2 H.sub.5 scarlet452 " NHCO.sub.2 C.sub.2 H.sub.5 H " blue red453 ##STR157## CH.sub.3 H C.sub.4 H.sub.9 n bluish violet454 ##STR158## H H CH.sub.3 bluish red455 " CH.sub.3 H C.sub.2 H.sub.5 Violet456 " NHCOCH.sub.3 H C.sub.2 H.sub.4 CN bluish red457 ##STR159## H H C.sub.2 H.sub.5 scarlet458 " CH.sub.3 H " red459 ##STR160## " H C.sub.2 H.sub.4 CN red460 ##STR161## CH.sub.3 H C.sub.4 H.sub.9 n bluish red461 ##STR162## " H C.sub.2 H.sub.5 dark blue462 " NHCOCH.sub.3 H C.sub.2 H.sub.5 /C.sub.3 H.sub.7 (1:1) greenish blue463 ##STR163## H H C.sub.2 H.sub.5 blue464 " CH.sub.3 H " greenish blue465 " NHCOCH.sub.3 H C.sub.2 H.sub.5 green466 ##STR164## CH.sub.3 H C.sub.4 H.sub.9 n reddish blue467 ##STR165## H H " dark blue468 ##STR166## H H C.sub.2 H.sub.5 greenish navy469 ##STR167## NHCOC.sub.2 H.sub.5 H " blue470 " NHCOCH.sub.3 H " blue471 " " H C.sub.2 H.sub.5 /C.sub.3 H.sub.7 -n (1:1) "472 ##STR168## " H " bluish violet473 " NHCOC.sub.2 H.sub.5 H " "474 ##STR169## " H " red__________________________________________________________________________
TABLE 19__________________________________________________________________________ ##STR170##Ex. No. M R.sub.7 R.sub.8 R.sub.3 Nuance on PES__________________________________________________________________________475 H Br CH.sub.3 H navy blue476 H " C.sub.2 H.sub.5 H "477 H Cl CH.sub.3 H "478 Cl Cl CH.sub.3 H "479 H " C.sub.2 H.sub.4 OCH.sub.3 H "480 H " " CH.sub.2 CHCH.sub.2 greenish navy481 H Br " CH.sub.2 CHCHCl reddish navy482 H " " CH.sub.2 CCH "483 H " C.sub.2 H.sub.5 H navy blue484 H " " CH.sub.2 CHCH.sub.2 greenish navy485 H " CH.sub.3 CH.sub.2 CHCHCl reddish navy486 H CN " " greenish blue487 H Cl " CH.sub.2 COOCH.sub.2 CCH reddish navy blue488 H " " CH.sub.2 COOCH.sub.2 CHCH.sub.2 "489 H " " CH.sub.2 COOC.sub.2 H.sub.5 "__________________________________________________________________________
TABLE 20__________________________________________________________________________ ##STR171##Ex. No. R.sub.40 Z R.sub.1 R.sub.2 R.sub.3 Nuance on__________________________________________________________________________ PES490 O CCN CH.sub.3 H C.sub.2 H.sub.5 bluish violet491 O " " H C.sub.4 H.sub.9 -n "492 CHNO.sub.2 " " H C.sub.2 H.sub.5 blue493 C(CN)COOC.sub.2 H.sub.5 " " H " " C(CN)COOC.sub.4 H.sub.9 n (1:1 ratio)494 O N NHCOCH.sub.3 OCH.sub.3 H navy blue495 O N " " CH.sub.2 CHCH.sub.2 reddish navy496 O " " OCH.sub.3 CH.sub.2 CHCHCl "497 O " " OC.sub.2 H.sub.5 " "498 O " " " CH.sub.2 CHCH.sub.2 "499 O " " OC.sub.2 H.sub.5 " "__________________________________________________________________________
TABLE 20__________________________________________________________________________Ex. No. Nuance on PES__________________________________________________________________________500 blue ##STR172##501 navy blue ##STR173##502 blue ##STR174##503 ruby red ##STR175##__________________________________________________________________________
EXAMPLE 504
17.4 parts of 1-amino-2,4-dinitro-6-chlorobenzene are dissolved in 137 parts of 93% sulphuric acid. The mixture is cooled to 10.degree. to 15.degree. C. Whilst stirring well, 33.3 parts of 40% nitrosyl sulphuric acid are added and the mixture stirred for about 1 hour at about 0.degree. C. The resulting solution is added over 15 minutes to a solution of 40 parts of 3-(N-allyl-N-2"-methoxy-5"-acetylamino-phenylamino)propionic acid-2'-tetrafluoropropyl ester, 500 parts of water and 800 parts of icewater. To complete the reaction sodium acetate is added. The dyestuff suspension is filtered and washed acid free with water. The product is dried under vacuum at 50.degree. C. The resulting dyestuff is then recrystallised or column chromatographed to purify the product. A dyestuff of the formula 504a ##STR176## results.
