CH646973A5 - Process for the preparation of novel 5-aroyl-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acids - Google Patents
Process for the preparation of novel 5-aroyl-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acids Download PDFInfo
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- CH646973A5 CH646973A5 CH86684A CH86684A CH646973A5 CH 646973 A5 CH646973 A5 CH 646973A5 CH 86684 A CH86684 A CH 86684A CH 86684 A CH86684 A CH 86684A CH 646973 A5 CH646973 A5 CH 646973A5
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- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
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- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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Abstract
Description
1 1
2 2nd
Gegenstand der Erfindung ist ein Verfahren zum Färben oder Bedrucken von Textilfasern aus Homo- oder Mischpolymerisaten des Acrylnitrils oder as.Dicyanäthylens oder aus sauer modifizierten synthetischen Polymeren, gekennzeichnet durch die Verwendung neuer kationischer Farbstoffe der allgemeinen Formel The invention relates to a process for dyeing or printing textile fibers from homo- or copolymers of acrylonitrile or as.Dicyanäthylenes or from acid-modified synthetic polymers, characterized by the use of new cationic dyes of the general formula
3© 3 ©
-ç-h=N^>N -ç-h = N ^> N
(R4)m (R4) m
I I.
R R
/r6 / r6
<v» <v »
An At
(-) (-)
worin wherein
R Wasserstoff oder einen Alkyl-, Cycloalkyl-, Aralkyl-, Aryl- oder heterocyclischen Rest; R is hydrogen or an alkyl, cycloalkyl, aralkyl, aryl or heterocyclic radical;
Ri einen Alkyl- oder Arylrest und Ri is an alkyl or aryl radical and
R2 einen Alkyl- oder Arylrest bedeuten oder R, und R2 zusammen eine Tri- oder Tetramethylenbrücke bilden; R2 is an alkyl or aryl radical or R, and R2 together form a tri- or tetramethylene bridge;
R3 einen Alkyl-, Alkenyl- oder Aralkylrest; R3 is an alkyl, alkenyl or aralkyl radical;
R4, R5 nichtionische Substituenten; R4, R5 nonionic substituents;
R6 Wasserstoff, einen Alkyl-, Cycloalkyl- oder Aralkylrest; R6 is hydrogen, an alkyl, cycloalkyl or aralkyl radical;
15 m die Zahlen 0, 1 oder 2, 15 m the numbers 0, 1 or 2,
n die Zahl 1 oder 2 und An'"1 ein Anion bedeuten, n is the number 1 or 2 and An '"1 is an anion,
und worin die genannten cyclischen und acyclischen Reste durch nichtionische Reste und/oder die Carboxylgruppe sub-20 stituiert sein können. and wherein said cyclic and acyclic radicals can be sub-20 substituted by nonionic radicals and / or the carboxyl group.
Hervorzuheben sind Farbstoffe der allgemeinen Formel Dyes of the general formula should be emphasized
R« -N* * 10 © R «-N * * 10 ©
R, R,
N=N N = N
<0H2>n ~Qf' <0H2> n ~ Qf '
'14 '14
An At
(-) (-)
II II
worin wherein
R7 Wasserstoff, einen C,-C4-Alkyl-, einen 5- oder 6glie-drigen cycloaliphatischen oder einen 5- oder ógliedrigen O, N und/oder S enthaltenden heterocyclischen Rest; 40 R7 is hydrogen, a C, -C4-alkyl, a 5- or 6-membered cycloaliphatic or a 5- or O-membered O, N and / or S-containing heterocyclic radical; 40
Rs einen C,-C4-Alkyl- oder Phenylrest; Rs is a C, -C4 alkyl or phenyl radical;
R9 einen C]—C4-Alkyl- oder Phenylrest bedeuten oder R8 und R9 zu einer Tri- oder Tetramethylenbrücke verbunden sind; R9 represents a C] —C4-alkyl or phenyl radical or R8 and R9 are connected to form a tri- or tetramethylene bridge;
Rio einen C,-C4-Alkylrest, Benzyl, /3-Hydroxyäthyl, 45 /3-Cyanäthyl,y3-Carboxyäthyl, Methoxy- bzw. Athoxy-methyl, /S-Methoxy- bzw./3-Äthoxyäthyl, Methoxy- bzw. Äthoxy-carbonyl-methyl, /8-Methoxy- bzw. j3-Äthoxycarbonyl-äthyl, Aminocarbonyl-methyl, Aminocarbonyl-äthyl ; Rio a C, -C4-alkyl radical, benzyl, / 3-hydroxyethyl, 45/3-cyanoethyl, y3-carboxyethyl, methoxy- or athoxy-methyl, / S-methoxy- or / 3-ethoxyethyl, methoxy- or Ethoxy-carbonyl-methyl, / 8-methoxy- or j3-ethoxycarbonyl-ethyl, aminocarbonyl-methyl, aminocarbonyl-ethyl;
Ru, R,2 unabhängig voneinander Wasserstoff, einen Ci—C4- so Alkyl- oder Ci-C4-Alkoxyrest, einen Formyl-, Acetyl-, Pro-pionyl-, Butyryl-, Hydroxyacetyl-, Methoxyacetyl-, Cyan-acetyl-, ß- oder j/-Hydroxypropionyl-, Benzoyl-, o-, p- oder m-Chlorbenzoyl-, o-, p- oder m-Methylbenzoyl-, o-, p- oder m-Trifluormethylbenzoyl-, o-, p- oder m-Hydroxybenzoyl-, . 55 o-, p- oder m-Nitrobenzoyl-, Phenacetyl-, Phenoxyacetyl-, Thenoyl-, Pyridoyl-, Acetoacetyl-, Aminocarbonyl-, Dimethyl-aminocarbonyl-, Methylaminocarbonyl- oder Phenylamino-carbonyl-aminorest oder Halogen; Ru, R, 2 independently of one another are hydrogen, a C 1 -C 4 -alkyl or C 1 -C 4 -alkoxy radical, a formyl, acetyl, propionyl, butyryl, hydroxyacetyl, methoxyacetyl, cyanoacetyl, ß- or j / -hydroxypropionyl-, benzoyl-, o-, p- or m-chlorobenzoyl-, o-, p- or m-methylbenzoyl-, o-, p- or m-trifluoromethylbenzoyl-, o-, p- or m-hydroxybenzoyl-. 55 o-, p- or m-nitrobenzoyl, phenacetyl, phenoxyacetyl, thenoyl, pyridoyl, acetoacetyl, aminocarbonyl, dimethylaminocarbonyl, methylaminocarbonyl or phenylamino-carbonyl-amino radical or halogen;
Ri3 Wasserstoff, einen Ci—C4-Alkylrest, /3-Hydroxyäthyl, /3-Methoxy-carbonyläthyl, /8-Athoxycarbonyläthyl, y3-Cyan-äthyl, /ï-Formyloxyathyl, /3-Acetoxyäthyl, /J-Propionyloxy-äthyl, /3-Methoxycarbonyloxyäthyl, y3-Äthoxycarbonyloxy-äthyl, /3-Methoxyäthyl, /3-Äthoxyäthyl, /3-Phenoxyäthyl, /3-Phenoxyactoxyäthyl, /3-Acetylaminoäthyl, /3-Propionyl-aminoäthyl, /3-Formylaminoäthyl, y-Formylaminopropyl, y-Acetylaminopropyl, y-Propionylaminopropyl, ß-C hloräthyl, y-Chlorpropyl, ^-Ureidoäthyl, /3-Methylureidoäthyl, ß-D\-methylureidoäthyl, /3-Phenylureidoäthyl, /3-Methylamino-carbonyloxyäthyl, /3-Phenylaminocarbonyloxyäthyl, ß-Di-methylaminocarbonyloxyäthyl, /3-Dimethylaminoäthyl, ß-Di-äthylaminoäthyl, y-Dimethylaminopropyl, y-Diäthylamino-propyl, /3-Methyl- bzw. /i-Phenylsuifonyläthyl, Cyclohexyl, Benzyl oder Phenäthyl; Ri3 is hydrogen, a C 1 -C 4 -alkyl radical, / 3-hydroxyethyl, / 3-methoxycarbonylethyl, / 8-ethoxycarbonylethyl, y3-cyanoethyl, / ï-formyloxyathyl, / 3-acetoxyethyl, / J-propionyloxyethyl, / 3-methoxycarbonyloxyethyl, y3-ethoxycarbonyloxyethyl, / 3-methoxyethyl, / 3-ethoxyethyl, / 3-phenoxyethyl, / 3-phenoxyactoxyethyl, / 3-acetylaminoethyl, / 3-propionylaminoethyl, / 3-formylaminoethyl, y- Formylaminopropyl, y-acetylaminopropyl, y-propionylaminopropyl, ß-chloroethyl, y-chloropropyl, ^-ureidoethyl, / 3-methylureidoethyl, ß-D \ -methylureidoethyl, / 3-phenylureidoethyl, / 3-methylamino-carbonyloxyethyl, / 3- Phenylaminocarbonyloxyethyl, ß-dimethylaminocarbonyloxyethyl, / 3-dimethylaminoethyl, ß-di-ethylaminoethyl, y-dimethylaminopropyl, y-diethylamino-propyl, / 3-methyl- or / i-phenylsuifonylethyl, cyclohexyl, benzyl or phenethyl;
R14 Wasserstoff, einen Ct-C4-Alkyl-, Ci-C4-Alkoxyrest, Nitro oder Halogen; R14 is hydrogen, a Ct-C4-alkyl, Ci-C4-alkoxy radical, nitro or halogen;
n die Zahl 1 oder 2 und An(_) ein Anion bedeuten. n is the number 1 or 2 and An (_) is an anion.
Bevorzugte Farbstoffe sind solche der allgemeinen Formel Preferred dyes are those of the general formula
3 3rd
4 4th
worin R7, R8, R9, R10, R13 und An( 1 die oben angegebene Bedeutung haben, Ri5 für Wasserstoff, Methyl, Formyl-, wherein R7, R8, R9, R10, R13 and An (1 have the meaning given above, Ri5 for hydrogen, methyl, formyl,
Acetyl-, Propionyl- oder Benzoylamino und n für 1 oder 2 stehen. Acetyl-, propionyl- or benzoylamino and n are 1 or 2.
Besonders bevorzugte Farbstoffe sind solche der Formel 5 Particularly preferred dyes are those of the formula 5
IV IV
ch2-<3 ch2- <3
An At
(-) (-)
R16 Methyl, lsopropyl,/?-Cyanäthyl,/3-Hydroxyäthyl, Sulfolanyl-(3), Pyridyl-(2), Benzthiazolyl-(2), Thiazolyl-(2), Phenyl, 4-Chlorphenyl, 2-Chlorphenyl, 4-Methylphenyl, 2-Methylphenyl, Cyclohexyl, Benzyl; R16 methyl, isopropyl, /? - cyanoethyl, / 3-hydroxyethyl, sulfolanyl- (3), pyridyl- (2), benzothiazolyl- (2), thiazolyl- (2), phenyl, 4-chlorophenyl, 2-chlorophenyl, 4 -Methylphenyl, 2-methylphenyl, cyclohexyl, benzyl;
Rl7, R,s je Methyl oder gemeinsam Tetramethylen; Rl7, R, s each methyl or together tetramethylene;
R]9 Methyl, Äthyl oder Benzyl; R] 9 methyl, ethyl or benzyl;
R20 Wasserstoff, Methyl, Formyl-, Acetyl- oder Benzoylamino; R20 is hydrogen, methyl, formyl, acetyl or benzoylamino;
R21 C|-C4-Alkyl, ß-Cyanäthyl, /?-Hydroxyäthyl, /3-Chlor-äthyl, /3-Phenoxyäthyl oder Benzyl und R21 C | -C4-alkyl, ß-cyanoethyl, /? - hydroxyethyl, / 3-chloroethyl, / 3-phenoxyethyl or benzyl and
An«1 C1M. BrM. C^SO,'-', C2H5S04<', At «1 C1M. BrM. C ^ SO, '-', C2H5S04 <',
{3"S0V H3C0^°3H {3 "S0V H3C0 ^ ° 3H
oder ZnCl3(_) bedeuten. or ZnCl3 (_) mean.
Nichtionische Substituenten im Sinne der vorliegenden Erfindung sind die in der Farbstoffchemie üblichen nicht-dissoziierenden Substituenten wie Halogen, Alkyl, Aralkyl, Alkenyl, Aryl, Hydroxy, Alkoxy, Aralkoxy, Aryloxy, Alkyl-thio, Aralkylthio, Arylthio, Nitro, Cyan, Alkoxycarbonyl, Formyl, Alkylcarbonyl, Arylcarbonyl, Aralkylcarbonyl, Alk-oxycarbonyloxy, Alkylcarbonylamino, Arylcarbonylamino, Alkylsulfonylamino, Arylsulfonylamino, Ureido, N-Aryl- oder N-Alkyl-ureido, Aryloxycarbonylamino, Alkyloxycarbonyl-amino, Carbamoyl, N-Alkyl-carbamoyl, N,N-Dialkylcarba-moyl, N-Alkyl-N-aryl-carbamoyl, Sulfamoyl, N-Alkylsulfo-moyl, N.N-Dialkyl-sulfamoyl, Carbonsäurealkylester-, Carbon-säurearylester-, Sulfonsäurealkylester- oder Sulfonsäurearyl-ester-Gruppen, wobei in den genannten Alkylresten vorzugsweise 1-4 C-Atome vorliegen, und die Arylgruppen vorzugsweise der Phenyl- oder Naphthalinreihe angehören, sowie Reste der heterocyclischen Reihe wie Thienyl, Thenoyl, Furyl, Furoyl, Pyrryl, Pyrroyl, Pyridyl oder Pyridoyl. Nonionic substituents in the sense of the present invention are the non-dissociating substituents customary in dye chemistry, such as halogen, alkyl, aralkyl, alkenyl, aryl, hydroxy, alkoxy, aralkoxy, aryloxy, alkylthio, aralkylthio, arylthio, nitro, cyano, alkoxycarbonyl, Formyl, alkylcarbonyl, arylcarbonyl, aralkylcarbonyl, alk-oxycarbonyloxy, alkylcarbonylamino, arylcarbonylamino, alkylsulfonylamino, arylsulfonylamino, ureido, N-aryl- or N-alkyl-ureido, aryloxycarbonylamino, alkyloxycarbonyl-amino, carbamoyloyl, N-alkyl-carbonylamoyl Dialkylcarba-moyl, N-alkyl-N-aryl-carbamoyl, sulfamoyl, N-alkylsulfomoyl, NN-dialkyl-sulfamoyl, carboxylic acid alkyl ester, carboxylic acid aryl ester, sulfonic acid alkyl ester or sulfonic acid aryl ester groups, in the above Alkyl radicals are preferably 1-4 C atoms, and the aryl groups preferably belong to the phenyl or naphthalene series, and radicals such as thienyl, thenoyl, furyl, furoyl, pyrryl, pyrroyl, Pyridyl or pyridoyl.
Als anionische Reste An'"' kommen die für kationische Farbstoffe üblichen organischen und anorganischen Anionen in Betracht. The anionic residues An '' 'which are customary for cationic dyes are organic and inorganic anions.
Anorganische Anionen sind beispielsweise Fluorid, Chlorid, Bromid und Jodid, Perchlorat, Hydroxyl, Reste von S-hal-tigen Säuren, wie Hydrogensulfat, Sulfat, Disulfat und Amino-sulfat; Reste von Stickstoff-Sauerstoff-Säuren, wie Nitrat; Reste von Sauerstoffsäuren des Phosphors, wie Dihydrogen-phosphat, Hydrogenphosphat, Phosphat und Metaphosphat; Reste der Kohlensäure, wie Hydrogencarbonat und Carbonat; weitere Anionen von Sauerstoffsäuren und Komplexsäuren, wie Methosulfat, Äthosulfat, Hexafluorosilikat, Cyanat, Thio-eyanat, Hexacyanoferrat-(II), Hexacyanoferrat-(lll), Tri-und Tetrachlorozinkat, Tri- und Tetrabromozinkat, Stannat, Borat, Divanadat, Tetravanadat, Molybdat, Wolframat, Chromat, Bichromat und Tetrafluoroborat, sowie Anionen von Estern der Borsäure, wie des Glycerinesters der Borsäure und von Estern der Phosphorsäure, wie des Methylphosphats. Inorganic anions are, for example, fluoride, chloride, bromide and iodide, perchlorate, hydroxyl, residues of S-containing acids, such as hydrogen sulfate, sulfate, disulfate and amino sulfate; Residues of nitrogen-oxygen acids, such as nitrate; Residues of phosphoric oxygen acids, such as dihydrogen phosphate, hydrogen phosphate, phosphate and metaphosphate; Residues of carbonic acid such as hydrogen carbonate and carbonate; further anions of oxygen acids and complex acids, such as methosulfate, ethosulfate, hexafluorosilicate, cyanate, thio-eyanate, hexacyanoferrate (II), hexacyanoferrate (III), tri-and tetrachlorozincate, tri- and tetrabromozincate, stannate, borate, divanadan, divan Molybdate, tungstate, chromate, bichromate and tetrafluoroborate, as well as anions of esters of boric acid, such as the glycerol ester of boric acid, and of esters of phosphoric acid, such as methyl phosphate.