This dyestuff dyes polyester fibres a navy blue tone with good fastness properties.
In the Examples where column chromatography is performed the eluent is ethylmethylketone/toluene.
Application Example
The dyestuff of Example 1 (of formula 1a) is sandmilled with a commercially available dispersing agent, for example a commercially available lignin sulphonate and then the mixture is sprayed dry to an ultrafine powder having an average particle size of 1.mu. and a coupage ratio of 3.5:10.
12 parts of this ultra fine powder are dispersed in 100 parts of water and this is added at 60.degree. C. to 13,000 parts of a circulating liquor (containing 30 parts of ammonium sulphate and 0.3 parts of formic acid as a buffer and optionally a carrier-/levelling agent combination).
In a dyeing autoclave with a precleaned pressed cross spool of 1000 parts of polyester yarn on a plastic holder the circulating liquor is then heated to 130.degree. C. over 35 minutes. After 90 minutes at 130.degree. C., the autoclave is cooled to 80.degree. C. and the exhausted liquor is drained off. The resulting dyed substrate is washed thoroughly with cold water and then reductively cleared according to known art standard methods and finally dried. A level, deep ruby red colour results.
The Application Example can be repeated using, instead of the dyestuff of Example 1, an appropriate amount of any one of Examples 2 to 504.

Claims

1. A compound of the formula I ##STR177## in which D is a diazo component;
K is an aromatic group of the formula a, b or c ##STR178## where R is a group of the formula --CH(R.sub.4)--CO--O--R.sub.5, --CH.sub.2 CF.sub.3 or --CH.sub.2 CF.sub.2 CF.sub.2 H;
R.sub.6 is hydrogen or hydroxy,
R.sub.1 is hydrogen, chloro, C.sub.1-4 alkyl, C.sub.1-4 alkoxy or acylamino,
R.sub.2 is hydrogen, C.sub.1-4 alkoxy, C.sub.1-4 alkoxyethoxy, chloro, bromo and
R.sub.3 is selected from hydrogen, C.sub.1-6 alkyl, C.sub.3-4 alkenyl, chloroC.sub.3-4 alkenyl, bromoC.sub.3-4 alkenyl, C.sub.3-4 alkynyl, phenyl-C.sub.1-4 alkyl, C.sub.1-4 alkoxycarbonyl-C.sub.1-4 alkyl, C.sub.3-4 alkenyloxycarbonyl-C.sub.1-4 alkyl, C.sub.3-4 alkynyloxycarbonyl-C.sub.1-4 alkyl, phenoxy-C.sub.2-4 alkyl, --CH.sub.2 --CH(R.sub.8)CH.sub.2 --R.sub.9 and C.sub.2-4 alkyl substituted by 1 to 3 groups selected from halogen, cyano, C.sub.1-4 alkoxy, C.sub.1-4 alkylcarbonyloxy and C.sub.1-4 alkoxycarbonyloxy;
or R.sub.2 together with R.sub.3 in the group a) form a group of the formula-*CH(CH.sub.3)CH.sub.2 C(CH.sub.3).sub.2 where the * carbon atom is attached to the group a);
R.sub.4 is hydrogen, phenyl or C.sub.1-4 alkyl,
R.sub.5 is phenyl, unsubstituted or substituted by one to three groups selected from halogen, C.sub.1-4 alkyl, C.sub.1-4 alkoxycarbonyl and C.sub.1-4 alkoxy or phenyl substituted by one group selected from formyl, cyan, rhodan, phenyl, benzyloxy, C.sub.1-4 alkoxycarbonyl-C.sub.1-2 alkoxy, C.sub.1-4 alkylcarbonylamino, C.sub.1-4 alkylcarbonyloxy and nitro; alpha or beta naphthyl, phenyl-C.sub.1-4 alkyl or 1-phenyl-propenyl-3, in which the phenyl group (in phenyl C.sub.1-4 alkyl and 1-phenyl propenyl-3) is unsubstituted or substituted by one or two substituents selected from halogen, C.sub.1-4 alkyl and C.sub.1-4 alkoxy or by one nitro or C.sub.1-4 alkoxycarbonyl group; or