Organische Anionen sind beispielsweise Anionen gesättigter oder ungesättigter aliphatischer, cycloaliphatischer, aroma- Organic anions are, for example, anions of saturated or unsaturated aliphatic, cycloaliphatic, aromatic
15 tischer und heterocyclischer Carbonsäuren und Sulfonsäuren, wie Reste der Essigsäure, Chloressigsäure, Cyanessigsäure, Hydroxyessigsäure, Propionsäure, n-Buttersäure. i-Butter-säure, 2-Methyl-buttersäure, 2-Äthyl-buttersäure, Dichlor-essigsäure, Trichloressigsäure, Trifluoressigsäure, 2-Chlor-20 propionsäure, 3-Chlorpropionsäure, 2-Chlor-buttersäure, 15 table and heterocyclic carboxylic acids and sulfonic acids, such as residues of acetic acid, chloroacetic acid, cyanoacetic acid, hydroxyacetic acid, propionic acid, n-butyric acid. i-butter acid, 2-methyl-butyric acid, 2-ethyl-butyric acid, dichloroacetic acid, trichloroacetic acid, trifluoroacetic acid, 2-chloro-20-propionic acid, 3-chloropropionic acid, 2-chloro-butyric acid,
2-Hydroxypropionsäure. 3-Hydroxypropionsäure, O-Äthyl-glykolsäure. Thioglykolsäure, Glycerinsäure, Apfelsäure, Dodecyltetraäthylenglykolätherpropionsäure, 3-(Nonyloxy)-propionsäure, 3-(Isotridecyloxy)-propionsäure, 3-(Isotridecyl- 2-hydroxypropionic acid. 3-hydroxypropionic acid, O-ethyl glycolic acid. Thioglycolic acid, glyceric acid, malic acid, dodecyl tetraethylene glycol ether propionic acid, 3- (nonyloxy) propionic acid, 3- (isotridecyloxy) propionic acid, 3- (isotridecyl)
25 oxy)-diäthylenglykolätherpropionsäure, Ätherpropionsäure des Alkoholgemisches mit 6 bis 10 Kohlenstoffatomen, Thio-essigsäure, 6-Benzoylamino-2-chlorcapronsäure, Nonylphenol-tetraäthylenglykoläther-propionsäure, Nonylphenoldiäthylen-glykoläther-propionsäure, Dodecyltetraäthylenglykoläther-'0 propionsäure, Phenoxyessigsäure, Nonylphenoxyessigsäure, n-Valeriansäure, i-Valeriansäure, 2.2,2-Trimethylessigsäure, n-Capronsäure, 2-Äthyl-n-capronsäure, Stearinsäure, Ölsäure, Ricinolsäure, Palmitinsäure. n-Pelargonsäure, Laurinsäure. eines Gemisches aliphatischer Carbonsäuren mit 9 bis 11 35 Kohlenstoffatomen (Versatic-Säure 911 der SHELL), eines Gemisches aliphatischer Carbonsäuren mit 15 bis 19 Kohlenstoffatomen (Versatic-Säure 1519 der SHELL), des Kokosfettsäure-Vorlaufs, der Undecancarbonsäure, n-Tridecan-carbonsäure und eines Kokosfettsäuregemisches; der Acryl-40 säure. Methacrylsäure, Crotonsäure, Propargylsäure, Oxalsäure, Malonsäure, Bernsteinsäure, Glutarsäure, Adipinsäure, Pimelinsäure, Korksäure, Azelainsäure, des Isomerengemisches aus 2.2,4- und 2,4,4-Trimethyladipinsäure, Sebacinsäure, Iso-sebacinsäure (Isomerengemisch), Weinsäure, Zitronensäure, 45 Glyoxylsäure, Dimethyläther-a,a'-dicarbonsäure, Methylen-bis-thioglycolsäure, Dimethylsulfid-«,a'-dicarbonsäure, 2,2'-Dithio-di-n-propionsäure, Fumarsäure, Maleinsäure, Itacon-säure, Äthylen-bis-iminoessigsäure, Nitrilosulfonsäure, Me-thansulfonsäure, Äthansulfonsäure, Chlormethansulfonsäure, 50 2-Chloräthansulfonsäure und 2-Hydroxyäthansulfonsäure, Mersolat, d. h. C8-C,5 Paraffinsulfonsäure, erhalten durch C'hlorsulfierung von Paraffinöl. 25 oxy) -diethylene glycol ether-propionic acid, ether propionic acid of the alcohol mixture with 6 to 10 carbon atoms, thio-acetic acid, 6-benzoylamino-2-chlorocaproic acid, nonylphenol-tetraethylene glycol ether-propionic acid, nonylphenol diethylene glycol, propyl ether, dodiacetyl ether, dodiacetyl ether, dodiacetate, phenyl ethylenedioxyphenyl, propionic acid, dodiacetate, dodiacetyl ether, phenyl ethylenedioxyne, -Valerianic acid, i-valeric acid, 2,2,2-trimethylacetic acid, n-caproic acid, 2-ethyl-n-caproic acid, stearic acid, oleic acid, ricinoleic acid, palmitic acid. n-pelargonic acid, lauric acid. a mixture of aliphatic carboxylic acids with 9 to 11 35 carbon atoms (Versatic acid 911 from SHELL), a mixture of aliphatic carboxylic acids with 15 to 19 carbon atoms (Versatic acid 1519 from SHELL), the coconut fatty acid precursor, the undecane carboxylic acid, n-tridecane carboxylic acid and a coconut fatty acid mixture; the acrylic 40 acid. Methacrylic acid, crotonic acid, propargyl acid, oxalic acid, malonic acid, succinic acid, glutaric acid, adipic acid, pimelic acid, suberic acid, azelaic acid, the isomer mixture of 2,2,4- and 2,4,4-trimethyladipic acid, sebacic acid, isosebacic acid (isomer mixture), tartaric acid, citric acid , 45 glyoxylic acid, dimethyl ether-a, a'-dicarboxylic acid, methylene-bis-thioglycolic acid, dimethyl sulfide - «, a'-dicarboxylic acid, 2,2'-dithio-di-n-propionic acid, fumaric acid, maleic acid, itaconic acid, ethylene -bis-iminoacetic acid, nitrilosulfonic acid, methanesulfonic acid, ethanesulfonic acid, chloromethanesulfonic acid, 50 2-chloroethanesulfonic acid and 2-hydroxyethanesulfonic acid, mersolate, d. H. C8-C, 5 paraffin sulfonic acid, obtained by chlorine sulfation of paraffin oil.
Geeignete Anionen cycloaliphatischer Carbonsäuren sind z. B. die Anionen der Cyclohexancarbonsäure, Cyclohexen-3-55 carbonsäure und Anionen araliphatischer Monocarbonsäuren sind z. B. Afiionen der Phenylessigsäure, 4-Methylphenyl-essigsäure und Mandelsäure. Suitable anions of cycloaliphatic carboxylic acids are e.g. B. the anions of cyclohexane carboxylic acid, cyclohexene-3-55 carboxylic acid and anions of araliphatic monocarboxylic acids are, for. B. Afions of phenylacetic acid, 4-methylphenylacetic acid and mandelic acid.
Geeignete Anionen aromatischer Carbonsäuren sind beispielsweise die Anionen der Benzoesäure, 2-Methylbenzoe-60 säure, 3-Methylbenzoesäure, 4-Methylbenzoesäure, 4-tert.-Butylbenzocsäure, 2-Brombenzoesäure, 2-Chlorbcnzoesäure, Suitable anions of aromatic carboxylic acids are, for example, the anions of benzoic acid, 2-methylbenzoic acid, 3-methylbenzoic acid, 4-methylbenzoic acid, 4-tert-butylbenzoic acid, 2-bromobenzoic acid, 2-chlorobenzoic acid,
3-C"hlorbenzoesäure, 4-Chlorbenzoesäure, 2,4-Dichlorbenzoe-säure, 2,5-Dichlorbenzoesäure, 2-Nitrobenzoesäure, 3-Nitro-benzoesäure, 4-Nitrobenzoesäure, 2-Chlor-4-nitrobenzoe- 3-C "chlorobenzoic acid, 4-chlorobenzoic acid, 2,4-dichlorobenzoic acid, 2,5-dichlorobenzoic acid, 2-nitrobenzoic acid, 3-nitro-benzoic acid, 4-nitrobenzoic acid, 2-chloro-4-nitrobenzoic acid
55 säure, 6-Chlor-3-nitro-benzoesäure, 2,4-Dinitrobenzoesäure, 3,4-Dinitrobenzoesäure, 3,5-Dinitrobenzoesäure, 2-Hydroxy-benzoesäure, 3-Hydroxybenzoesäure, 4-Hydroxybenzoesäure, 2-Mercaptobenzoesäure, 4-Nitro-3-methylbenzoesäure, 55 acid, 6-chloro-3-nitro-benzoic acid, 2,4-dinitrobenzoic acid, 3,4-dinitrobenzoic acid, 3,5-dinitrobenzoic acid, 2-hydroxy-benzoic acid, 3-hydroxybenzoic acid, 4-hydroxybenzoic acid, 2-mercaptobenzoic acid, 4 -Nitro-3-methylbenzoic acid,
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5-Nitro-2-hydroxybenzoesäure, 3-Nitro-3-hydroxybenzoe-säure, 4-Methoxybenzoesäure, 3-Nitro-4-methoxybenzoe-säure, 4-Chlor-3-hydroxybenzoesäure, 3-Chlor-4-hydroxy-benzoesäure, 5-Chlor-2-hydroxy-3-methylbenzoesäure, 4-Äthylmercapto-2-chlorbenzoesäure, 2-Hydroxy-3-methyl-benzoesäure, 6-Hydroxy-3-methylbenzoesäure, 2-Hydroxy-4-methylbenzoesäure, 6-Hydroxy-2,4-dimethylbenzoesäure, 5-nitro-2-hydroxybenzoic acid, 3-nitro-3-hydroxybenzoic acid, 4-methoxybenzoic acid, 3-nitro-4-methoxybenzoic acid, 4-chloro-3-hydroxybenzoic acid, 3-chloro-4-hydroxybenzoic acid, 5-chloro-2-hydroxy-3-methylbenzoic acid, 4-ethylmercapto-2-chlorobenzoic acid, 2-hydroxy-3-methylbenzoic acid, 6-hydroxy-3-methylbenzoic acid, 2-hydroxy-4-methylbenzoic acid, 6-hydroxy- 2,4-dimethylbenzoic acid,
6-Hydroxy-3-tert.-butylbenzoesäure, Phthalsäure, Tetrachlor-phthalsäure, 4-Hydroxyphthalsäure, 4-Methoxyphthalsäure, Isophthalsäure, 4-Chlorisophthalsäure, 5-Nitro-isophthalsäure, Terephthalsäure, Nitroterephthalsäure und Diphenylcarbon-säure-(3,4), o-Vanillinsäure, 3-Sulfobenzoesäure, Benzol-tetracarbonsäure-( 1,2,4,5), Naphthalintetracarbonsäure-(1,4,5,8), Biphenylcarbonsäure-(4), Abietinsäure, Phthal-säure-mono-n-butylester, Terephthalsäuremonomethylester, 3-Hydroxy-5,6,7,8-tetrahydronaphthalincarbonsäure-(2), 2-Hydroxynaphthoesäure-(l) und Anthrachinoncarbon-säure-(2). 6-hydroxy-3-tert-butylbenzoic acid, phthalic acid, tetrachlorophthalic acid, 4-hydroxyphthalic acid, 4-methoxyphthalic acid, isophthalic acid, 4-chloroisophthalic acid, 5-nitro-isophthalic acid, terephthalic acid, nitroterephthalic acid and diphenyl carbonate , o-vanillic acid, 3-sulfobenzoic acid, benzene-tetracarboxylic acid (1,2,4,5), naphthalene tetracarboxylic acid (1,4,5,8), biphenylcarboxylic acid (4), abietic acid, phthalic acid mono-n -butyl ester, terephthalic acid monomethyl ester, 3-hydroxy-5,6,7,8-tetrahydronaphthalenecarboxylic acid- (2), 2-hydroxynaphthoic acid- (1) and anthraquinone carbonate- (2).
Als Anionen heterocyelischer Carbonsäuren geeignet sind beispielsweise die Anionen der Brenzschleimsäure, Dehydro-schleimsäure, Indolyl-(3)-essigsäure. Suitable anions of heterocyclic carboxylic acids are, for example, the anions of pyruvic acid, dehydro-mucic acid, indolyl- (3) -acetic acid.
Geeignete Anionen aromatischer Sulfonsäuren sind z. B. die Anionen der Benzolsulfonsäure, Benzoldisulfonsäure- Suitable anions of aromatic sulfonic acids are e.g. B. the anions of benzenesulfonic acid, benzenedisulfonic acid
(1.3), 4-Chlorbenzolsulfonsäure, 3-Nitrobenzolsulfonsäure, 6-Chlor-3-nitrobenzolsulfonsäure, Toluolsulfonsäure-(4), Toluolsulfonsäure-(2), Toluol-w-sulfonsäure, 2-Chlortoluol-sulfonsäure-(4), 1-Hydroxybenzolsulfonsäure, n-Dodecyl-benzolsulfonsäure. 1,2,3,4-Tetrahydronaphthalinsulfonsäure-(6), Naphthalinsulfonsäure-(l), Naphthalindisulfonsäure- (1.3), 4-chlorobenzenesulfonic acid, 3-nitrobenzenesulfonic acid, 6-chloro-3-nitrobenzenesulfonic acid, toluenesulfonic acid (4), toluenesulfonic acid (2), toluene-w-sulfonic acid, 2-chlorotoluene sulfonic acid (4), 1- Hydroxybenzenesulfonic acid, n-dodecyl-benzenesulfonic acid. 1,2,3,4-tetrahydronaphthalenesulfonic acid- (6), naphthalenesulfonic acid- (1), naphthalenedisulfonic acid-
(1.4) oder -(1,5), Naphthalintrisulfonsäure-(l,3,5), Naphthol-( 1 )-sulfonsäure-(2), 5-Nitronaphthalinsulfonsäure-(2), Stilbendisulfonsäure-(2,2') und Biphenylsulfonsäure-(2). (1.4) or - (1,5), naphthalenetrisulfonic acid (1,3,5), naphthol (1) sulfonic acid (2), 5-nitronaphthalenesulfonic acid (2), stilbenedisulfonic acid (2,2 ') and Biphenylsulfonic acid- (2).
Ein geeignetes Anion heterocyclischer Sulfonsäuren ist z. B. das Anion der Chinolinsulfonsäure-(5). A suitable anion of heterocyclic sulfonic acids is e.g. B. the anion of quinoline sulfonic acid (5).
Weiterhin kommen die Anionen von Arylsulfin-, -phos-phon- und -phosphonigsäuren, wie Benzolsulfin- und Benzol-phosphonsäure in Betracht. Furthermore, the anions of arylsulfinic, -phosphonic and -phosphonous acids, such as benzenesulfinic and benzene-phosphonic acid, are suitable.
Bevorzugt sind farblose oder nahezu farblose Anionen. Für das Färben aus wässriger Lösung sind solche Anionen bevorzugt, die die Wasserlöslichkeit des Farbstoffs nicht zu stark beeinträchtigen. Für das Färben aus wässriger Dispersion ist 5 dieser Gesichtspunkt bei der Wahl der Anionen ohne Belang. Für das Färben aus organischen Lösungsmitteln sind vielfach auch solche Anionen bevorzugt, die die Löslichkeit des Farbstoffs in organischen Lösungsmitteln fördern oder zumindest nicht negativ beeinflussen; insbesondere sind hier die Anionen 10 organischer Mono- und Dicarbonsäuren mit etwa 4 bis 30 Kohlenstoffatomen zu nennen. Colorless or almost colorless anions are preferred. Anions which do not impair the water solubility of the dye too much are preferred for dyeing from aqueous solution. This aspect is irrelevant for the choice of anions for dyeing from aqueous dispersion. Anions which promote the solubility of the dye in organic solvents or at least do not negatively influence it are often preferred for dyeing from organic solvents; In particular, the anions of 10 organic mono- and dicarboxylic acids with about 4 to 30 carbon atoms should be mentioned here.
Die Farbstoffe der allgemeinen Formel (I) werden erhalten, indem man Aminopyrazole der allgemeinen Formel The dyes of the general formula (I) are obtained by using aminopyrazoles of the general formula
15 15
20 20th
25 25th
R1 *2 n i R1 * 2 n i
r worin R, R, und R2 die in Formel I angegebene Bedeutung haben, nach an sich bekannten Methoden diazotiert, die so erhaltenen Diazoniumverbindungen mit Kupplungskomponenten der Formel r wherein R, R, and R2 have the meaning given in formula I, diazotized according to methods known per se, the diazonium compounds thus obtained with coupling components of the formula
30 30th
.rr .rr
(f>n (f> n
<CV„ <CV "
vi vi
35 35
worin R4, Rs, R6, m und n die in Formel I angegebene Bedeutung haben, zu Monoazofarbstoffen der Formel wherein R4, Rs, R6, m and n have the meaning given in formula I, to monoazo dyes of the formula
R* R2 R * R2
R6 R6
/"V n=n y • / "V n = n y •
1 fr > (ch?) 1 fr> (ch?)
r ^ 4 ra ^ r ^ 4 ra ^
vereinigt und die erhaltenen Monoazofarbstoffe mit alkylierend wirkenden Verbindungen der Formel n combined and the monoazo dyes obtained with alkylating compounds of formula n
-(Rr ) - (Rr)
5 m 5 m
VII VII
Rj-X Rj-X
Vili Vili
50 50
worin R3 die in Formel I genannte Bedeutung hat, und X für eine als Anion An1"' abspaltbare Gruppe steht, umsetzt. in which R3 has the meaning given in formula I, and X represents a group which can be split off as the anion An1 "'.
Die Diazokomponenten der Formel (V) können nach literaturbekannten Methoden aus/3-Ketonitrilen und mono-substituierten Hydrazinen hergestellt werden. The diazo components of the formula (V) can be prepared from / 3-ketonitriles and mono-substituted hydrazines by methods known from the literature.