R.sub.5 is allyl, haloallyl, methallyl, propargyl, tetrahydrofuryl-2-methyl, tetrahydropyranyl-2-methyl, chlor-C.sub.2-4 alkyl, bromoC.sub.2-4 alkyl or a group of the formula ##STR179## R.sub.7 is hydrogen or C.sub.1-4 alkyl; R.sub.8 is hydroxy, C.sub.1-4 alkylcarbonyloxy or C.sub.1-4 alkoxycarbonyloxy;
R.sub.9 is chloro, C.sub.1-4 alkoxy, phenoxy, allyloxy or C.sub.1-4 alkylcarbonyloxy;
R.sub.10 is hydrogen or C.sub.1-4 alkyl;
R.sub.11 is hydrogen, halogen, C.sub.1-4 alkyl, C.sub.1-4 alkoxy or nitro
Y is C.sub.2-3 alkylene and
n is 0 or 1;
with the proviso that when K is a group of formula b) or c), then R.sub.3 is hydrogen (and mixtures containing compounds of formula I).
2. A compound according to claim 1 in which D is a diazo component of the phenyl, thienyl, thiazolyl, isothiazolyl, thiadiazolyl, pyrazolyl, imidazolyl, triazolyl, benzthiazolyl, or benzisothiazolyl series.
3. A compound according to claim 1 in which D is D.sub.1 where D.sub.1 is a compound of formula 1 to 11 below ##STR180## in which R.sub.20 is hydrogen, chloro, bromo, cyano, nitro-, C.sub.1-4 alkoxy carbonyl, C.sub.1-4 alkylsulphonyl;
R.sub.21 is chloro, bromo, nitro, C.sub.1-4 alkyl, C.sub.1-4 alkylsulfonyl, C.sub.1-4 alkylcarbonyl, aminosulfonyl, mono- or di-C.sub.1-4 alkylaminosulfonyl, phenylaminosulfonyl, C.sub.1-4 alkoxycarbonyl, aminocarbonyl, mono- or di-C.sub.1-4 -alkylaminocarbonyl, phenylaminocarbonyl, phenylazo, benzyloxycarbonyl, tetrahydro-furfuryl-2-oxycarbonyl, C.sub.3-4 alkenyloxycarbonyl or C.sub.3-4 alkinyloxycarbonyl;
R.sub.22 is hydrogen, chloro, bromo or cyano;
R.sub.23 is hydrogen or chloro, or when R.sub.22 is hydrogen, R.sub.23 is additionally rhodan;
R.sub.24 is nitro, C.sub.1-4 alkylcarbonyl, C.sub.1-4 alkoxycarbonyl, cyano, aminocarbonyl, mono- or di-C.sub.1-2 alkylaminocarbonyl;
R.sub.25 is hydrogen chloro, bromo, C.sub.1-4 alkyl or phenyl;
R.sub.26 is nitro, cyano, formyl, dicyanovinyl or a group of the formula --CH.dbd.CH--NO.sub.2, --CH.dbd.C(CN)CO--OC.sub.1-4 -alkyl, H.sub.5 C.sub.6 --N.dbd.N-- or 3- or 4--NO.sub.2 --C.sub.6 H.sub.4 --N.dbd.N--;
R.sub.27 is cyano or C.sub.1-4 alkoxycarbonyl;
R.sub.28 is C.sub.1-4 alkyl or phenyl;
R.sub.29 is --CN, --CH.dbd.CH.sub.2 or phenyl;
R.sub.30 is C.sub.1-4 alkyl;
R.sub.31 is hydrogen, chloro, bromo, cyano, rhodan, nitro, C.sub.1-4 alkoxycarbonyl or di-C.sub.1-4 alkylaminosulfonyl;
R.sub.32 is hydrogen chloro or bromo; and
R.sub.33 is C.sub.1-4 alkyl, C.sub.1-4 alkoxycarbonyl-C.sub.1-4 alkylene or --C.sub.1-4 alkylene-COOCH.sub.2 CF.sub.3
in which any phenyl group present in R.sub.20 to R.sub.30 is unsubstituted or substituted by one or two groups selected from chloro, bromo, methyl, ethyl, methoxy and ethoxy.
4. A compound according to claim 1 in which K is K.sub.1 where K.sub.1 is a group of formula a) defined above.
5. A compound according to claim 1 in which R is R' where R' is --CH(R.sub.4 ')--CO--O--R.sub.5 ' or --CH.sub.2 CF.sub.3 where R.sub.4 ' is selected from hydrogen and C.sub.1-2 alkyl and R.sub.5 ' is phenyl, unsubstituted or substituted by one or two substituents selected from chloro, C.sub.1-2 alkyl, C.sub.1-2 alkoxy and one phenyl; phenyl C.sub.1-2 alkyl, phenoxy ethyl or 1-phenylpropenyl-3, the phenyl group of each of the last three substituents (phenyl C.sub.1-2 alkyl, phenoxy ethyl or 1-phenylpropenyl-3) being unsubstituted or substituted by one or two groups selected from chloro, methyl and C.sub.1-2 alkoxy or one group nitro) or R.sub.5 ' is alpha and beta naphthyl.
6. A compound according to claim 1 in which R.sub.1 is R.sub.1 ' where R.sub.1 ' is selected from hydrogen, C.sub.1-2 alkyl, chloro and acylamino.
7. A compound according to claim 1 in which R.sub.2 is R.sub.2 ' where R.sub.2 ' is selected from hydrogen, chloro, C.sub.1-2 alkoxy, C.sub.1-2 alkoxyethoxy or R.sub.2 ' (when in formula a) together with R.sub.3 forms the group --CH(CH.sub.3)CH.sub.2 C(CH.sub.3).sub.2.
8. A compound according to claim 1 in which R.sub.3 is R.sub.3 ' where R.sub.3 ' is selected from hydrogen, C.sub.1-4 alkyl, cyanoethyl, C.sub.1-2 alkoxyethyl, C.sub.3-4 alkenyl, chloroallyl, C.sub.3-4 alkynyl, C.sub.1-2 alkoxycarbonylmethyl, allyloxycarbonylmethyl or propargyloxycarbonylmethyl.
9. A compound according to claim 1 in which R.sub.4 is R.sub.4 ' where R.sub.4 ' is selected from hydrogen and C.sub.1-2 alkyl.
10. A compound according to claim 1 in which R.sub.5 is R.sub.5 ' where R.sub.5 ' is phenyl, unsubstituted or substituted by one or two substituents selected from chloro, C.sub.1-2 alkyl, C.sub.1-2 alkoxy and one phenyl; phenyl C.sub.1-2 alkyl, phenoxy ethyl or 1-phenylpropenyl-3, the phenyl group of each of the last three substituents (phenyl C.sub.1-2 alkyl, phenoxy ethyl or 1-phenylpropenyl-3) being unsubstituted or substituted by one or two groups selected from chloro, methyl and C.sub.1-2 alkoxy or one group nitro) or R.sub.5 ' is alpha and beta naphthyl.
11. A compound according to claim 1 in which Y is Y' where Y' is a group of the formula
--CH.sub.2 CH.sub.2 -- or --CH.sub.2 CH(CH.sub.3)--.