Beispielhaft seien folgende Diazokomponenten aufgezählt: The following diazo components are listed as examples:
3,4-Dimethyl-5-amino-pyrazol, 3,4-Diäthyl-5-amino-pyrazol, 3,4-Diisopropyl-5-amino-pyrazol, 3-Methyl-4-äthyl-5-amino-pyrazol, 3-Äthyl-4-methyl-5-amino-pyrazol, 3-Me-thyl-4-isopropyl-5-amino-pyrazol, 3-Phenyl-4-methyl-5-amino-pyrazol, 3,4-Diphenyl-5-amino-pyrazol, 1,3,4-Tri-methyl-5-amino-pyrazol, 1,3,4-Triäthyl-5-amino-pyrazol, 1,3,4-Triisopropyl-5-amino-pyrazol, 1,3,4-Triphenyl-5-amino-pyrazol, l-Methyl-3,4-diäthyl-5-amino-pyrazol, 1-Methyl-3,4-diisopropyl-5-amino-pyrazol, l-Methyl-3,4-diphenyl-5-amino-pyrazol, 1 -Äthyl-3,4-dimethyl-5-amino-pyrazol, l-Äthyl-3,4-diisopropyl-5-amino-pyrazol, l-ÄthyI-3,4-di-phenyl-5-amino-pyrazol, 1 -Isopropyl-3,4-dimethyl-5-amino- 3,4-dimethyl-5-aminoprazole, 3,4-diethyl-5-aminopyrazole, 3,4-diisopropyl-5-aminopyrazole, 3-methyl-4-ethyl-5-aminopyrazole, 3-ethyl-4-methyl-5-amino-pyrazole, 3-methyl-4-isopropyl-5-amino-pyrazole, 3-phenyl-4-methyl-5-amino-pyrazole, 3,4-diphenyl- 5-amino-pyrazole, 1,3,4-tri-methyl-5-amino-pyrazole, 1,3,4-triethyl-5-amino-pyrazole, 1,3,4-triisopropyl-5-amino-pyrazole, 1,3,4-triphenyl-5-aminoprazole, l-methyl-3,4-diethyl-5-aminopyrazole, 1-methyl-3,4-diisopropyl-5-aminopyrazole, l-methyl 3,4-diphenyl-5-aminopyrazole, 1-ethyl-3,4-dimethyl-5-aminopyrazole, l-ethyl-3,4-diisopropyl-5-aminopyrazole, l-ethylI-3, 4-di-phenyl-5-amino-pyrazole, 1-isopropyl-3,4-dimethyl-5-amino-
65 65
pyrazol, l-Isopropyl-3,4-diäthyl-5-amino-pyrazol, 1-Isopropyl-3,4-diphenyl-5-amino-pyrazol, l-Phenyl-3,4-dimethyl-5-amino-pyrazol, l-Phenyl-3,4-diäthyl-5-amino-pyrazol, 1-Phe-nyl-3,4-diisopropyl-5-amino-pyrazol, 1 -Phenyl-3-methyl-4-äthyl-5-amino-pyrazol, 1 -Phenyl-3-äthyl-4-methyl-5-amino-pyrazol, l,3-Dimethyl-4-äthyl-5-amino-pyrazol, 1,3-Diäthyl- pyrazole, l-isopropyl-3,4-diethyl-5-amino-pyrazole, 1-isopropyl-3,4-diphenyl-5-amino-pyrazole, l-phenyl-3,4-dimethyl-5-amino-pyrazole, l-phenyl-3,4-diethyl-5-amino-pyrazole, 1-phenyl-3,4-diisopropyl-5-amino-pyrazole, 1-phenyl-3-methyl-4-ethyl-5-amino- pyrazole, 1-phenyl-3-ethyl-4-methyl-5-amino-pyrazole, l, 3-dimethyl-4-ethyl-5-amino-pyrazole, 1,3-diethyl
4-methyl-5-amino-pyrazol, 1,3-Diisopropyl-4-methyl-5-amino-pyrazol, l,3-Diphenyl-4-methyl-5-amino-pyrazol, 1,4-Dimethyl-3-äthyl-5-amino-pyrazol, 1,4-Diäthyl-3-methyl-5-amino-pyrazol, 1,4-Diisopropyl-3-methyl-5-amino-pyrazol, 4-methyl-5-aminopyrazole, 1,3-diisopropyl-4-methyl-5-aminopyrazole, 1,3-diphenyl-4-methyl-5-aminopyrazole, 1,4-dimethyl-3- ethyl 5-amino-pyrazole, 1,4-diethyl-3-methyl-5-amino-pyrazole, 1,4-diisopropyl-3-methyl-5-amino-pyrazole,
1,4-Diphenyl-3-methyl-5-amino-pyrazol, 1,3-Diphenyl-4-äthyl-5-amino-pyrazol, 1,4-Diphenyl-3-äthyl-5-amino-pyrazol, 1 -Methyl-3,4-dibutyl-5-amino-pyrazol, 1 -Isopropyl-3,4-di-butyl-5-amino-pyrazol, 1 -Phenyl-3,4-dibutyl-5-amino-pyrazol, 1 -Phenyl-3-butyl-4-methyl-5-amino-pyrazol, 3,4-Trimethylen- 1,4-diphenyl-3-methyl-5-aminopyrazole, 1,3-diphenyl-4-ethyl-5-aminopyrazole, 1,4-diphenyl-3-ethyl-5-aminopyrazole, 1 - Methyl-3,4-dibutyl-5-amino-pyrazole, 1-isopropyl-3,4-di-butyl-5-amino-pyrazole, 1-phenyl-3,4-dibutyl-5-amino-pyrazole, 1 - Phenyl-3-butyl-4-methyl-5-aminopyrazole, 3,4-trimethylene
5-amino-pyrazol, 1 -Methyl-3,4-trimethylen-5-amino-pyrazol, l-Äthyl-3,4-trimethylen-5-amino-pyrazol, l-Isopropyl-3,4-trimethylen-5-amino-pyrazol, l-Phenyl-3,4-trimethylen-5-amino-pyrazol, 3,4-Tetramethylen-5-amino-pyrazoI, 1-Methyl-3,4-tetramethylen-5-amino-pyrazol, l-Äthyl-3,4-tetramethy-len-5-amino-pyrazol, l-Isopropyl-3,4-tetramethylen-5-amino-pyrazol, l-Phenyl-3,4-tetramethylen-5-amino-pyrazol, l-(2'-Chlorphenyl)-3,4-dimethyl-5-amino-pyrazol, l-(4'-Chlor- 5-amino-pyrazole, 1-methyl-3,4-trimethylene-5-amino-pyrazole, l-ethyl-3,4-trimethylene-5-amino-pyrazole, l-isopropyl-3,4-trimethylene-5- amino-pyrazole, l-phenyl-3,4-trimethylene-5-amino-pyrazole, 3,4-tetramethylene-5-amino-pyrazoI, 1-methyl-3,4-tetramethylene-5-amino-pyrazole, l- Ethyl-3,4-tetramethylene-5-amino-pyrazole, l-isopropyl-3,4-tetramethylene-5-amino-pyrazole, l-phenyl-3,4-tetramethylene-5-amino-pyrazole, l- (2'-chlorophenyl) -3,4-dimethyl-5-aminopyrazole, 1- (4'-chloro-
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phenyl)-3,4-dimethyl-5-amino-pyrazol, l-(2'-Methylphenyl)-3,4-dimethyl-5-amino-pyrazol, 1 -(4'-Methylphenyl)-3,4-di-methyl-5-amino-pyrazol, l-Sulfolanyl-(3')-dimethyl-5-amino-pyrazol, l-Cyclohexyl-3,4-dimethyl-5-amino-pyrazol, 1 -Benzyl-3,4-dimethyl-5-amino-pyrazol, 1 -Benzthiazolyl-(2')-3,4-dimethyl-5-amino-pyrazol, l-Pyridyl-(2')-3,4-di-methyl-5-amino-pyrazol, l-Pyrimidyl-(2')-3,4-dimethyl-5-amino-pyrazol, l-(2'-Chlorphenyl)-3,4-trimethylen-5-amino-pyrazol, l-(4'-Chlorphenyl)-3,4-trimethylen-5-amino-pyrazol, l-(2'-Methylphenyl)-3,4-trimethyIen-5-amino-pyrazol, l-(4'-Methylphenyl)-3,4-trimethylen-5-amino-pyrazol, 1 -Sulfolanyl-(3' )-3,4-trirnethylen-5-amino-pyrazol, 1 -Cyclo-hexyl-3,4-trimethylen-5-amino-pyrazol, l-Benzyl-3,4-tri-methylen-5-amino-pyrazol, l-Benzthiazolyl-(2')-3,4-tri-methylen-5-amino-pyrazol, l-Pyridyl-(2')-3,4-trimethylen-5-amino-pyrazol, l-Pyrimidyl-(2')-3,4-trimethylen-5-amino-pyrazol, l-(2'-Chlorphenyl)-3,4-tetramethylen-5-amino-pyrazol, l-(4'-Chlorphenyl)-3,4-tetramethylen-5-amino-pyrazol, l-(2'-Methylphenyl)-3,4-tetramethylen-5-amino-pyrazol, l-(4'-Methylphenyl)-3,4-tetramethylen-5-amino-pyrazol, l-Sulfolanyl-(3')-3,4-tetramethylen-5-amino-pyra-zol, l-Cyclohexyl-3,4-tetramethylen-5-amino-pyrazol, 1-Ben-zyl-3,4-tetramethylen-5-amino-pyrazol, 1-Benzthiazolyl-(2')-3,4-tetramethylen-5-amino-pyrazol, 1 -Pyridyl-(2')-3,4-tetramethylen-5-amino-pyrazol, 1 -Pyrimidyl-(2' )-3,4-tetramethylen-5-amino-pyrazol, 1 -(3' -Chlorphenyl)-3,4-dimethyl-5-amino-pyrazol, 1 -(4'-Nitro-phenyl)-3,4-dimethyI-5-amino-pyrazol, l-(/S-Cyanäthyl)-3,4-dimethyl-5-amino-pyrazol, l-(|ö-Cyanäthyl)-3-äthyl-4-methyl-5-amino-pyrazol, l-(/3-Hydroxyäthyl)-3,4-dimethyl-5-amino-pyrazol, l-(/3-Hydroxyäthyl)-3-äthyl-4-methyl-5-amino-pyrazol, l-(ß-Hy-droxyäthyl)-3-methyl-4-phenyl-5-amino-pyrazol, 1 -(/3-Cyan-äthyl)-3,4-trimethylen-5-amino-pyrazol, l-(/3-Cyanäthyl)-3,4-tetramethylen-5-amino-pyrazol, 1 -(/3-Hydroxyäthyl)-3,4-trimethyIen-5-amino-pyrazol, l-(/3-Hydroxyäthyl)-3,4-tetramethylen-5-amino-pyrazol. phenyl) -3,4-dimethyl-5-aminopyrazole, l- (2'-methylphenyl) -3,4-dimethyl-5-aminopyrazole, 1 - (4'-methylphenyl) -3,4-di -methyl-5-amino-pyrazole, l-sulfolanyl- (3 ') - dimethyl-5-amino-pyrazole, l-cyclohexyl-3,4-dimethyl-5-amino-pyrazole, 1-benzyl-3,4- dimethyl-5-amino-pyrazole, 1-benzthiazolyl- (2 ') - 3,4-dimethyl-5-amino-pyrazole, l-pyridyl- (2') - 3,4-dimethyl-5-amino- pyrazole, l-pyrimidyl- (2 ') - 3,4-dimethyl-5-amino-pyrazole, l- (2'-chlorophenyl) -3,4-trimethylene-5-amino-pyrazole, l- (4'- Chlorophenyl) -3,4-trimethylene-5-amino-pyrazole, l- (2'-methylphenyl) -3,4-trimethylene-5-amino-pyrazole, l- (4'-methylphenyl) -3,4-trimethylene -5-amino-pyrazole, 1-sulfolanyl- (3 ') -3,4-trirethylene-5-amino-pyrazole, 1-cyclo-hexyl-3,4-trimethylene-5-amino-pyrazole, l-benzyl- 3,4-tri-methylene-5-amino-pyrazole, l-benzothiazolyl- (2 ') - 3,4-tri-methylene-5-amino-pyrazole, l-pyridyl- (2') - 3,4- trimethylene-5-amino-pyrazole, l-pyrimidyl- (2 ') - 3,4-trimethylene-5-amino-pyrazole, l- (2'-chlorophenyl) -3,4-tetramethylene-5-amino-pyrazole, l- (4'-chlorophenyl) -3,4-tet ramethylene-5-amino-pyrazole, l- (2'-methylphenyl) -3,4-tetramethylene-5-amino-pyrazole, l- (4'-methylphenyl) -3,4-tetramethylene-5-amino-pyrazole, l-Sulfolanyl- (3 ') - 3,4-tetramethylene-5-amino-pyrazole, l-cyclohexyl-3,4-tetramethylene-5-amino-pyrazole, 1-benzyl-3,4-tetramethylene -5-aminopyrazole, 1-benzothiazolyl- (2 ') - 3,4-tetramethylene-5-aminopyrazole, 1-pyridyl- (2') - 3,4-tetramethylene-5-aminopyrazole, 1 -Pyrimidyl- (2 ') -3,4-tetramethylene-5-amino-pyrazole, 1 - (3' -chlorophenyl) -3,4-dimethyl-5-amino-pyrazole, 1 - (4'-nitro-phenyl ) -3,4-dimethyl-5-amino-pyrazole, l - (/ S-cyanoethyl) -3,4-dimethyl-5-amino-pyrazole, l- (| ö-cyanoethyl) -3-ethyl-4- methyl-5-amino-pyrazole, l - (/ 3-hydroxyethyl) -3,4-dimethyl-5-amino-pyrazole, l - (/ 3-hydroxyethyl) -3-ethyl-4-methyl-5-amino- pyrazole, l- (ß-hydroxyethyl) -3-methyl-4-phenyl-5-amino-pyrazole, 1 - (/ 3-cyanoethyl) -3,4-trimethylene-5-amino-pyrazole, l - (/ 3-cyanoethyl) -3,4-tetramethylene-5-amino-pyrazole, 1 - (/ 3-hydroxyethyl) -3,4-trimethylene-5-amino-pyrazole, l - (/ 3-hydroxyethyl) - 3,4-tetramethylene -5-amino-pyrazole.