12. A compound according to claim 1 in which D is D.sub.2 where D.sub.2 is a diazo component of the 2,6-dicyano-4-chlorophenyl,2,6-dicyano-4-bromo-phenyl,2,6-dicyano-4-methylphenyl, 2,6-dicyano-4-nitrophenyl 2,4-dinitro-6-chlorophenyl, 2,4-dinitro-6-bromophenyl, 2,4-dinitro-6-cyanophenyl, 2-chloro- or 2-bromo-4-nitro-6-cyanophenyl, 2,4-dinitrophenyl, 2,6-dichloro- or 2,6-dibromo-4-nitrophenyl, 2-chloro-4-nitro-6-bromophenyl, 2-chloro- or 2-cyano-4-nitro-phenyl, 2,4-dinitro-5-chlorophenyl, 2,4-dinitro-5,6-dichlorophenyl, 2,5-dichloro-4-nitro-phenyl, 4-nitrophenyl, 4-phenylazophenyl, 4-C.sub.1-4 alkoxy-carbonylphenyl, 2-C.sub.1-4 alkoxycarbonyl-4-nitrophenyl, 4-benzyloxycarbonylphenyl, 4-(tetrahydro-furfuryl-2'-oxycarbonyl)-phenyl, 3,5-dicyano-4-chlorothienyl-2,3,5-dicyanothienyl-2,3-cyano-5-nitro-thienyl-2,3-acetyl-5-nitro-thienyl-2,3,5-dinitrothienyl-2,3-(C.sub.1-4 alkoxycarbonyl)-5-nitro-thienyl-.sub.2,5 -phenylazo-3-cyano-thienyl-2,5-phenylazo-3-cyano-4-methyl-thienyl-2,5-nitro-thiazolyl-2,5-nitrobenziso-thiazolyl-3,3-methyl-4-cyano-isothiazolyl-5,3-Phenyl-1,2,4-thiadiazolyl-2,5-(C.sub.1-2 alkylmercapto)-1,3,4-thiadiazolyl-2,3-C.sub.1-4 alkoxycarbonylethylmercapto-1,2,4-thiadiazolyl-5,1-cyano-methyl-4,5-dicyano-imidazolyl-2,6-nitrobenzthiazolyl-2,5-nitrobenzthiazolyl-2,6-rhodanbenzthiazolyl-2,6-chlorobenzthiazolyl-2,(5),6,(7)-dichlorobenzthiazolyl-2, or a group of the formula ##STR181## where R.sub.35 is oxygen or a group of the formula ##STR182##
13. A compound according to claim 1 in which the compounds of formula I are of formula Ia ##STR183## in which D.sub.1 is a compound of formula 1 to 11 below ##STR184## in which R.sub.20 is hydrogen, chloro, bromo, cyano, nitro-, C.sub.1-4 alkoxy carbonyl, C.sub.1-4 alkylsulphonyl;
R.sub.21 is chloro, bromo, nitro, C.sub.1-4 alkyl, C.sub.1-4 alkylsulfonyl, C.sub.1-4 alkylcarbonyl, aminosulfonyl, mono- or di-C.sub.1-4 alkylaminosulfonyl, phenylaminosulfonyl, C.sub.1-4 alkoxycarbonyl, aminocarbonyl, mono- or di-C.sub.1-4 -alkylaminocarbonyl, phenylaminocarbonyl, phenylazo, benzyloxycarbonyl, tetrahydro-furfuryl-2-oxycarbonyl, C.sub.3-4 alkenyloxycarbonyl or C.sub.3-4 alkinyloxycarbonyl;
R.sub.22 is hydrogen, chloro, bromo or cyano;
R.sub.23 is hydrogen or chloro, or when R.sub.22 is hydrogen, R.sub.23 is additionally rhodan;
R.sub.24 is nitro, C.sub.1-4 alkylcarbonyl, C.sub.1-4 alkoxycarbonyl, cyano, aminocarbonyl, mono- or di-C.sub.1-2 alkylaminocarbonyl;
R.sub.25 is hydrogen, chloro, bromo, C.sub.1-4 alkyl or phenyl;
R.sub.26 is nitro, cyano, formyl, dicyanovinyl or a group of the formula --CH.dbd.CH--NO.sub.2, --CH.dbd.C(CN)CO--OC.sub.1-4 -alkyl, H.sub.5 C.sub.6 --N.dbd.N-- or 3- or 4-NO.sub.2 --C.sub.6 H.sub.4 --N.dbd.N--;
R.sub.27 is cyano or C.sub.1-4 alkoxycarbonyl;
R.sub.28 is C.sub.1-4 alkyl or phenyl;
R.sub.29 is --CN, --CH.dbd.CH.sub.2 or phenyl;
R.sub.30 is C.sub.1-4 alkyl;
R.sub.31 is hydrogen, chloro, bromo, cyano, rhodan, nitro, C.sub.1-4 alkoxycarbonyl or
di-C.sub.1-4 alkylaminosulfonyl;
R.sub.32 is hydrogen chloro or bromo; and
R.sub.33 is C.sub.1-4 alkyl, C.sub.1-4 alkoxycarbonyl-C.sub.1-4 alkylene or --C.sub.1-4 alkylene-COOCH.sub.2 CF.sub.3
in which any phenyl group present in R.sub.20 to R.sub.30 is unsubstituted or substituted by one or two groups selected from chloro, bromo, methyl, ethyl, methoxy and ethoxy;
R.sub.1 ' where R.sub.1 ' is selected from hydrogen, C.sub.1-2 alkyl, chloro and acylamino;
R.sub.2 ' where R.sub.2 ' is selected from hydrogen, chloro, C.sub.1-2 alkoxy, C.sub.1-2 alkoxyethoxy or R.sub.2 ' (when in formula a) together with R.sub.3 forms the group --CH(CH.sub.3)CH.sub.2 C(CH.sub.3).sub.2 ;
Y' where Y' is a group of the formula --CH.sub.2 CH.sub.2 -- or --CH.sub.2 CH(CH.sub.3)--;
R.sub.4 ' where R.sub.4 ' is selected from hydrogen and C.sub.1-2 alkyl; and
R.sub.3 and R.sub.5 are as defined in claim 1.
14. A compound according to claim 1 in which the compounds of formula I are of formula Ib ##STR185## in which D.sub.2 is is a diazo component of the 2,6-dicyano-4-chlorophenyl, 2,6-dicyano-4-bromophenyl, 2,6-dicyano-4-methylphenyl, 2,6-dicyano-4-nitrophenyl,2,4-dinitro-6-chlorophenyl, 2,4-dinitro-6-bromophenyl, 2,4-dinitro-6-cyanophenyl, 2-chloro- or 2-bromo-4-nitro-6-cyanophenyl, 2,4-dinitrophenyl, 2,6-dichloro- or 2,6-dibromo-4-nitrophenyl, 2-chloro-4-nitro-6-bromophenyl, 2-chloro- or 2-cyano-4-nitrophenyl, 2,4-dinitro-5-chlorophenyl,2,4-dinitro-5,6-dichlorophenyl,2,5-dichloro-4-nitro-phenyl,4-nitrophenyl, 4-phenylazophenyl, 4-C.sub.1-4 alkoxy-carbonyl-phenyl, 2-C.sub.1-4 alkoxycarbonyl-4-nitrophenyl, 4-benzyloxycarbonylphenyl, 4-(tetrahydro-furfuryl-2'-oxy-carbonyl)-phenyl, 3,5-dicyano-4-chlorothienyl-2,3,5-dicyanothienyl-2,3-cyano-5-nitro-thienyl-2,3-acetyl-5-nitrothienyl-2,3,5-dinitrothienyl-2,3-(C.sub.1-4 alkoxycarbonyl)-5-nitro-thienyl-2,5-phenylazo-3-cyanothienyl-2,5-phenylazo-3-cyano-4-methyl-thienyl-2,5-nitro-thiazolyl-2,5-nitro-benzisothiazolyl-3,3-methyl-4-cyano-isothiazolyl-5,3-Phenyl-1,2,4-thiadiazolyl-2,5-(C.sub.1-2 alkylmercapto)-1,3,4-thiadiazolyl-2,3-C.sub.1-4 alkoxycarbonylethylmercapto-1,2,4-thiadiazolyl-5,1-cyanomethyl-4,5-dicyano-imidazolyl-2,6-nitrobenzthiazolyl-2,5-nitrobenzthiazolyl-2,6-rhodan-benzthiazolyl-2,6-chlorobenzthiazolyl-2, ( 5),6,(7)-dichloro-benz-thiazolyl-2, or a group of the formula ##STR186## where R.sub.35 is oxygen or a group of the formula ##STR187## R.sub.1 ' where R.sub.1 ' is selected from hydrogen, C.sub.1-2 alkyl, chloro and acylamino;