Geeignete Kupplungskomponenten der Formel (VI) sind beispielsweise: Suitable coupling components of the formula (VI) are, for example:
N-Benzyl-anilin, 3-(N-Benzyl-amino)-toluol, 3-(N-Ben-zyl-amino)-chlorbenzol, 3-(N-Benzyl-amino)-anisol, 2-(N-Benzyl-amino)-4-methyl-anisol, 3-(N-Benzyl-amino)-acet-anilid, N-(4'-Chlor-benzyl)-anilin, N-(3'-Nitro-benzyl)-anilin, N-(4'-Methyl-benzyl)-anilin, N-(4'-Methoxy-benzyl)-anilin, N-(/3-Phenyläthyl)-anilin, 3-[N-(/?-Phenyläthyl)-amino]-toluol, 2-[N-(/?-Phenyläthyl)-amino]-4-methyl-anisol, 3-[N-(/S-Phenyläthyl)-amino]-chlorbenzol, 3-[N-(/3-Phenyl-äthyl)-amino]-anisol, 3-[N-(/3-Phenyläthyl)-amino]-actani-\id, N-J/3-(4'-Ch\orphenyl)-äthyl]-anilin, N-Methyl-N-ben-zyl-anilin, N-Äthyl-N-benzyl-anilin, N-Propyl-N-benzyl-anilin, N-Butyl-N-benzyl-anilin, N,N-Dibenzyl-anilin, N-Cyelohexyl-N-benzyl-anilin, 3-(N-Methyl-N-benzyl-amino)-toluol, 3-(N-Äthyl-N-benzyl-amino)-toluol, 3-(N-Propyl-N-benzyl-amino)-toluol, 3-(N-Butyl-N-benzyl-amino)-toluol, 3-(N,N-Dibenzyl-amino)-toluol, 3-(N-Cyclohexyl-N-benzyl-amino)-toluol, 3-(N-Äthyl-N-benzyl-amino)-chlorbenzol, 3-(N-Äthyl-N-benzyl-amino)-anisol, 3-(N-Cyclohexyl-N-benzyl-amino)-anisol, 3-(N,N-Dibenzyl-amino)-anisoI, 2-(N-Äthyl-N-benzyl-amino)-4-methyl-anisol, 2-(N,N-Dibenzyl-amino)-4-methyl-anisol, 3-(N-Äthyl-N-benzyl-amino)-4-methyl-anisol, 2-(N,N-Dibenzyl-amino)-4-methyl-anisol, 3-(N-Äthyl-N-benzyl-amino)-acetanilid, 3-(N-Butyl-N-benzyl-amino)-acetanilid, 3-(N,N-Dibenzyl-amino)-acetanilid, N-Äthyl-N-(4'-chlor-benzyl)-anilin, N-Cyclohexyl-N-(4'-ehlorbenzyl)-anilin, N,N-Bis-(4'-chlor-benzyI)-anilin, N-Methyl-N-(/?-phenyl-äthyl)-anilin, N-Äthyl-N-(/J-phenyläthyl)-anilin, N-Butyl-N-(/3-phenyläthyl)-anilin, N-Benzyl-N-(/?-phenyläthyl)-anilin, N-Cyclohexyl-N-(/3-phenyläthyl)-anilin, 3-[N-Methyl-N-(/3-phenyläthyl)-amino]-toluol, 3-[N-Äthyl-N-(ß-phenyl- N-benzylaniline, 3- (N-benzylamino) toluene, 3- (N-benzylamino) chlorobenzene, 3- (N-benzylamino) anisole, 2- (N-benzyl -amino) -4-methyl-anisole, 3- (N-benzyl-amino) -acetanilide, N- (4'-chlorobenzyl) aniline, N- (3'-nitro-benzyl) aniline, N- (4'-methylbenzyl) aniline, N- (4'-methoxybenzyl) aniline, N - (/ 3-phenylethyl) aniline, 3- [N - (/? - phenylethyl) amino ] toluene, 2- [N - (/? - phenylethyl) amino] -4-methyl-anisole, 3- [N - (/ S-phenylethyl) amino] chlorobenzene, 3- [N - (/ 3 -Phenyl-ethyl) -amino] -anisole, 3- [N - (/ 3-phenylethyl) -amino] -actani- \ id, NJ / 3- (4'-chlorophenyl) -ethyl] -aniline, N -Methyl-N-benzyl-aniline, N-ethyl-N-benzyl-aniline, N-propyl-N-benzyl-aniline, N-butyl-N-benzyl-aniline, N, N-dibenzyl-aniline, N -Yelohexyl-N-benzyl-aniline, 3- (N-methyl-N-benzyl-amino) -toluene, 3- (N-ethyl-N-benzyl-amino) -toluene, 3- (N-propyl-N- benzylamino) toluene, 3- (N-butyl-N-benzylamino) toluene, 3- (N, N-dibenzylamino) toluene, 3- (N-cyclohexyl-N-benzylamino) toluene, 3- (N-ethyl-N-benzylamino) chlorobenzene, 3- (N-ethyl-N-benzylamino) anisole, 3- (N-cyclohexyl-N-benzylamino) anisole, 3- (N, N-dibenzylamino) anisole, 2- (N-ethyl-N-benzylamino) -4-methylanisole, 2- (N, N-dibenzyl-amino) -4-methyl-anisole, 3- (N-ethyl-N-benzyl-amino) -4-methyl-anisole, 2- (N, N-dibenzyl-amino) -4- methyl anisole, 3- (N-ethyl-N-benzyl-amino) -acetanilide, 3- (N-butyl-N-benzyl-amino) -acetanilide, 3- (N, N-dibenzyl-amino) -acetanilide, N-ethyl-N- (4'-chlorobenzyl) aniline, N-cyclohexyl-N- (4'-chlorobenzyl) aniline, N, N-bis- (4'-chlorobenzyl) aniline, N -Methyl-N - (/? - phenylethyl) aniline, N-ethyl-N - (/ J-phenylethyl) aniline, N-butyl-N - (/ 3-phenylethyl) aniline, N-benzyl- N - (/? - phenylethyl) aniline, N-cyclohexyl-N - (/ 3-phenylethyl) aniline, 3- [N-methyl-N - (/ 3-phenylethyl) amino] toluene, 3- [ N-ethyl-N- (ß-phenyl-
äthyl)-amino]-toluol, 3-[N-Benzyl-N-(/?-phenyläthyl)-amino]-toluol, 3-[N-Cyclohexyl-N-(/3-phenyläthyI)-amino]-toluol, 2-[N-Äthyl-N-(/3-phenyläthyl)-amino]-4-methyl-benzol, 2-[N-Benzyl-N-(/3-phenyläthyl)-amino]-4-methyl-benzol, ethyl) amino] toluene, 3- [N-benzyl-N - (/? - phenylethyl) amino] toluene, 3- [N-cyclohexyl-N - (/ 3-phenylethyI) amino] toluene, 2- [N-ethyl-N - (/ 3-phenylethyl) amino] -4-methyl-benzene, 2- [N-benzyl-N - (/ 3-phenylethyl) amino] -4-methyl-benzene,
2-[N-Cyclohexyl-N-(/3-phenyläthyl)-amino]-4-methyl-benzol, 2- [N-cyclohexyl-N - (/ 3-phenylethyl) amino] -4-methyl-benzene,
3-[N-Äthyl-N-(/3-phenyläthyl)-amino]-anisol, 3-[N-Benzyl-N-(/3-phenyläthyl)-amino]-anisoI, 3-[-Cyclohexyl-N-(/3-phe-nyläthyl)-amino]-anisol, 3-[N-Äthyl-N-(/3-phenyIäthyI)-aminoj-acetanilid, 3-[N-Benzyl-N-(/?-phenyläthyl)-amino]-acetanilid, 3-[N-Cyclohexyl-N-(/3-phenyläthyl)-amino]-acetanilid, N,N-Bis-/3-phenyläthyl-anilin, 3-[N,N-Bis-(/?-phe-nyläthyl)-amino]-toluol, N-(/3-Hydroxyäthyl)-N-benzyl-anilin, N-(/S-Cyanäthyl)-N-benzyl-anilin, N-(j3-Acetoxy-äthyl)-N-benzyl-anilin, N-(/3-Propionyloxy)-N-benzyl-anilin, N-(/?-Methoxycarbonyläthyl)-N-benzyl-anilin, N-(/3-Äthoxy-carbonyläthyl)-N-benzyl-anilin, N-(/3-Methoxycarbonyloxy-äthyl)-N-benzyl-anilin, N-(/3-Äthoxyearbonyloxyäthyl)-N-benzyl-anilin, N-^-Methoxyäthy^-N-benzyl-anilin, N-(ß-Äthoxyäthyl)-benzylanilin, N-(/3-Phenoxyäthyl)-N-benzyl-anilin, N-(/3-Phenoxyacetoxyäthyl)-N-benzyl-anilin, N-(ß-Aeetylamino-äthyl)-N-benzyl-anilin, N-(y-Acetylaminopro-pyl)-N-benzyl-anilin, N-(/?-Chloräthyl)-N-benzyl-anilin, N-(/3-Dimethylaminoäthyl)-N-benzyl-anilin, N-(/3-Diäthyl-aminoäthyl)-N-benzyl-anilin, N-(y-Dimethylaminopropyl)-N-benzyl-anilin, 3-[N-Benzyl-N-(/3-hydroxy-äthyI)-amino]-toluol, 3-[N-Benzyl-N-(/S-eyanäthyl)-amino]-toluol, 3-[N-BenzyI-N-(/3-aeetoxyäthyl)-amino]-toIuol, 3-[N-Benzyl-N-(/?-propionyloxy)-amino]-toluol, 3-(N-Benzyl-N-(/3-meth-oxycarbonyläthyl)-amino]-toluol, 3-[N-Benzyl-N-(/3-äthoxy-carbonyläthyl)-amino]-toluol, 3-[N-Benzyl-N-(/5-methoxy-carbonyloxyäthyl)-amino]-toluol, 3-[N-Benzyl-N-(/3-äthoxy-carbonyl-oxyäthyl)-amino]-toluol, 3-[N-Benzyl-N-(/?-meth-oxyäthyl)-amino]-toluol, 3-[N-Benzyl-N-(/3-äthoxyäthyl)-amino]-toluol, 3-[N-Benzyl-(/3-phenoxyäthyl)-amino]-toluol, 3-[N-Benzyl-N-(/3-phenoxy-acetoxyäthyl)-amino]-toluol, 3-[N-Benzyl-N-(/3-acetylaminoäthyl)-amino]-toluol, 3-[N-Benzyl-N-(y-aeetylaminopropyl)-amino]-toluol, 3-[N-Ben-zyl-N-(^-chloräthyl)-amino]-toluol, 3-[N-Benzyl-N-(/3-di-methylaminoäthyl)-amino]-toluol, 3-[N-Benzyl-N-(y3-di-äthylaminoäthyl)-amino]-toluol, 3-[N-Benzyl-N-(/3-diäthyl-aminoäthyl)-amino]-toluol, 3-[N-Benzyl-N-(y-dimethyl-aminopropyl)-amino]-toluol, 3-[N-Benzyl-N-(/3-hydroxy-äthyl)-amino]-anisol, 3-[N-Benzyl-N-(/3-Cyanäthyl)-amino]-anisol, 3-(N-Benzyl-N-(/3-acetoxyathyl)-aminoJ-anisol, 3-fN-Benzyl-N-(/3-formyloxyäthyl)-amino]-anisol, 3-[N-Benzyl-N-(/3-äthoxycarbonyläthyl)-amino]-anisol, 3-[N-Benzyl-N-(/3-äthoxyearbonyloxyäthyl)-amino]-anisol, 3-[N-Benzyl-N-(/3-methoxyäthyl)-amino]-anisol, 3-[N-Benzyl-N-(/3-phen-oxyäthyl)-amino]-anisol, 3-[N-Benzyl-N-(/3-phenoxyaeetoxy-äthyl)-amino]-anisol, 3-[N-Benzyl-N-(/3-formylaminoäthyl)-aminoj-anisol, 3-[N-BenzyI-N-(y-formyIaminopropyI)-aminoj-anisol, 3-[N-Benzyl-N-(/3-chloräthyl)-amino]-anisol, 3-[N-Benzyl-N-(/3-dimethylaminoäthyl)-amino]-anisol, 3-[N-Benzyl-N-(y-diäthylaminopropyl)-amino]-anisol, 3-[N-Benzyl-N-(/3-hydroxyäthyl)-amino]-acetanilid, 3-[N-Benzyl-N-(jö-cyanäthyl)-amino]-acetanilid, 3-[N-Benzyl-N-(/3-acetoxyäthyl)-amino)-acetanilid, 3-[N-Äthyl-N-(4'-chlorbenzyl)-amino]-toluol, 3-[N-(/3-Cyanäthyl)-N-(4'-ehlorbenzyl)-amino]-toluol, N-(/3-Hydroxyäthyl)-N-(/3-phe-nyläthyl)-anilin, N-(/?-Cyanäthyl)-N-(/i-phenyläthyI)-anilin, N-(/?-Acetoxyäthyl)-N-(/3-phenyläthyl)-anilin, N-(/?-Pro-pionyloxy)-N-(/3-phenyläthyl)-anilin, N-(y3-Methoxycarbonyl-äthyl)-N-(/3-phenyläthyl)-anilin, N-(/3-Äthoxyearbonyläthyl)-N-(/?-phenyläthyl)-anilin, N-(/?-Methoxycarbonyloxyäthy])-N-(/3-phenyläthyl)-anilin, N-(/3-Äthoxycarbonyloxyäthyl)-N-(/3-phenyläthyl)-anilin, N-(/3-Methoxyäthyl)-N-(/3-phenyl-äthyl)-anilin, N-(ß-Äthoxyäthyl)-N-(/3-phenyläthyl)-anilin, N-(/3-Phenoxyäthyl)-N-(/J-phenyläthyl)-anilin, N-(/?-Phen- 3- [N-ethyl-N - (/ 3-phenylethyl) amino] anisole, 3- [N-benzyl-N - (/ 3-phenylethyl) amino] anisole, 3 - [- cyclohexyl-N- (/ 3-phenylethyl) amino] anisole, 3- [N-ethyl-N - (/ 3-phenylethyI) aminoj-acetanilide, 3- [N-benzyl-N - (/? - phenylethyl) - amino] -acetanilide, 3- [N-cyclohexyl-N - (/ 3-phenylethyl) -amino] -acetanilide, N, N-bis- / 3-phenylethyl-aniline, 3- [N, N-bis - (/ ? -Phe-nylethyl) amino] toluene, N - (/ 3-hydroxyethyl) -N-benzyl-aniline, N - (/ S-cyanoethyl) -N-benzyl-aniline, N- (j3-acetoxy-ethyl ) -N-benzyl-aniline, N - (/ 3-propionyloxy) -N-benzyl-aniline, N - (/? - methoxycarbonylethyl) -N-benzyl-aniline, N - (/ 3-ethoxycarbonylethyl) -N -benzyl-aniline, N - (/ 3-methoxycarbonyloxy-ethyl) -N-benzyl-aniline, N - (/ 3-ethoxyearbonyloxyethyl) -N-benzyl-aniline, N - ^ - methoxyethy ^ -N-benzyl-aniline, N- (ß-ethoxyethyl) benzylaniline, N - (/ 3-phenoxyethyl) -N-benzylaniline, N - (/ 3-phenoxyacetoxyethyl) -N-benzylaniline, N- (ß-aeetylaminoethyl) - N-benzyl-aniline, N- (y-acetylaminopropyl) -N-benzyl-aniline, N - (/? - chloroethyl) -N-benzyl-aniline, N - (/ 3-dimethylaminoethyl) -N-benzyl -aniline, N - (/ 3-diethyl-aminoethyl) -N-benzyl-aniline, N- (y-dimethylaminopropyl) -N-benzyl-aniline, 3- [N-benzyl-N - (/ 3-hydroxy-ethyI ) -amino] -toluene, 3- [N-benzyl-N - (/ S-eyanäthyl) -amino] -toluene, 3- [N-BenzyI-N - (/ 3-aeetoxyäthyl) -amino] -toIuol, 3 - [N-benzyl-N - (/? - propionyloxy) amino] toluene, 3- (N-benzyl-N - (/ 3-meth-oxycarbonylethyl) amino] toluene, 3- [N-benzyl- N - (/ 3-ethoxycarbonylethyl) amino] toluene, 3- [N-benzyl-N - (/ 5-methoxycarbonyloxyethyl) amino] toluene, 3- [N-benzyl-N - (/ 3-ethoxy-carbonyl-oxyethyl) amino] toluene, 3- [N-benzyl-N - (/? - meth-oxyethyl) amino] toluene, 3- [N-benzyl-N - (/ 3- ethoxyethyl) amino] toluene, 3- [N-benzyl - (/ 3-phenoxyethyl) amino] toluene, 3- [N-benzyl-N - (/ 3-phenoxy acetoxyethyl) amino] toluene, 3- [N-benzyl-N - (/ 3-acetylaminoethyl) amino] toluene, 3- [N-benzyl-N- (y-aeetylaminopropyl) amino] toluene, 3- [N-benzyl- N - (^ - chloroethyl) amino] toluene, 3- [N-benzyl-N - (/ 3-dimethylaminoethyl) amino] toluene, 3- [N-benzyl-N- (y3-di- ethylaminoethyl) amino] toluene, 3- [N-benzyl-N - (/ 3-diethylaminoethyl) amine o] toluene, 3- [N-benzyl-N- (y-dimethylaminopropyl) amino] toluene, 3- [N-benzyl-N - (/ 3-hydroxyethyl) amino] anisole, 3- [N-benzyl-N - (/ 3-cyanoethyl) amino] anisole, 3- (N-benzyl-N - (/ 3-acetoxyathyl) aminoJ-anisole, 3-fN-benzyl-N- ( / 3-formyloxyethyl) amino] anisole, 3- [N-benzyl-N - (/ 3-ethoxycarbonylethyl) amino] anisole, 3- [N-benzyl-N - (/ 3-ethoxyearbonyloxyethyl) amino] -anisole, 3- [N-benzyl-N - (/ 3-methoxyethyl) -amino] -anisole, 3- [N-benzyl-N - (/ 3-phen-oxyethyl) -amino] -anisole, 3- [ N-benzyl-N - (/ 3-phenoxyethyloxy-ethyl) amino] anisole, 3- [N-benzyl-N - (/ 3-formylaminoethyl) aminoj-anisole, 3- [N-benzyl-N- ( y-FormyIaminopropyI) aminoj-anisole, 3- [N-benzyl-N - (/ 3-chloroethyl) -amino] -anisole, 3- [N-benzyl-N - (/ 3-dimethylaminoethyl) -amino] -anisole , 3- [N-benzyl-N- (y-diethylaminopropyl) amino] anisole, 3- [N-benzyl-N - (/ 3-hydroxyethyl) amino] acetanilide, 3- [N-benzyl-N - (Jo-cyanoethyl) amino] acetanilide, 3- [N-benzyl-N - (/ 3-acetoxyethyl) amino) acetanilide, 3- [N-ethyl-N- (4'-chlorobenzyl) amino ] toluene, 3- [N - (/ 3-cyanoethyl) -N- (4'-chlorobenzyl) - amino] -toluene, N - (/ 3-hydroxyethyl) -N - (/ 3-phe-nylethyl) -aniline, N - (/? - cyanoethyl) -N - (/ i-phenylethyl) -aniline, N- ( /? - acetoxyethyl) -N - (/ 3-phenylethyl) aniline, N - (/? - propionyloxy) -N - (/ 3-phenylethyl) aniline, N- (y3-methoxycarbonyl-ethyl) -N - (/ 3-phenylethyl) aniline, N - (/ 3-ethoxyearbonylethyl) -N - (/? - phenylethyl) aniline, N - (/? - methoxycarbonyloxyethyl]] - N - (/ 3-phenylethyl) aniline , N - (/ 3-ethoxycarbonyloxyethyl) -N - (/ 3-phenylethyl) aniline, N - (/ 3-methoxyethyl) -N - (/ 3-phenylethyl) aniline, N- (ß-ethoxyethyl) -N - (/ 3-phenylethyl) aniline, N - (/ 3-phenoxyethyl) -N - (/ J-phenylethyl) aniline, N - (/? - phen-
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9 9
10 10th
oxyacetoxyäthyl)-N-(/3-phenyläthyl)-anilin, N-(/3-Acetyl-amino-äthyl)-N-(/S-phenyläthyl)-anilin, N-(y-Acetylamino-propyl)-N-(ß-phenyläthyl)-anilin, N-(/3-Chloräthyl)-N-(/3-phenyläthyl)-anilin, N-(/5-Dimethylaminoäthyl)-N-(/3-phe-nyläthyl)-anilin, N-(/S-Diäthylamino-äthyl)-N-(/5-phenyl-äthyl)-anilin, N-(y-Dimethylamino-propyl)-N-(/3-phenyl-äthyl)-anilin, 3-[N-(/3-Phenyl-äthyl)-N-(/3-hydroxy-äthyl)-amino]-toluol, 3-[N-(/3-Phenyl-äthyl)-N-(/3-cyanäthyl)-aminoj-toluol, 3-[N-(/?-Phenyl-äthyl)-N-(/3-acetoxyäthyl)-aminoj-toluol, 3-[N-(/3-Phenyl-äthyl)-N-(/3-propionyloxy)-aminoj-toluol, 3-[N-(/3-Phenyl-äthyl)-N-(/3-methoxycarbo-nyläthyl)-amino]-toluol, 3-[N-(/?-Phenyl-äthyl)-N-(/3-äth-oxycarbonyläthyl)-amino]-toluol, 3-[N-(,8-Phenyl-äthyl)-N-(/S-methoxycarbonyloxyäthyl)-amino]-toluol, 3-[N-(/3-Phenyl-äthyl)-N-(/3-äthoxycarbonyloxyäthyl)-amino]-toluol, 3-[N-(/S-Phenyl-äthyl)-N-(/3-methoxyäthyl)-amino]-toluol, 3-[N-(/S-Phenyl-äthyl)-N-(/S-äthoxyäthyl)-amino]-toluol, 3-[N-(/S-Phenyl-äthyl)-N-(/S-phenoxyäthyl)-amino]-toluol, 3-[N-(/3-Phenyl-äthyl)-N-(/3-phenoxyacetoxy-äthyl)— aminoj-toluol, 3-[N-(/S-Phenyl-äthyl)-N-(/?-acetylamino-äthyl)-amino]-toluol, 3-[N-(/?-Phenyl-äthyl)-N-(y-acetyl-amino-propyl)-amino]-toluol, 3-[N-(/?-Phenyl-äthyl)-N-(/?-chlor-äthyl)-amino]-toluol, 3-[N-Phenyl-äthyl)-N-(/3-di-methylamino-äthyl)-amino]-toluol, 3-[N-(/8-Phenyl-äthyl)-N-(/S-diäthylamino-äthyl)-amino]-toluol, 3-[N-(/S-Phenyl-äthyl)-N-(y-dimethylamino-propyl)-amino]-toluol, 3-[N-(/3-Phenyl-äthyl)-N-(/?-hydroxyäthyl)-amino]-anisol, 3-[N-(/J-Phenyl-äthyl)-N-(ß-cyanäthyl)-amino]-anisol, 3-[N-(/3-Phenyl-äthyl)-N-(/?-acetoxyäthyl)-amino]-anisol, 3-[N-(/3-Phenyl-äthyl)-N-(/?-acetoxy-äthyl)-amino]-anisol, 3-[N-(/3-Phenyl-äthyl)-N-(/?-formyloxyäthyl)-amino]-anisol, 3-[N-(/3-Phenyl-äthyl)-N-(/3-äthoxycarbonyläthyl)-amino]-anisol, 3-[N-(/S-Phenyl-äthyl)-N-(/3-methoxy-äthyl)-amino]-anisol, 3-[N-(/3-Phenyl-äthyl)-N-(/3-phenoxy-äthyl)-amino]-anisol, 3-[N-(/J-Phenyl-äthyl)-N-(/?-phenoxyacetoxy-äthyl)-aminoj-anisol, 3-[N-(/5-Phenyl-äthyl)-N-(/S-formylamino-äthyl)-amino]-anisol, 3-[N-(/S-Phenyl-äthyl)-N-(y-formyl-amino-propyl)-amino]-anisol, 3-[N-(/?-Phenyl-äthyl)-N-(/S-chloräthyl)-amino]-anisol, 3-[N-(/3-Phenyl-äthyl)-N-(/S-di-methylamino-äthyl)-amino]-anisol, 3-[N-(/3-Phenyl-äthyl)-N-(y-diäthylamino-propyl)-amino]-anisol, 3-[N-(/?