R.sub.2 ' where R.sub.2 ' is selected from hydrogen, chloro, C.sub.1-2 alkoxy, C.sub.1-2 alkoxyethoxy or R.sub.2 ' (when in formula a) together with R.sub.3 forms the group --CH(CH.sub.3)CH.sub.2 C(CH.sub.3).sub.2 ;
Y' where Y' is a group of the formula --CH.sub.2 CH.sub.2 -- or --CH.sub.2 CH(CH.sub.3)--;
R.sub.4 ' where R.sub.4 ' is selected from hydrogen and C.sub.1-2 alkyl;
and R.sub.3 and R.sub.5 are as defined in claim 1.
15. A compound according to claim 1 in which the compounds of formula I are those of formula Ic ##STR188## in which D.sub.3 is a diazo component of the 2,4-dinitro-6-chlorophenyl, 2,4-dinitro-6-bromophenyl, 2,4-dinitro-6-cyanophenyl, 2,4-dinitro-5-chlorophenyl or 2,4-dinitro-5-rhodanphenyl, 2,4-dinitro-5,6-dichlorophenyl series;
R' is --CH(R.sub.4 ')--CO--O--R.sub.5 ' or CH.sub.2 CF.sub.3 where R.sub.4 ' and R.sub.5 ' are defined below;
R.sub.1 " is acylamino;
R.sub.2 " is C.sub.1-2 alkoxy or C.sub.1-2 alkoxyethoxy,
R.sub.3 ' is selected from hydrogen, C.sub.1-4 alkyl, cyanoethyl, C.sub.1-2 alkoxyethyl, C.sub.3-4 alkenyl, chloroC.sub.3-4 alkenyl, C.sub.3-4 alkynyl, C.sub.1-2 alkoxycarbonylmethyl, allyloxycarbonylmethyl, or propargyl-oxycarbonylmethyl;
R.sub.4 ' is selected from hydrogen and C.sub.1-2 alkyl;
R.sub.5 ' is phenyl, unsubstituted or substituted by one or two substituents selected from chloro, C.sub.1-2 alkyl, C.sub.1-2 alkoxy and phenyl; phenyl C.sub.1-2 alkyl, phenoxy ethyl or 1-phenylpropenyl-3, (the phenyl group of each of the last three substituents (phenyl C.sub.1-2 alkyl, phenoxy ethyl or 1-phenylpropenyl-3) being unsubstituted or substituted by one or two groups selected from chloro, methyl and C.sub.1-2 alkoxy or one group nitro) or R.sub.5 ' is alpha and beta naphthyl; and
Y is Y' where Y' is a group of the formula --CH.sub.2 CH.sub.2 -- or --CH.sub.2 CH(CH.sub.3)--.
16. A compound according to claim 15 in which the compounds of formula Ic are those in which
D.sub.3 is D.sub.3 ' where D.sub.3 ' is a diazo component of the 2,4-dinitro-6-chlorophenyl or 2,4-dinitro-6-bromophenyl series;
R.sub.1 " is --NH--COC.sub.1-2 alkyl;
R.sub.2 " is R.sub.2 '" where R.sub.2 '" is C.sub.1-2 alkoxy;
R.sub.3 ' is R.sub.3a where R.sub.3a is hydrogen, allyl, chloroallyl or propargyl;
R.sub.5 ' is R.sub.5 " where R.sub.5 " is phenyl, phenoxyethyl or benzyl, in which the phenyl group of each substituent is unsubstituted or substituted by one or two groups selected from chloro, methyl and C.sub.1-2 alkoxy or one group nitro;
R' is R'" where R'" is a group of the formula --CH.sub.2 CO--O--R.sub.5 ", where R.sub.5 " is defined above; and
Y is Y" where Y" is 1,2 ethylene.