-Phenyl-äthyl)-N-(/3-hydroxy-äthyl)-amino]-acetanilid, 3-[N-(/3-Phenyl-äthyl)-N-(/3-cyan-äthyl)-amino]-acetanilid, 3-[N-(/3-Phenyl-äthyl)-N-(j0-acetoxy-äthyl)-amino]-acetanilid. oxyacetoxyethyl) -N - (/ 3-phenylethyl) aniline, N - (/ 3-acetylaminoethyl) -N - (/ S-phenylethyl) aniline, N- (y-acetylamino-propyl) -N- (ß-phenylethyl) aniline, N - (/ 3-chloroethyl) -N - (/ 3-phenylethyl) aniline, N - (/ 5-dimethylaminoethyl) -N - (/ 3-phe-nylethyl) aniline, N - (/ S-diethylamino-ethyl) -N - (/ 5-phenyl-ethyl) -aniline, N- (y-dimethylamino-propyl) -N - (/ 3-phenyl-ethyl) aniline, 3- [ N - (/ 3-phenyl-ethyl) -N - (/ 3-hydroxy-ethyl) -amino] toluene, 3- [N - (/ 3-phenyl-ethyl) -N - (/ 3-cyanoethyl) - aminoj-toluene, 3- [N - (/? - phenylethyl) -N - (/ 3-acetoxyethyl) aminoj-toluene, 3- [N - (/ 3-phenylethyl) -N - (/ 3 -propionyloxy) -aminoj-toluene, 3- [N - (/ 3-phenyl-ethyl) -N - (/ 3-methoxycarbo-nylethyl) -amino] -toluene, 3- [N - (/? - phenyl-ethyl ) -N - (/ 3-ethoxycarbonylethyl) amino] toluene, 3- [N - (, 8-phenylethyl) -N - (/ S-methoxycarbonyloxyethyl) amino] toluene, 3- [N - (/ 3-phenylethyl) -N - (/ 3-ethoxycarbonyloxyethyl) amino] toluene, 3- [N - (/ S-phenylethyl) -N - (/ 3-methoxyethyl) amino] - toluene, 3- [N - (/ S-phenylethyl) -N - (/ S-ethoxyethyl) amino] toluene, 3- [N - (/ S-phenylethyl) -N - (/ S- phenoxyethyl) amino] toluene, 3- [N - (/ 3-phenylethyl) -N - (/ 3-phenoxyacetoxyethyl) aminoj-toluene, 3- [N - (/ S-phenylethyl) -N - (/? - acetylamino-ethyl) -amino] -toluene, 3- [N - (/? - phenyl-ethyl) -N- (y-acetylamino-propyl) -amino] -toluene, 3- [N - (/? - phenylethyl) -N - (/? - chloroethyl) amino] toluene, 3- [N-phenylethyl) -N - (/ 3-dimethylaminoethyl) -amino] -toluene, 3- [N - (/ 8-phenyl-ethyl) -N - (/ S-diethylamino-ethyl) -amino] -toluene, 3- [N - (/ S-phenyl-ethyl) - N- (y-dimethylamino-propyl) amino] toluene, 3- [N - (/ 3-phenylethyl) -N - (/? - hydroxyethyl) amino] anisole, 3- [N - (/ J-phenylethyl) -N- (ß-cyanoethyl) amino] anisole, 3- [N - (/ 3-phenylethyl) -N - (/? - acetoxyethyl) amino] anisole, 3- [N - (/ 3-phenyl-ethyl) -N - (/? - acetoxy-ethyl) -amino] anisole, 3- [N - (/ 3-phenyl-ethyl) -N - (/? - formyloxyethyl) -amino] -anisole, 3- [N - (/ 3-phenyl-ethyl) -N - (/ 3-ethoxycarbonylethyl) -amino] -anisole, 3- [N - (/ S-phenyl-ethyl) -N- (/ 3-methoxyethyl) amino] anisole, 3- [N - (/ 3-phenylethyl) -N - (/ 3-phenoxyethyl) amino] anisole, 3- [N- ( / J-phenyl-ethyl) -N - (/? - phenoxyacetoxy-ethyl) -aminoj -anisole, 3- [N - (/ 5-phenyl-ethyl) -N - (/ S-formylamino-ethyl) -amino] -anisole, 3- [N - (/ S-phenyl-ethyl) -N- ( y-formylamino propyl) amino] anisole, 3- [N - (/? - phenylethyl) -N - (/ S-chloroethyl) amino] anisole, 3- [N - (/ 3 -Phenyl-ethyl) -N - (/ S-di-methylamino-ethyl) -amino] -anisole, 3- [N - (/ 3-phenyl-ethyl) -N- (y-diethylamino-propyl) -amino] -anisole, 3- [N - (/? - phenyl-ethyl) -N - (/ 3-hydroxy-ethyl) -amino] -acetanilide, 3- [N - (/ 3-phenyl-ethyl) -N- ( / 3-cyanoethyl) amino] acetanilide, 3- [N - (/ 3-phenylethyl) -N- (j0-acetoxyethyl) amino] acetanilide.
Die Kupplung der Ausgangskomponenten erfolgt in an sich bekannter Weise, beispielsweise in neutralem, saurem oder schwach alkalischem, wässrigem Medium. The starting components are coupled in a manner known per se, for example in neutral, acidic or slightly alkaline, aqueous medium.
Die Quaternierung der Farbstoffe VII erfolgt durch Erwärmen in einem indifferenten organischen Lösungsmittel, z. B. in Kohlenwasserstoffen, wie Benzol, Toluol oder Xylol, Halogenkohlenwasserstoffen, wie Tetrachlorkohlenstoff, Tetrachloräthan, Chlorbenzol, o-Dichlorbenzol, Nitrokohlen-wasserstoffen, wie Nitromethan, Nitrobenzol oder Nitro-naphthalin oder in Dimethylformamid, Acetonitril oder Di-methylsulfoxyd unter Anwendung bevorzugt äquivalenter Mengen alkylierend wirkender Mittel, beispielsweise mit Methylchlorid, Methylbromid, Methyljodid, Äthylbromid, Benzylchlorid, Trimethyloxoniumborfluorid, Dimethylsulfat, Diäthylsulfat, p-Toluolsulfonsäuremethyl-, -äthyl- oder -butyl-ester, Allylbromid, Allylchlorid, Methallylchlorid, Propargyl-chlorid, l,4-Dichlorpropen-2, 2-Chlor-buten-2, 1-Chlor-butin-3, l,2-Dichlorpropen-2, l-Chlor-2-vinyl-propen-2, l-Chlor-pentadien-2,4, Acrylsäure, Acrylsäureamid, Acryl-säuremethyl- oder -äthylester oder Acrylnitril. The quaternization of the dyes VII is carried out by heating in an inert organic solvent, for. Example, in hydrocarbons, such as benzene, toluene or xylene, halogenated hydrocarbons, such as carbon tetrachloride, tetrachloroethane, chlorobenzene, o-dichlorobenzene, nitrocarbons, such as nitromethane, nitrobenzene or nitro-naphthalene or in dimethylformamide, acetonitrile or di-methylsulfonate preferably Amounts of alkylating agents, for example with methyl chloride, methyl bromide, methyl iodide, ethyl bromide, benzyl chloride, trimethyloxonium borofluoride, dimethyl sulfate, diethyl sulfate, p-toluenesulfonic acid methyl, ethyl or butyl ester, allyl bromide, allyl chloride, methallyl chloride, prohalyl chloride, propyl chloride, -Dichloropropene-2, 2-chloro-butene-2, 1-chloro-butyne-3, l, 2-dichloropropene-2, l-chloro-2-vinyl-propene-2, l-chloro-pentadiene-2,4 , Acrylic acid, acrylic acid amide, acrylic acid methyl or ethyl ester or acrylonitrile.
Die Farbstoffe der Formel (I) können durch Lösen in Wasser und Abscheidung durch Zugabe von wasserlöslichen Salzen, beispielsweise Natrium- oder Kaliumchlorid, gereinigt werden. Die so erhaltenen Farbstoffe können nach bekannten The dyes of the formula (I) can be purified by dissolving them in water and separating them by adding water-soluble salts, for example sodium or potassium chloride. The dyes obtained in this way can be prepared using known methods
Austausch-Reaktionen in andere Anionen enthaltende Farbstoffe übergeführt werden. Exchange reactions can be converted into dyes containing other anions.
Die derart erhaltenen Farbstoffe eignen sich hervorragend zum Färben und Bedrucken von kationisch färbbaren textilen s Fasern aus Polymerisaten und Mischpolymerisaten des Acryl-nitrils und des Dicyanäthylens sowie von sauer modifizierten Fasern aus Polyamid und Polyester, wobei echte Farbtöne erhalten werden. The dyes obtained in this way are outstandingly suitable for dyeing and printing cationically dyeable textile fibers made from polymers and copolymers of acrylonitrile and dicyanoethylene, as well as acid-modified fibers made from polyamide and polyester, real colors being obtained.
Es sind bereits kationische Farbstoffe bekannt, und zwar 10 insbesondere aus der FR-PS 1 145 751 und den GB-PS 888 167 und 1 086 994. Gegenüber diesem Stand der Technik ergeben die erfindungsgemäss verwendeten Farbstoffe lichtechtere Färbungen. Cationic dyes are already known, in particular from FR-PS 1 145 751 and GB-PS 888 167 and 1 086 994. Compared to this prior art, the dyes used in accordance with the invention give lightfast dyeings.
Die in der FR-OS 2 019 366 und der DT-OS 2 044 823 15 angegebenen Farbstoffe unterscheiden sich strukturell stärker als diejenigen obiger Veröffentlichungen von den erfindungsgemäss verwendeten Farbstoffen. The dyes specified in FR-OS 2 019 366 and DT-OS 2 044 823 15 differ structurally more than those of the above publications from the dyes used according to the invention.
Zum Färben mit den basischen Farbstoffen der allgemeinen Formeln (I bis IV) gemäss Erfindung eignen sich insbeson-20 dere textile Flocken, Fasern, Fäden, Bänder, Gewebe oder Gewirke aus Polyacrylnitril oder aus mindestens 85% Acryl-nitril-Anteil enthaltenden Mischpolymerisaten des Acryl-nitrils mit anderen Vinylverbindungen, wie Vinylchlorid, Vinylidenchlorid, Vinylfluorid, Vinylacetat, Vinylpyridin, 25 Vinylimidazol, Vinylalkohol, Acryl- und Methacrylsäure-estern und -amiden, as. Dicyanäthylen. Ebenso können Flok-ken, Fasern, Fäden, Bänder, Gewebe oder Gewirke aus sauer modifizierten synthetischen Materialien, insbesondere aus sauer modifizierten Polyamidfasern sowie aus sauer modifi-30 zierten aromatischen Polyestern hervorragend gefärbt werden. Suitable for dyeing with the basic dyes of the general formulas (I to IV) according to the invention are in particular textile flakes, fibers, threads, tapes, fabrics or knitted fabrics made of polyacrylonitrile or of copolymers of acrylic containing at least 85% of acrylonitrile nitriles with other vinyl compounds, such as vinyl chloride, vinylidene chloride, vinyl fluoride, vinyl acetate, vinyl pyridine, 25 vinyl imidazole, vinyl alcohol, acrylic and methacrylic acid esters and amides, as. Dicyanoethylene. Flocks, fibers, threads, tapes, fabrics or knitted fabrics made from acid-modified synthetic materials, in particular from acid-modified polyamide fibers and from acid-modified aromatic polyesters, can also be excellently dyed.
Sauer modifizierte aromatische Polyester sind beispielsweise Polykondensationsprodukte aus Sulfoterephthalsäure und Äthylenglykol, d. h. sulfonsäuregruppenhaltigen Poly-äthylenglykolterephthalaten (Typ DACRON 64 der 35 E. 1. DuPont de Nemours and Company), wie sie in der belgischen Patentschrift 549 179 und der USA-Patentschrift 2 893 816 beschrieben sind. Acid-modified aromatic polyesters are, for example, polycondensation products of sulfoterephthalic acid and ethylene glycol, i.e. H. Polyethylene glycol terephthalates containing sulfonic acid groups (type DACRON 64 of 35 E. 1. DuPont de Nemours and Company), as described in Belgian patent 549 179 and US patent 2 893 816.
Das Färben kann aus schwach saurer Flotte erfolgen, wobei man in das Färbebad zweckmässigerweise bei 40 bis 60° C 40 eingeht und bei Kochtemperatur färbt. Man kann auch unter Druck bei Temperaturen über 100° C färben. Des weiteren lassen sich die Farbstoffe Spinnlösungen zur Herstellung poly-acrylnitrilhaltiger Fasern zusetzen oder auch auf die unver-streckte Faser aufbringen. The dyeing can be carried out from a weakly acidic liquor, the dye bath advantageously being taken in at 40 to 60 ° C. and dyed at the boiling temperature. You can also dye under pressure at temperatures above 100 ° C. Furthermore, the dyes can be added to spinning solutions for the production of polyacrylonitrile-containing fibers or can also be applied to the undrawn fiber.
45 Die Färbungen der Farbstoffe der Formeln (I) bis (IV) auf textile Materialien aus Polyacrylnitril oder sauer modifizierten Polyesterfasern oder Polyamidfasern zeichnen sich durch sehr gute Licht-, Nass-, Reib- und Sublimierechtheit und durch eine hohe Affinität zur Faser aus. Die Farbstoffe 50 sind ausserdem durch ein gutes Ziehvermögen und hohe Ziehgeschwindigkeit ausgezeichnet. 45 The dyeings of the dyes of the formulas (I) to (IV) on textile materials made of polyacrylonitrile or acid-modified polyester fibers or polyamide fibers are characterized by very good light, wet, rubbing and sublimation fastness and by a high affinity for the fiber. The dyes 50 are also distinguished by good drawing power and high drawing speed.
Die Farbstoffe können einzeln oder in Mischungen angewendet werden. Sie sind gut zum Färben von Textilfasern aus Polymerisaten oder Mischpolymerisaten des Acrylnitrils, as. 55 Dicyanäthylens, sauer modifizierten aromatischen Polyestern oder sauer modifizierten synthetischen Superpolyamiden in Chlorkohlenwasserstoffen als Färbebad geeignet, wenn sie die Löslichkeit in Chlorkohlenwasserstoffen fördernde Substituenten, wie z. B. die tert.-Butylgruppe, tragen oder wenn das Anion AnH in den Formeln (I) bis (IV) das Anion einer einbasischen organischen Säure mit 4-30 Kohlenstoffatomen ist. The dyes can be used individually or in mixtures. They are well suited for dyeing textile fibers from polymers or copolymers of acrylonitrile, as. 55 dicyanoethylene, acid-modified aromatic polyesters or acid-modified synthetic superpolyamides in chlorinated hydrocarbons as a dye bath if they improve the solubility in chlorinated hydrocarbons, such as. B. the tert-butyl group, or if the anion AnH in formulas (I) to (IV) is the anion of a monobasic organic acid with 4-30 carbon atoms.
Derartige organische Säuren sind beispielsweise: Such organic acids are for example:
2-Äthylcapronsäure, Laurinsäure, Ölsäure, Linolsäure, ein Gemisch aliphatischer Carbonsäuren mit 15-19 Kohlenstoffatomen (Versatic-Säure 1519), ein Gemisch aliphatischer Carbonsäuren mit 9-11 Kohlenstoffatomen (Versatic-Säure 911), Kokosfettsäurevorlauf, Tetradecansäure, Undecylen- 2-ethylcaproic acid, lauric acid, oleic acid, linoleic acid, a mixture of aliphatic carboxylic acids with 15-19 carbon atoms (Versatic acid 1519), a mixture of aliphatic carboxylic acids with 9-11 carbon atoms (Versatic acid 911), coconut fatty acid feed, tetradecanoic acid, undecylene-
11 11
12 12
säure, Dimethylpropansäure, Dimethylessigsäure, Carbonsäuren, deren Kohlenstoffkette durch Heteroatome unterbrochen ist, wie Nonylphenoltetraäthylenglykolätherpropion-säure, Nonylphenoldiäthylenglykolätherpropionsäure, Dode-cyltetraäthylenglykolätherpropionsäure, 3-(Nonyloxy)-pro-pionsäure, 3-(lsotridecyloxy)-propionsäure, 3-(Isotridecyl-oxy)-diäthylenglykolätherpropionsäure, Ätherpropionsäure des Alkoholgemisches mit 6-10 Kohlenstoffatomen, Nonyl-phenoxyessigsäure, aromatische Carbonsäuren, wie tert.-Butylbenzoesäure, cycloaliphatische Carbonsäuren, wie Hexa-hydrobenzoesäure, Cyclohexencarbonsäure, Abietinsäure und Sulfonsäuren. wie Tetrapropylenbenzolsulfonsäure. acid, dimethylpropanoic acid, dimethylacetic acid, carboxylic acids, the carbon chain of which is interrupted by heteroatoms, such as nonylphenol tetraethylene glycol ether propionic acid, nonylphenol diethylene glycol propionic acid, dode-cyltetraethylene glycol ether propionic acid, 3- (nonyloxy) propyl acid, 3- (nonyloxy) propyl acid, 3- (pyloxy) propyl acid, 3- (pyloxy) propyl acid, 3- (pyloxy) propyl acid, 3- (pyloxy) propyl acid, 3- (pyloxy) propyl acid, ) -Diethylenglykolätherpropionsäure, ether propionic acid of the alcohol mixture with 6-10 carbon atoms, nonyl-phenoxyacetic acid, aromatic carboxylic acids such as tert-butylbenzoic acid, cycloaliphatic carboxylic acids, such as hexa-hydrobenzoic acid, cyclohexenecarboxylic acid, abietic acid and sulfonic acids. such as tetrapropylene benzene sulfonic acid.
In den folgenden Beispielen bedeuten Teile Gewichtsteile. In the following examples, parts mean parts by weight.
Beispiel 1 example 1
93,5 Teile 1 -Phenyl-3,4-dimethyl-5-amino-pyrazol werden unter Rühren in 600 Teile Orthophosphorsäure eingetragen und anschliessend durch Zutropfen von 158 Teilen 41,8%iger Nitrosylschwefelsäure im Verlaufe von etwa 1 Stunde bei 0-3° C diazotiert. Durch zweistündiges Nachrühren bei 0-3 °C wird die Diazotierung zu Ende geführt. Um überschüssige 93.5 parts of 1-phenyl-3,4-dimethyl-5-amino-pyrazole are introduced into 600 parts of orthophosphoric acid with stirring and then by dropwise addition of 158 parts of 41.8% nitrosylsulfuric acid over the course of about 1 hour at 0-3 ° C diazotized. The diazotization is brought to an end by stirring at 0-3 ° C. for two hours. To excess
Nitrosylschwefelsäure zu zerstören, werden anschliessend 5 Teile Harnstoff zugefügt und weitere 30 Minuten gerührt. Die so hergestellte Diazoniumsalzlösung gibt man unter Rühren zu einer Mischung aus 1 13 Teilen 3-(N-Äthyl-N-benzyl-5 amino)-toluol, 1000 Teilen Wasser und 2000 Teilen Eis. Nach 5~6stündigem Rühren ist die Kupplung beendet. Der entstandene Farbstoff wird auf der Nutsche abfiltriert und dreimal mit jeweils 500 Teilen Wasser gewaschen. Nach anschliessender Trocknung erhält man 195 Teile Farbstoff in Form io eines orangefarbenen Pulvers. Dieser Farbstoff wird in 2225 Teile Chlorbenzol eingetragen und auf 100° C erhitzt. Bei dieser Temperatur werden im Verlaufe von 1-2 Stunden 63 Teile Dimethylsulfat zugetropft. Dann wird so lange bei 120°C nachgerührt, bis im Dünnschichtchromatogramm kein 15 Ausgangsfarbstoff mehr nachweisbar ist. Darauf wird auf Raumtemperatur abgekühlt und der auskristallisierte Farbstoff abfiltriert. Er wird mit Chlorbenzol nachgewaschen und bei 60° C getrocknet. Man erhält 240 Teile dunkelrotes Farbstoffpulver, das sich mit roter Farbe in Wasser löst. Der Farb-20 stoff hat mit grosser Wahrscheinlichkeit die folgende Konstitution: To destroy nitrosylsulfuric acid, 5 parts of urea are then added and the mixture is stirred for a further 30 minutes. The diazonium salt solution thus prepared is added with stirring to a mixture of 1 13 parts of 3- (N-ethyl-N-benzyl-5 amino) toluene, 1000 parts of water and 2000 parts of ice. After stirring for 5 ~ 6 hours, the coupling is complete. The resulting dye is filtered off on a suction filter and washed three times with 500 parts of water each time. After drying, 195 parts of dye are obtained in the form of an orange powder. This dye is added to 2225 parts of chlorobenzene and heated to 100 ° C. At this temperature, 63 parts of dimethyl sulfate are added dropwise in the course of 1-2 hours. The mixture is then stirred at 120 ° C. until the starting dye is no longer detectable in the thin layer chromatogram. It is then cooled to room temperature and the dyestuff which has crystallized out is filtered off. It is washed with chlorobenzene and dried at 60 ° C. 240 parts of dark red dye powder are obtained, which dissolves in water with red paint. It is very likely that the dye 20 has the following constitution:
V » V »
/C2 H8 / C2 H8
CH, CH,
CH, SO, CH, SO,
27,5 Teile dieses Farbstoffes werden unter Erwärmen in 30 versetzt. Das ausfallende Farbstoffpulver wird durch Filtration 500 Teilen Wasser gelöst und mit der Lösung von 8 Teilen isoliert. Man erhält nach dem Trocknen 29 Teile des Farb- 27.5 parts of this dye are added to 30 with heating. The precipitated dye powder is dissolved by filtration 500 parts of water and isolated with the solution of 8 parts. After drying, 29 parts of the color
Zinkchlorid und 10 Teilen Natriumchlorid in 50 Teilen Wasser stoffs der wahrscheinlichen Konstitution: Zinc chloride and 10 parts sodium chloride in 50 parts hydrogen of the likely constitution:
h3c ch„ h3c ch "
✓C2He ✓C2He
Ò 04 Ò 04
ZnCl, ZnCl,
0,1 Teil des ursprünglich erhaltenen Farbstoffs mit CH,S04® als Anion bzw. 0,1 Teil des in einer Folgereaktion erhaltenen Farbstoffs mit ZnCl.,© als Anion werden in 50 Teilen Wasser unter Erwärmen gelöst und mit 0,5-2 Teilen «Avolan IS» (Kondensationsprodukt aus Naphthalinsulfon-säure und Formaldehyd) versetzt. Mit kaltem Wasser wird sodann auf 500 Teile aufgefüllt und mit Essigsäure wird der pH-Wert auf 4,5-5 eingestellt. In diese Färbeflotte geht man mit 10 Teilen Polyacrylnitrilfasern oder sauer modifizierten Polyamidfasern (z. B-Dye I) (als Stückware oder Garn) ein und erhitzt innerhalb von 30 Minuten auf 100° C. Bei dieser Temperatur färbt man 60 Minuten. Dann wird das Material mit kaltem Wasser gründlich gespült und bei 60-70° C getrocknet. Man erhält eine klare Rotfärbung, die ausgezeichnete Echtheiten aufweist. 0.1 part of the dye originally obtained with CH, S04® as the anion or 0.1 part of the dye obtained in a subsequent reaction with ZnCl., © as the anion are dissolved in 50 parts of water with heating and with 0.5-2 parts "Avolan IS" (condensation product of naphthalenesulfonic acid and formaldehyde) added. The mixture is then made up to 500 parts with cold water and the pH is adjusted to 4.5-5 with acetic acid. This dye liquor is mixed with 10 parts of polyacrylonitrile fibers or acid-modified polyamide fibers (for example Dye I) (as piece goods or yarn) and heated to 100 ° C. in the course of 30 minutes. Dyeing for 60 minutes. Then the material is rinsed thoroughly with cold water and dried at 60-70 ° C. A clear red color is obtained which has excellent fastness properties.
Für das Färben von sauer modifizierten Polyglykoltere-phthalatfasern (Typ «Dacron 64») erfolgt zur Färbeflotte noch ein Zusatz eines Carriers, z. B. von 1-3 Teilen eines aromatischen Oxycarbonsäureesters oder Diphenyls. Auch in diesem Falle erhält man eine Rotfärbung mit hervorragenden Echtheitseigenschaften. For dyeing acid-modified polyglycol terephthalate fibers (type «Dacron 64»), a carrier is added to the dyeing liquor, e.g. B. 1-3 parts of an aromatic oxycarboxylic acid ester or diphenyl. In this case too, a red color is obtained with excellent fastness properties.
45 Der Farbstoff des Beispiels 1 kann auch im Druck Verwendung finden. Dazu wird ein Gewebe aus Polyacrylnitril mit einer folgendermassen hergestellten Druckpaste bedruckt: 30 Teile Farbstoff, 50 Teile Thiodiäthylenglykol, 30 Teile Cyclohexanol und 30 Teile 30%ige Essigsäure werden mit 330 so Teilen heissem Wasser vermischt und die Lösung zu 500 Teilen Kristallgummi gegeben. Zu dieser Druckpaste werden noch 30 Teile Zinknitratlösung zugesetzt. 45 The dye of Example 1 can also be used in printing. For this purpose, a fabric made of polyacrylonitrile is printed with a printing paste prepared as follows: 30 parts of dye, 50 parts of thiodiethylene glycol, 30 parts of cyclohexanol and 30 parts of 30% acetic acid are mixed with 330 parts by weight of hot water and the solution is added to 500 parts of crystal rubber. 30 parts of zinc nitrate solution are added to this printing paste.
Nach dem Bedrucken wird das Gewebe getrocknet, 30 Minuten gedämpft und anschliessend gespült. Man erhält einen 55 roten Druck mit sehr guten Echtheitseigenschaften. After printing, the fabric is dried, steamed for 30 minutes and then rinsed. A 55 red print with very good fastness properties is obtained.
Weitere erfindungsgemäss verwendete Farbstoffe, die Färbungen mit hervorragenden Echtheitseigenschaften liefern, sind in der nachfolgenden Tabelle aufgeführt: Further dyes used according to the invention, which provide dyeings with excellent fastness properties, are listed in the table below:
6469/73 6469/73
2 2nd
3 3rd
4 4th
5 5
6 6
7 7
8 8th
9 9
10 10th
11 11
13 13
14 14
Diazokomponente Kupplungskomponente Ouaternierungsmittel n*0 Diazo component coupling component ouating agent n * 0
o-"1*. o o- "1 *. o
ô O
ch3 Cl ch3 Cl
ç^-NHCHg ocha ç ^ -NHCHg ok
% %
chch,-© chch, - ©
/7~\ /C2H5 / 7 ~ \ / C2H5
/""A /C4K» / "" A / C4K »
chch, .0 chch .0
/CH2 "^3 / CH2 "^ 3
/(«) ^h*-© / («) ^ H * - ©
(CH30)2S02 (CH30) 2S02
(CH,0)2S02 (CH, 0) 2S02
(CH30)2S02 (CH30) 2S02
(CH30)2S02 (CH30) 2S02
(CH30)2S02 (CH30) 2S02
(CH,0)2S02 (CH, 0) 2S02
/-Tv / ^3 / -Tv / ^ 3
W ^ (CH.OfcSO, W ^ (CH.OfcSO,
(CH30)2S02 (CH30) 2S02
(CH30)2S02 (CH30) 2S02
(CH30)2S02 (CH30) 2S02
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12 12
13 13
14 14
15 15
16 16
17 17th
18 18th
19 19th
20 20th
21 21st
15 15
16 16
Diazokomponente Kupplungskomponente Ouaternierungsmittel Diazo component Coupling component Ouaternizing agent
ô O
f>ncks f> ncks
\=/ n \ = / n
NSHj -^^-NOg NSHj - ^^ - NOg
OC-q OC-q
NOj NOj
'CH® 'CH®
.ch. .ch.
ch, ch,
jT~\ ✓C*H» jT ~ \ ✓C * H »
^ V -Q ^ V -Q
Cl Cl
>=/ > = /
OC Ks x=y OC Ks x = y
(CH30)2S02 (CH30) 2S02
(CH30)2S02 (CH30) 2S02
(CH30)2S02 (CH30) 2S02
(Q-nhch, CH, (Q-nhch, CH,
^^-NHCHa c^5 ^^ - NHCHa c ^ 5
/TÄ /CaH8 / TÄ / CaH8
(CH30)2S02 (CH30) 2S02
(CH30)2S02 (CH30) 2S02
(CH30)2S02 (CH30) 2S02
H* V (C2Hs0)2S02 H * V (C2Hs0) 2S02
NHCOCHj NHCOCHj
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17 17th
18 18th
Beispiel Diazokomponente Kupplungskomponente Example diazo component coupling component
Quaternierungsmittel Quaternizing agent
Farbton auf Polyacrylnitril Color on polyacrylonitrile
22 22
23 23
24 24th
«.c CH, «.C CH,
ò O
ocn, ocn,
■kn/c'h' ■ kn / c'h '
nch, nch,
CH3 <=/ CH3 <= /
OCI OCI
H. H.
// v X - // v X -
OCH. \=/ OCH. \ = /
OCHb OCI OCHb OCI
NHCOC, H8 NHCOC, H8
;H5. ; H5.
_AH« _AH"
(C2H50)2S02 (C2H50) 2S02
(C2Hs0)2S02 (C2Hs0) 2S02
(c2h5o)2so2 (c2h5o) 2so2
blaust. Rot blaust. Rot blaust. Rot bluish. Red bluish. Red bluish. red
25 25th
y\{} y \ {}
CH;, CH ;,
(C2H50)2S02 (C2H50) 2S02
Rot red
26 26
w <CH, w <CH,
C2H5Br gelbst. Rot C2H5Br yellow. red
27 27th
28 28
.CIL CiL OH .CIL CiL OH
°vo ° vo
C2H5Br C2H5Br
C,H,Br gelbst. Rot gelbst. Rot C, H, Br yellow. Red yellow. red
29 29
30 30th
31 31
/CHg CH. NHCOCH* / CHg CH. NHCOCH *
<>/ <> /
\=J V \ = J V
ÇH, ÇH,
CK, CH, NHSO, CK, CH, NHSO,
c«,^> c «, ^>
o» O"
\=/ \, \ = / \,
NHg NHg
/CH, CH, NHCO / CH, CH, NHCO
?CH,0 ? CH, 0
C2H,Br C2H, Br
QHsBr QHsBr
C2HsBr gelbst. Rot gelbst. Rot gelbst. Rot C2HsBr yellow. Red yellow. Red yellow. red
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19 19th
20 20th
Beispiel Diazokomponente Kupplungskomponente Ouaternierungsmittel Farbton auf Example Diazo component Coupling component Ouaternierungsmittel color
Polyacrylnitril Polyacrylonitrile
H»C CHg /T~\ H »C CHg / T ~ \
» ÄH, -er o ~ »UH, -er o ~
,0h, ch. raco-f^a , 0h, ch. raco-f ^ a
33 — C2HsBr §elbst Rot 33 - C2HsBr §elbst Rot
34 34
36 36
/"TX/C^i CH, 0C0CH / "TX / C ^ i CH, 0C0CH
\=-S~\JH, (CH30)2S02 gelbst. Rot \ = - S ~ \ JH, (CH30) 2S02 yellow. red
>7-rv /CH. CIL OCKL CH. OH > 7-rv / CH. CIL OCKL CH. OH
^h,-0 ^ h, -0
35 (CH30)2S02 gelbst. Rot 35 (CH30) 2S02 yellow. red
^ /CHjCHjOCOOC^ ^ / CHjCHjOCOOC ^
(/ \Vn /—n (CH30)2S02 gelbst. Rot (/ \ Vn / —n (CH30) 2S02 yellow. Red
WYh.HQ WYh.HQ
/CH, CH^ OCH, / CH, CH ^ OCH,
37 - v 7"^ /r~\ (CH30)2S02 gelbst. Rot 37 - v 7 "^ / r ~ \ (CH30) 2S02 yellow. Red
/TTy w-"xcn -0 / TTy w- "xcn -0
~,C*C*O0 ~, C * C * O0
voh»-Ö> voh »-Ö>
38 „ - // \v»/ "* "jl, v=v (CH30)2S02 gelbst. Rot ok 38 "- // \ v» / "*" jl, v = v (CH30) 2S02 yellow. Red ok
/CI^CH,C00Cïfc ci4"Ô / CI ^ CH, C00Cïfc ci4 "Ô
39 ^ x> n /—\ (CH30)2S02 gelbst. Rot ck 39 ^ x> n / - \ (CH30) 2S02 yellow. Red ck
C^CHjSOJCI^ C ^ CHjSOJCI ^
CH,-0 CH, -0
fAif HJCHjSOI -0> fAif HJCHjSOI -0>
o^<0> o ^ <0>
40 (CH30)2S02 gelbst. Rot 40 (CH30) 2S02 yellow. red
(CH30)2S02 gelbst. Rot (CH30) 2S02 yellow. red
6469/73 6469/73
Bei At
42 42
43 43
44 44
45 45
46 46
47 47
48 48
49 49
50 50
51 51
21 21st
22 22
Diazokomponente Kupplungskomponente Diazo component coupling component
Quaternierungsmittel Quaternizing agent
*CWC* * CWC *
0 0
CK CK
/CHa CH, Cl / CHa CH, Cl
CH.-0 CH.-0
(CH30)2S02 (CH30) 2S02
^ ✓CH,CH,CH,C1 ^ ✓CH, CH, CH, C1
(CH30)2S02 (CH30) 2S02
,CH,CH,OCOOH.-0 , CH, CH, OCOOH.-0
(CH30)2S02 (CH30) 2S02
^ ,CH, CH, 0C0N(CHb ), ^, CH, CH, 0C0N (CHb),
O^ch, -A <ch,0,'s°! O ^ ch, -A <ch, 0, 's °!
/OH, CH.CN / OH, CH.CN
e nvn e nvn
^"CH, -qci ^ "CH, -qci
(CH30)2S02 (CH30) 2S02
™ /CH, CH, CN (/ \>N ^ ™ / CH, CH, CN (/ \> N ^
^ sch,^3 ^ sch, ^ 3
NO, NO,
,(CH, WC,»,), , (CH, WC, »,),
(CH3o)2so2 (CH3o) 2so2
(CH,0)2S02 (CH, 0) 2S02
/CI^ CH, OCONH-^^ / CI ^ CH, OCONH - ^^
>=/ (CH30)2S02 > = / (CH30) 2S02
ch.-0 ch.-0
(^3"MH-CH, CK, -<Q) (^ 3 "MH-CH, CK, - <Q)
Cl Cl
(CH30)2S02 (CH30) 2S02
/t~\ /caH» / t ~ \ / caH »
CHj ' W CHj'W
(CH30)2S02 (CH30) 2S02
6469/73 6469/73
23 23
24 24th
Beispiel Diazokomponente Example diazo component
Kupplungskomponente Coupling component
Ouaternierungsmittel Ouaternizing agent
Farbton auf Polyacrylnitril Color on polyacrylonitrile
52 52
53 53
HC. ÇH. HC. ÇH.