17. A compound according to claim 1 in which the compounds of formula I are those of formula Id ##STR189## in which D.sub.4 is a diazo component of the 4-nitrophenyl, 2-chloro-4-nitrophenyl, 2,6-dichloro-4-nitrophenyl, 2-chloro-4-nitro-6-bromophenyl or 2-cyano-4-nitrophenyl series; R.sub.1a is hydrogen, methyl, acylamino or chloro;
R.sub.b is a group of the formula --CH(R.sub.4 ')--CO--O--R.sub.5 ', where R.sub.4 ' is selected from hydrogen and C.sub.1-2 alkyl and R.sub.5 ' is phenyl, unsubstituted or substituted by one or two substituents selected from chloro, C.sub.1-2 alkyl, C.sub.1-2 alkoxy and phenyl; phenyl C.sub.1-2 alkyl or 1-phenylpropenyl-3 (the phenyl group of each of the last two substituents (phenyl C.sub.1-2 alkyl or 1-phenylpropenyl-3) being unsubstituted or substituted by one or two groups selected from chloro, methyl and C.sub.1-2 alkoxy or one group nitro or R.sub.5 ' is alpha and beta naphthyl;
R.sub.3b is C.sub.1-4 alkyl, cyano-C.sub.1-4 alkyl, C.sub.1-4 alkoxyethyl, --C.sub.2 H.sub.4 --O--CO--C.sub.1-4 alkyl, --C.sub.2 H.sub.4 --O--CO--OC.sub.1-4 alkyl or benzyl;
R.sub.4 ' is selected from hydrogen and C.sub.1-2 alkyl;
R.sub.5 ' is phenyl, unsubstituted or substituted by one or two substituents selected from chloro, C.sub.1-2 alkyl, C.sub.1-2 alkoxy and phenyl; phenyl C.sub.1-2 alkyl, or 1-phenylpropenyl-3 (the phenyl group of each of the last two substituents (phenyl C.sub.1-2 alkyl or 1-phenylpropenyl-3) being unsubstituted or substituted by one or two groups selected from chloro, methyl and C.sub.1-2 alkoxy or one group nitro or R.sub.5 ' is alpha and beta naphthyl; and
Y' is a group of the formula --CH.sub.2 CH.sub.2 -- or --CH.sub.2 CH(CH.sub.3)--.
18. A compound according to claim 17 in which the compounds of formula Id are those in which D.sub.4 is D.sub.5 where D.sub.5 is 2,6-dichloro-4-nitrophenyl or 2-cyano-4-nitrophenyl and R.sub.1a is hydrogen, R.sub.3b is C.sub.1-4 alkyl, R.sub.4 ' is hydrogen and Y' is --CH.sub.2 CH.sub.2 --.
19. A process for dyeing a substrate comprising applying to the substrate a compound of claim 1.
20. A process for preparing a compound according to claim 1 comprising coupling one mole of a diazotized amine of formula II
D--NH.sub.2 (II)
with one mole of a compound of formula III
H--K--N(R.sub.3)--Y--CO--O--R (III)
where the symbols are as defined in claim 1.

Priority Claims (3)

Number	Date	Country
42 35 137.5	Oct 1992	DEX
42 37 465.0	Nov 1992	DEX
43 20 773.1	Jun 1993	DEX

US Referenced Citations (3)

Number	Name	Date
5055567	Liechti et al.	Oct 1991
5116958	Liechti et al.	May 1992
5298610	Hahn et al.	Mar 1994

Disperse dyes

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Priority Claims (3)

US Referenced Citations (3)