N^-nh, 0-N N ^ -nh, 0-N
Ô O
CH.CH "O CH.CH "O
vCHj CHg ch,ci ch,c1 vCHj CHg ch, ci ch, c1
gelbst. Rot gelbst. Rot yellow. Red yellow. red
54 54
~^ ch. ch. cn \=/ "^clij ch. -^3 ~ ^ ch. ch. cn \ = / "^ clij ch. - ^ 3
ch,c1 ch, c1
gelbst. Rot yellow. red
55 55
56 56
H' H'
>=/ 'CH.CH,-^__^ Hp-QaD^CH, > = / 'CH.CH, - ^ __ ^ Hp-QaD ^ CH,
NHCOCHj NHCOCHj
P». P ».
3HS 3HS
^CHa' ^ CHa '
blaust. Rot bluish. red
Rot red
57 57
rvch°c>5n w -c^o rvch ° c> 5n w -c ^ o
Rot red
58 58
? xVn ? xVn
/ ci^ ch2 oh / ci ^ ch2 oh
ÎH3 ÎH3
C«2"0 C «2" 0
Rot red
59 59
/-ch,ch,n(cih, ), / -ch, ch, n (cih,),
Rot red
60 60
r—v ✓ch.ch.nhcho CHg X=/ r — v ✓ch.ch.nhcho CHg X = /
Rot red
6469/73 6469/73
25 25th
26 26
Beispiel Diazokomponente Kupplungskomponente Ouaternierungsmittel Farbton auf Example Diazo component Coupling component Ouaternierungsmittel color
Polyacrylnitril Polyacrylonitrile
H.C CH, H.C CH,
■$->«. ©■"Cïy?'™' »o« >-ò * ■ $ -> «. © ■ "Cïy? '™'» o «> -ò *
^CH^ CH, NHSQ, Ca Hj ^ CH ^ CH, NHSQ, Ca Hj
62 „ r-rv ' „ Rot 62 "r-rv '" red
« ^ CH.CMmCONHC^ «^ CH.CMmCONHC ^
^ SCK, O CH, ^ SCK, O CH,
j-r* ,CH,CH,NHC0-£\CH, j-r *, CH, CH, NHC0- £ \ CH,
p^-o r*j \=/ p ^ -o r * j \ = /
64 ,, Rot 64 ,, red
CH- CH-
/7~\ /CHac*^ OCOCj|Ha / 7 ~ \ / CHac * ^ OCOCj | Ha
65 „ // \>m' __ „ Rot 65 "// \> m '__" Red
<r <r
66 „ (/ nVh . „ Rot 66 "(/ nVh." Red
PAn»l'nï ^ CH, X=y PAn »l'nï ^ CH, X = y
P^C^OCC P ^ C ^ OCC
. 'uo . 'uo
L. . H« V"l L.. H "V" l
,C H, Ci^ OCOOCf^ , C H, Ci ^ OCOOCf ^
67 „ V V$ /7-rv „ Rot 67 "V V $ / 7-rv" Red
-Cl -Cl
» v r »V r
CH, CH,
-CHj CHj OCH, -CHj CHj OCH,
68 " V__7NV /n\ (CH30)2S02 Rot 68 "V__7NV / n \ (CH30) 2S02 red
CH-Ô CH-Ô
ch, w ch, w
/r^\ /CHaCHaO-0) / r ^ \ / CHaCHaO-0)
ovo ovo
~>U \=/ ~> U \ = /
69 (CH30)2S02 Rot 69 (CH30) 2S02 red
CHs CHs
6469/73 6469/73
27 27th
28 28
Beispiel Diazokomponente Kupplungskomponente Ouaternierungsmittel Farbton auf Example Diazo component Coupling component Ouaternierungsmittel color
Polyacrylnitril chö Polyacrylonitrile
/CHj CHj COOCj H8 / CHj CHj COOCj H8
70 (/ XVN Ä-Ä (CH30)2S02 Rot 70 (/ XVN Ä-Ä (CH30) 2S02 Red
/CH-C^CO / CH-C ^ CO
0 e* 0 e *
/CHtCHtS0||-O / CHtCHtS0 || -O
(CH,0)2S02 Rot (CH, 0) 2S02 red
— /CUCICI - / CUCICI
72 „ (' N>N >7-^ (CH30)2S02 Rot 72 „('N> N> 7- ^ (CH30) 2S02 red
CHa x-/ CHa x- /
/CHtCH2CHtBr / CHtCH2CHtBr
73 „ (' 7-N (CH30)2S02 Rot 73 "('7-N (CH30) 2S02 Red
>=/ nCH8'V >Br ck, > = / nCH8'V> Br ck,
,CH. CH, OCOCHfO , CH. CH, OCOCHfO
sx, <3 ^ sx, <3 ^
CH3 W CH3 W
74 74
n /—V (CH30)2S02 Rot n / —V (CH30) 2S02 red
—, ^CHjOCONCCH )f CH3 ^ -, ^ CHjOCONCCH) f CH3 ^
75 V Z1? — /T^ (CH30)2S02 Rot 75 V Z1? - / T ^ (CH30) 2S02 red
„ /CH-CH-OÖp.NCCHt )a "/CH-CH-OÖp.NCCHt) a
76 // \\m * * ^ * (CH30)2S02 Rot 76 // \\ m * * ^ * (CH30) 2S02 red
/TT\ / TT \
pvo ch3 w pvo ch3 w
^ xCHj CHg CN ^ xCHj CHg CN
,PVO< , PVO <
^CI^CHgCN ^ CI ^ CHgCN
77 V^_V"Nv (CH30)2S02 Rot 77 V ^ _V "Nv (CH30) 2S02 red
3Ha " 3Ha "
/CH, ),N(CH, ), / CH,), N (CH,),
78 v N >7-^, (CH30)2S02 Rot pvo 78 v N> 7- ^, (CH30) 2S02 red pvo
,CH, CH OCONH-^^-tl , CH, CH OCONH - ^^ - tl
->w_ \=y -> w_ \ = y
79 (CH30)2S02 Rot 79 (CH30) 2S02 red
6469/73 6469/73
29 29
30 30th
Beispiel Diazokomponente Example diazo component
Kupplungskomponente Coupling component
Quaternierungsmittel Quaternizing agent
Farbton auf Polyacrylnitril Color on polyacrylonitrile
80 80
81 81
82 82
HjCCHj HjCCHj
ó O
CH3 CH3
Q-nhch-0» Q-nhch-0 »
OC Ha OC Ha
^JVNHCH, CHa Cl ^ JVNHCH, CHa Cl
{ysopc^ {ysopc ^
Orange rotst. Orange Orange red. orange
Orange orange
83 83
84 84
85 85
86 86
87 87
89 89
CHg CHg
CH3 CH3
och3 och3
ç^nxch,chi-0 ç ^ nxch, chi-0
W W
>=/ N3H.CH, -<H> CHj > = / N3H.CH, - <H> CHj
/T^\ /CH, CHa CN >=' Nn CHg CHj / T ^ \ / CH, CHa CN> = 'Nn CHg CHj
CHj ^ CHj ^
OCHb /r^. /CfH5 OCHb / r ^. / CfH5
p^CH.^ p ^ CH. ^
CH, ^ CH, ^
pvcha^ pvcha ^
VU ^ VU ^
<0CH,C1 <0CH, C1
Orange rotst. Orange Orange red. orange
Rot red
Rot red
Rot blaust. Rot blaust. Rot Red bluish. Red bluish. red
OCB OCB
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31 31
32 32
Beispiel Diazokomponente Kupplungskomponente Example diazo component coupling component
Ouaternierungsmittel Ouaternizing agent
Farbton auf Polyacrylnitril Color on polyacrylonitrile
Hb C CH# Hb C CH #
90 NÎ'VNH, 90 NÎ'VNH,
lì lì
0cahs 0cahs
>c2h8 > c2h8
nhcochs nhcochs
blaust. Rot bluish. red
91 91
>=/ ^ch, CH, ei N=/ > = / ^ ch, CH, ei N = /
Rot red
92 92
7 vs 7 vs
(CH3o)2so2 (CH3o) 2so2
rotst. Orange red orange
93 93
94 94
0-nhch,-<q 0-nhch, - <q
CH. CH.
0-nhch.-0 0-no
Cl Cl
(CH30)2S02 (CH30) 2S02
(ch3o)2so2 (ch3o) 2so2
Rot red
Rot red
95 Ç^-NHCH, (CH30)2S02 Rot 95 Ç ^ -NHCH, (CH30) 2S02 red
OC Hb ck ch-0 OC Hb ck ch-0
96 CH2=CH—CH2C1 gelbst. Rot 96 CH2 = CH-CH2C1 yellow. red
'C»H, 'C »H,
97 „ // VVîî /—% CH2=CH-CH2C1 gelbst. Rot 97 „// VVîî / -% CH2 = CH-CH2C1 yellow. red
©co oc © co oc
/c.h, /c.h,
=h."0 = h. "0
98 CH2=CH—CH2C1 gelbst. Rot 98 CH2 = CH-CH2C1 yellow. red
99 99
oc-o oc-o
6469/74 6469/74
CH2=CH-CH2C1 CH2 = CH-CH2C1
gelbst. Rot yellow. red
Beis By S
100 100
101 101
102 102
103 103
104 104
105 105
106 106
107 107
108 108
109 109
33 33
34 34
Diazokomponente Kupplungskomponente Ouaternierungsmittel Diazo component Coupling component Ouaternizing agent
HgC, CHi HgC, CHi
ò O
x«> x «>
/B-T\ /-CH, / B-T \ / -CH,
0-nsch,-qci o^yv 0-nsch, -qci o ^ yv
/7~\ /CtHB / 7 ~ \ / CtHB
ckh.-Q ckh.-Q
NO, NO,
CH., CH.,
fVc,H' fVc, H '
\=/ srH.fîi \ = / srH.fîi
.CH, .CH,
►■n ► ■ n
CH, CH,
/"A .CH, / "A .CH,
o" v <3 o "v <3
flH- flH-
f^-n f ^ -n
A«, A «,
^ ^ o ^ ^ o
Cl ch2=ch-ch,c1 Cl ch2 = ch-ch, c1
(ch3o)2so2 (ch3o) 2so2
(ch30)2s02 (ch30) 2s02
(ch30)2s02 (ch30) 2s02
(ch30)2s02 (ch30) 2s02
0-NHCHCH.-0 ¥-0 S020CH5 0-NHCHCH.-0 ¥ -0 S020CH5
(ch3o)2so2 (ch3o) 2so2
(ch30)2s02 (ch30) 2s02
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Beis By S
110 110
111 111
112 112
113 113
114 114
115 115
116 116
117 117
118 118
119 119
35 35
36 36
Diazokomponente Kupplungskomponente Quaternierungsmittel h5cu çh oc ha Diazo component coupling component quaternizing agent h5cu çh oc ha
<rvCsH»^ <rvCsH »^
nhcochg och,, nhcochg och ,,
fi.«'0'** fi. «'0' **
w VCHs^) CHa X==y oc h, w VCHs ^) CHa X == y oc h,
//-«An. //-"At.
)=/ ) = /
ochg x=/ ochg x = /
/~^K--V2"5 / ~ ^ K - V2 "5
cH**0 cH ** 0
nhcoc2 h6 x=y nhcoc2 h6 x = y
CHg v-/ CHg v- /
/chg ch, cn / chg ch, cn
^ v -q ^ v -q
^chg ch, oh ^ chg ch, oh
,CV* , CV *
/-»v ch,ch,it fv /T\ CK» / - »v ch, ch, it fv / T \ CK»
xCHg xCHg
^chg ch, nhcoch3 ^ chg ch, nhcoch3
(CH30)2S02 (CH30) 2S02
(C2h5o)2so2 (C2h5o) 2so2
(c2h5o)2so2 (c2h5o) 2so2
(C2H50)2S02 (C2H50) 2S02
och3 och3
C2hs vn -T-'V. (C2H50)2S02 C2hs vn -T-'V. (C2H50) 2S02
^ A H» ^ A H »
</ X>N /—-rv (C2H,0)2S02 </ X> N / - rv (C2H, 0) 2S02
C2HcBr C2HcBr
C2H,Br C2H, Br
C2H5Br C2H5Br
C2H5Br C2H5Br
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38 38
Beispiel Diazokomponente Kupplungskomponente Quaternierungsmittel Farbton auf Example diazo component coupling component quaternizing agent color
Polyacrylnitril hsc- chg ^ Polyacrylonitrile hsc- chg ^
v_y /ch, ch, nhsoj v_y / ch, ch, nhsoj
120 1V«X>NH. (f ^VN C2H5Br gelbst. Rot v—< /—v /in. «rwv« 120 1V «X> NH. (f ^ VN C2H5Br yellow. Red v— </ —v / in. «rwv«
n^mh, q« ^ © n ^ mh, q «^ ©
nh, nh,
/t^\ /ch, ch, nhco / t ^ \ / ch, ch, nhco
121 „ \=l/ \ C2H5Br gelbst. Rot 121 "\ = l / \ C2H5Br yellow. red
^ ch.ch.nhc°-0 ^ ch.ch.nhc ° -0
vcha-^) vcha- ^)
122 ^ ' y-N /"""TV ' C2H5Br gelbst. Rot 122 ^ 'y-N / "" "TV' C2H5Br yellow. Red
/ ch® ch, nhco-^~^vcq / ch® ch, nhco- ^ ~ ^ vcq
123 „ ;/ Wj^ \=/ C2H5Br gelbst. Rot 123 „; / Wj ^ \ = / C2H5Br yellow. red
"chj "chj
/7-a /chj ch, ococh^j / 7-a / chj ch, ococh ^ j
124 „ V X>-N /r—v (CH,0)2S02 gelbst. Rot vch2"C=y 124 "V X> -N / r - v (CH, 0) 2S02 yellow. Red vch2 "C = y
^h, ch, och, ch, oh ^ h, ch, och, ch, oh
125 ^=>v fi ^ (CH30)2S02 gelbst. Rot 125 ^ => v fi ^ (CH30) 2S02 yellow. red
Ö/c^chgocoochs Ö / c ^ chgocoochs
»N t ». (CH30)2S2 gelbst. Rot "N t". (CH30) 2S2 yellow. red
'ch. <^3 'ch. <^ 3
127 „ (CH,0),S0, gelbst. Roi 127 "(CH, 0), S0, yellow. Roi
,Ç-\ /clichjo , Ç- \ / clichjo
128 „ \s=y"N\ (CH30)2S02 gelbst. Rot ncha w r-* /ch, ch, coochg 128 "\ s = y" N \ (CH30) 2S02 yellow. Red ncha w r- * / ch, ch, coochg
129 „ / Wfj * (CH30)2S02 gelbst. Rot 129 "/ Wfj * (CH30) 2S02 yellow. red
NCHj NCHj
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Beis By S
130 130
131 131
132 132
133 133
134 134
135 135
136 136
137 137
138 138
139 139
39 39
40 40
Diazokomponente Kupplungskomponente Quaternierungsmittel Diazo component coupling component quaternizing agent
$ ò $ ò
w 'CltCH.SOiCH, w 'CltCH.SOiCH,
w w
^ch,chso1-0 ^ ch, chso1-0
(ch30)2s02 (ch30) 2s02
(ch30)2s02 (ch30) 2s02
^ /C^CHaCl ck ~ (ch30)2s02 ^ / C ^ CHaCl ck ~ (ch30) 2s02
xCHj CHjj Cî^ Cl xCHj CHjj Cî ^ Cl
I I.
s, s,
(ch30)2s02 (ch30) 2s02
/_. /ch- ch- ocochg n vj-, w (ch,0)2s02 / _. / ch- ch- ocochg n vj-, w (ch, 0) 2s02
N CH® "W N CH® "W
/—v ^HgCHaOCONCCHs )a / —V ^ HgCHaOCONCCHs) a
(ch30)2s02 (ch30) 2s02
^ /chg chg cn ^ / chg chg cn
(/ \Vn ^ (/ \ Vn ^
/chj chj cn (' y-n / chj chj cn ('y-n
NCHa «O NCHa «O
N02 N02
_ /(CH, ), N(C, H, ), ,0% CI4 OCONH-^^ _ / (CH,), N (C, H,),, 0% CI4 OCONH - ^^
(ch30)2s02 (ch30) 2s02
(ch30)2s02 (ch30) 2s02
(ch30)2s02 (ch30) 2s02
o O
(ch30)2s02 (ch30) 2s02
6469/73 6469/73
Beis] By S]
140 140
141 141
142 142
143 143
144 144
145 145
146 146
147 147
148 148
41 42 41 42
Diazokomponente Kupplungskomponente Quaternierungsmittel Diazo component coupling component quaternizing agent
H.C^CHa H.C ^ CHa
(^VNH-CEj CHg (^ VNH-CEj CHg
ô O
Cl Cl
/TTv / ca hb / TTv / ca hb
CHj CHj
CH, ^ CH, ^
<f>n nch,CH,.0> <f> n nch, CH, .0>
/r\ /ch2 "^3 / r \ / ch2 "^ 3
^CH^CN ^ CH ^ CN
nch2cha-^3 nch2cha- ^ 3
?=j sch2 -<f n) ? = j sch2 - <f n)
CH, CH,
<t>/c^cxn k; ^-O <t> / c ^ cxn k; ^ -O
>=^"ch,-fS > = ^ "ch, -fS
r.v. \=/ r.v. \ = /
(ch30)2s02 (ch30) 2s02
(ch3o)2so2 (ch3o) 2so2
chjci chjci
CH3C1 CH3C1
ch,c1 ch, c1
£>cu -o mhcochg ^=s £> cu -o mhcochg ^ = s
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Beispiel Diazokomponente Kupplungskomponente Ouaternierungsmittel Farbton auf Example Diazo component Coupling component Ouaternierungsmittel color
Polyacrylnitril h«c1 Polyacrylonitrile h «c1
q-»c^cxc"h5 ' ò ch° q- »c ^ cxc" h5 'ò ch °
157 157
^ xchjchgnhcho ^ xchjchgnhcho
150 „ V NVN /r-^ „ Rot 150 "V NVN / r- ^" Red
W -ch, O W -ch, O
Cfij x=/ Cfij x = /
151 „ (f ^VN r—v •• Rot 151 „(f ^ VN r — v •• red
✓ chach2sq,ch9 ✓ chach2sq, ch9
pvo chg w pvo chg w
/cha chj nhsoj c2 he / cha chj nhsoj c2 he
152 „ \—f"K /7~^< » Rot pvo 152 "\ —f" K / 7 ~ ^ <»red pvo
^cha chjj nhconhchg ^ cha chjj nhconhchg
153 K_7'Nv /T5V " Rot pvo ch, x=/ 153 K_7'Nv / T5V "Red pvo ch, x = /
/t^. /ch, ch nhco-0-ck, / t ^. / ch, ch nhco-0-ck,
w""ch, -0 w "" ch, -0
rw \=ZJ rw \ = ZJ
154 <y_ V"N /rr\ — » Rot ch, 154 <y_ V "N / rr \ -» red ch,
/cha ch^ ococji h8 / cha ch ^ ococji h8
155 „ (' x>n /--\ „ Rot irsch°^> 155 "('x> n / - \" red irish ° ^>
oc hg oc ed
/ch. ch. och- ch. / ch. ch. och.
156 „ (' X>N ^ " Rot ps*-0 156 "('X> N ^" Red ps * -0
ru \sn/ ru \ sn /
Vi.* Vi. *
,0h, cha ocoocife Rot ce , 0h, cha ocoocife red ce
/r^v /chjch, och5 / r ^ v / chjch, och5
p<«o p <«o
158 p/-' (CH30)2S02 Rot dht 158 p / - '(CH30) 2S02 red dht
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159 159
160 160
161 161
162 162
163 163
164 164
165 165
166 166
167 167
168 168
45 45
46 46
Diazokomponente Kupplungskomponente Quaternierungsmittel Farbton auf Diazo component coupling component quaternizing agent color
Polyacrylnitril Polyacrylonitrile
•ç-"* çx*-o • ç - "* çx * -o
ô O
_ ,CH, CHj COOC, H, _, CH, CHj COOC, H,
chg y=f chg y = f
CH, CH,
(ch30)2s02 Rot (ch30) 2s02 red
(ch30)2s02 Rot (ch30) 2s02 red
(ch30)2s02 Rot (ch30) 2s02 red
(ch30)2s02 Rot (ch30) 2s02 red
(ch30)2s02 Rot ch»"0 (ch30) 2s02 red ch »" 0
/CHjCHjCl / CHjCHjCl
CH, w CH, w
_ ,Cf4CH,CH,Br p v c hj x=/ _, Cf4CH, CH, Br p v c hj x = /
^ ^HaC^OCOCHa-o ^ ^ HaC ^ OCOCHa-o
>=/^chà (ch3o)2so2 Rot ch, > = / ^ chà (ch3o) 2so2 red ch,
^ /ÎHaCHa 0C0N(CI^ )2 ^ / ÎHaCHa 0C0N (CI ^) 2
\-/■? /t*\ (ch30)2s02 Rot ch," ch* \ - / ■? / t * \ (ch30) 2s02 red ch, "ch *
/CH, CHg 0$0t N(Cî% )2 / CH, CHg 0 $ 0t N (Cî%) 2
s«' ^ch, (ch30)2s02 Rot ch, 1 s «'^ ch, (ch30) 2s02 red ch, 1
je-* /CHaCHgCN chg w each- * / CHaCHgCN chg w
(ch30)2s02 Rot j-/(CHg )a N(CI^ ), (ch30) 2s02 red j - / (CHg) a N (CI ^),
pv-o pv-o
CHg W CHg W
(ch30)2s02 Rot (ch30) 2s02 red
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170 170
171 171
172 172
173 173
174 174
175 175
176 176
177 177
178 178
47 47
48 48
Diazokomponente Kupplungskomponente Quaternierungsmittel h" v/"5 /T^. 'CH* CB» °conh-0-CI Diazo component coupling component quaternizing agent h "v /" 5 / T ^. 'CH * CB »° conh-0-CI
ò cha ò cha
}scjÖ~ s(¥ch ch,, } scjÖ ~ s (¥ ch ch ,,
q-nhch, -0 q-no, -0
ochs ox
^J^-NHCHg CH^ -^2^ ^ J ^ -NHCHg CH ^ - ^ 2 ^
(CH30)2S02 (CH30) 2S02
^^-nhcha cha cha ^^ - nhcha cha cha
^J^-NH-CHgCHa och3 /© ^ J ^ -NH-CHgCHa och3 / ©
ch, ch,
P"Wh,.0 P "Wh, .0
chg x—7 chg x-7
y«-ä /cha cha cn cha w oc hg y «-ä / cha cha cn cha w oc hg
'cf he 'cf he
^ schacha^o cha x=i/ ^ schacha ^ o cha x = i /
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h2c1 h2c1
49 49
50 50
Beispiel Diazokomponente Kupplungskomponente Example diazo component coupling component
Quaternierungsmittel Quaternizing agent
Farbton auf Polyacrylnitril Color on polyacrylonitrile
179 179
hsc. cha hsc. cha
Ns3-NK, Ns3-NK,
180 180
ochj ochj
✓ c.h, ✓ c.h,
0"%h,ck,-0 0 "% h, ck, -0
oc ho w oc. h, oc ho w oc. H,
0,cths nhcocho n—' 0, cths nhcocho n— '
Q-oh2oi blaust. Rot blaust. Rot Q-oh2oi bluish. Red bluish. red
181 181
H*c. H * c.
182 182
w 8 w 8
ó O
183 183
184 184
P/c!hb P / c! Hb
"VCH,0 "VCH, 0
ci ci
^-nhch-q cha ^ -nhch-q cha
^J^-NHCHg cl ^ J ^ -NHCHg cl
(ch30)2s02 (ch30) 2s02
(ch3o)2so2 (ch3o) 2so2
(ch30)2s02 (ch30) 2s02
Rot rotst. Orange Red red orange
Rot red
Rot red
185 185
186 186
oc hg jß-§. scih oc hg jß-§. scih
(ch30)2s02 (ch30) 2s02
(ch30)2s02 (ch30) 2s02
Rot gelbst. Rot Red yellow. red
187 187
oc** oc **
CH*-© CH * - ©
(ch30)2s02 (ch30) 2s02
gelbst. Rot yellow. red
188 188
/t^\ /c3h» / t ^ \ / c3h »
(ch30)2s02 (ch30) 2s02
gelbst. Rot yellow. red
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190 190
191 191
192 192
193 193
194 194
195 195
196 196
197 197
198 198
51 51
52 52
Diazokomponente Kupplungskomponente Quaternierungsmittel h»c c,h, Diazo component coupling component quaternizing agent h »c c, h,
oco ok
ô O
sch, -^3 /h) sh, - ^ 3 / h)
(ko« (ko «
^c-ch ^ c-ch
(CH30)2S02 (CH30) 2S02
(CH30)2S02 (CH30) 2S02
(ch3o)2so2 (ch3o) 2so2
(CH30)2S02 (CH30) 2S02
(CH30)2S02 (CH30) 2S02
(CH3o)2so2 (CH3o) 2so2
/■ *\ /Cg Ha ov-© / ■ * \ / Cg Ha ov- ©
no, no,
^^-nhchj ch, -<^> h ^^ - nhchj ch, - <^> h
^^-nhcha chjj ^^ - nhcha chjj
^Vc*-© ^ Vc * - ©
V N>N jt-tv (CH30)2S02 V N> N jt-tv (CH30) 2S02
vf *<*.& vf * <*. &
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200 200
201 201
202 202
203 203
204 204
205 205
206 206
207 207
208 208
53 53
54 54
Diazokomponente Kupplungskomponente Quaternierungsmittel h»c ca h3 Diazo component coupling component quaternizing agent h »c ca h3
^ p-ncq o ^ p-ncq o
f\ h/c*h' >=/ N5H-0 f \ h / c * h '> = / N5H-0
oc ha >=/ oc ha> = /
NHC0CHr X=/ NHC0CHr X = /
OCHj OCHj
A Hs A ms
OC H. OC H.
// v y // v y
3 3rd
C« H C «H
a "b a "b
NHC0Ca .i„ NHC0Ca .i "
"CH, "(3 '«H, W "CH," (3 '«H, W
A Hi A Hi
CH3 CH3
j7~\ A H» j7 ~ \ A H »
pv-o pv-o
0c0 0c0
»co »Co
(ch30)2s02 (ch30) 2s02
(Ch3o)2so2 (Ch3o) 2so2
/—-rv /C. H» / —- rv / C. H"
Z' ^VlT y t (C2H50)2S02 Z '^ VlT y t (C2H50) 2S02
(C2h5o)2so2 (C2h5o) 2so2
OCH-// \\ /C2H8 OCH - // \\ / C2H8
y=/ X Cî^ jT^ (C2HS0)2S02 y = / X Cî ^ jT ^ (C2HS0) 2S02
OC Ho n (c2h50)2s02 OC Ho n (c2h50) 2s02
(c2hs0)2s02 (c2hs0) 2s02
c,H,Br c, H, Br
C2H5Br C2H5Br
/—V CYU CH. N; / —V CYU CH. N;
<f3*N /T^ CH3 C2H,Br <f3 * N / T ^ CH3 C2H, Br
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Beispiel Diazokomponente Kupplungskomponente Quaternierungsmittel Farbton auf Example diazo component coupling component quaternizing agent color
Polyacrylnitril Polyacrylonitrile
— -
v ' „ch, ch, nhcoch, v '„ch, ch, nhcoch,
209 NCm^-NH. V__7-N C2H5Br gelbst. Rot 209 NCm ^ -NH. V__7-N C2H5Br yellow. red
210 210
ô 0 ô 0
<x <x
ÇH ÇH
ch, ch, nhso, C2H5Br gelbst. Rot cha-ö ch, ch, nhso, C2H5Br yellow. Red cha-ö
NH, NH,
/—ry /ch, ch, nhco / —Ry / ch, ch, nhco
211,, (/ ^Vn /r-\ C2H5Br gelbst. Rot 211 ,, (/ ^ Vn / r- \ C2H5Br yellow. Red
W \r r-* /ch, ch, nhc0-(q> We \ r- * / ch, ch, nhc0- (q>
212 W^CH. jP A C2H5Br gelbst. Rot 212 W ^ CH. jP A C2H5Br yellow. red
^ w ^ w
^ /CH,CH,NHC0-/^-a ^ / CH, CH, NHC0 - / ^ - a
2I3 - <^-N ^ — C2H5Br gelbst. Rot 2I3 - <^ - N ^ - C2H5Br yellow. red
/t-a ,ch,ch,0c0chb / t-a, ch, ch, 0c0chb
214 (f y-n (CH30)2S02 gelbst. Rot 214 (f y-n (CH30) 2S02 yellow. Red
\=y \ = y
r.—r». /ch, ch, och, ch, oh r. — r ». / ch, ch, och, ch, oh
215 „ <' N>N j v (CH30)2S02 gelbst. Rot 215 "<'N> N j v (CH30) 2S02 yellow. red
\_y \ _y
,ch,ch, ocoochj , ch, ch, ocoochj
/71\ A _ _ / 71 \ A _ _
216 V VN /7*"7\ (CH30)2S02 gelbst. Rot 216 V VN / 7 * "7 \ (CH30) 2S02 yellow. Red
^ /CH,C^0C^, ^ / CH, C ^ 0C ^,
217 „ \_/ N /7~^ (CH30)2S02 gelbst. Rot ch2"0 217 „\ _ / N / 7 ~ ^ (CH30) 2S02 yellow. Red ch2 "0
SCH, SCH,
218 ( /-n v x ' (CH30)2S02 gelbst. Rot 218 (/ -n v x '(CH30) 2S02 yellow. Red
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Diazokomponente Kupplungskomponente Quaternierungsmittel Farbton auf Diazo component coupling component quaternizing agent color
Polyacrylnitril Polyacrylonitrile
HBC C,HB HBC C, HB
ò w ò w
(CH30)2S02 gelbst. Rot (CH30) 2S02 yellow. red
CH2 SO^ CU CH2 SO ^ CU
ck, ^ ck, ^
(CH30)2S02 gelbst. Rot (CH30) 2S02 yellow. red
A^IIa OITte UU« A ^ IIa OITte UU «
^ /CH.CH.C. ^ /CH.CH.C.
(/ \Vn —, (/ \ Vn -,
s CH, s CH,
^ /CH, CH, CHj Cl ^ / CH, CH, CHj Cl
(CH30)2S02 gelbst. Rot (CH30) 2S02 yellow. red
(CH30)2S02 gelbst. Rot (CH30) 2S02 yellow. red
(CH30)2S02 gelbst. Rot (CH30) 2S02 yellow. red
/CH,CH, OCOCH, -^3 / CH, CH, OCOCH, - ^ 3
V \>N ,—v —'' (CH30)2S02 gelbst. Rot V \> N, —v - '' (CH30) 2S02 yellow. red
VCH, VCH,
,CH, CH, OCON(CI^ ), , CH, CH, OCON (CI ^),
2 2nd
^■o ^ ■ o
(CH30)2S02 gelbst. Rot (CH30) 2S02 yellow. red
/wh SCH, -^^-CJ / wh SCH, - ^^ - CJ
WNck>^ WNck> ^
(CH30)2S02 gelbst. Rot (CH30) 2S02 yellow. red
(CH30)2S02 gelbst. Rot (CH30) 2S02 yellow. red
NOy NOy
,(CH,)SN(C,H,), SCH, -^3 , (CH,) SN (C, H,), SCH, - ^ 3
(CH30)2S02 gelbst. Rot (CH30) 2S02 yellow. red
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229 229
230 230
231 231
232 232
233 233
234 234
235 235
236 236
237 237
238 238
59 59
60 60
Diazokomponente Kupplungskomponente Quaternierungsmittel h.c ç,h, Diazo component coupling component quaternizing agent h.c ç, h,
W* ' /chtch«oconh-^> W * '/ chtch «oconh - ^>
ò O
(j^-NH-CH, Cl^ (j ^ -NH-CH, Cl ^
Cl ■ c, h fv 18 ^ Cl ■ c, h fv 18 ^
v=^ NCH, CHg "\y cha x=/ v = ^ NCH, CHg "\ y cha x = /
__ xd a» _ __ xd a »_
^ck,-© ^ ck, - ©
/CH.CI^N^U \=/'^CHjCH, /CH.CI^N^U \ = / '^ CHjCH,
mhcochg mhcochg
V=/ NîHj NN| V = / NîHj NN |
ch,, ch ,,
„ /CH.CH.CN // Wm' "/CH.CH.CN // Wm '
p"- p "-
=/ ^ch,^ ,ch,ch,0h pvo = / ^ ch, ^, ch, ch, 0h pvo
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(CH30)2S02 (CH30) 2S02
(CH30)2S02 (CH30) 2S02
(CH30)2S02 (CH30) 2S02
CH3C1 CH3C1
CH,C1 CH, C1
CH3C1 CH3C1
pcch. <□> "tO**™* pcch. <□> "tO ** ™ *
61 61
62 62
Beispiel Diazokomponente Kupplungskomponente Quaternierungsmittel Farbton auf Example diazo component coupling component quaternizing agent color
Polyacrylnitril h^c ca ! Polyacrylonitrile h ^ c ca!
Vi /T^ ^CH,CH,N(CtH,), Vi / T ^ ^ CH, CH, N (CtH,),
n^nh, Bf-(j-3¥c'b r°' n ^ nh, Bf- (j-3 ¥ c'b r ° '
ÒCHj /""\ '' ÒCHj / "" \ ''
240 „ / Ns. /T^\ „ Rot 240 "/ Ns. / T ^ \" Red
CHj, CHj,
247 247
CHg CHg NHCHO CHg CHg NHCHO
yCJ^CHjSOjCHa pv <^> yCJ ^ CHjSOjCHa pv <^>
241 „ Rot 241 "Red
CHg CHg
CH2 NHSQ, C, Hg CH2 NHSQ, C, ed
242 " 7"H i5-T\ Rot ch, 242 "7" H i5-T \ Rot ch,
>=•/ ^ch,/^ > = • / ^ ch, / ^
f!H_ *=/ f! H_ * = /
P.CHa CHa NHCONHCH. N /—V „ Rot P.CHa CHa NHCONHCH. N / —V "Red
^CHjj CHj NHC0-^>-CH3 ^ CHjj CHj NHC0 - ^> - CH3
244 „ (' »>N r—\ » Rot 244 „('»> N r— \ »red
/r-Ä /wijj V/fia «r p-^o ch3 \=/ / r-Ä / wijj V / fia «r p- ^ o ch3 \ = /
^_n/CH2 CHa 0C0Ca H8 ^ _n / CH2 CHa 0C0Ca H8
245 " 245 "
CHa X=/ CHa X = /
OCH, OCH,
-Ä /CH, CHa OCHj CH. -Ä / CH, CHa OCHj CH.
246 (' W „ R« 246 ('W "R"
cp cp
P^HaCHgOCOOCI^, P ^ HaCHgOCOOCI ^,
^cha -f3"c1 ^ cha -f3 "c1
ck, w a/ ^ a" ck, w a / ^ a "
Rot red
'CHa CHa OCHg 'CHa CHa OCHg
248 » <' /-ry. (CH30)2S02 Rot 248 »<'/ -ry. (CH30) 2S02 red
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Beispiel Diazokomponente Kupplungskomponente Ouaternierungsmittel Farbton auf Example Diazo component Coupling component Ouaternierungsmittel color
Polyacrylnitril Polyacrylonitrile
^ .ch.ch.ohq ^ .ch.ch.ohq
249 NxKT>NHa (' N>N ' (CH30)2S02 Rot x y^-o 249 NxKT> NHa ('N> N' (CH30) 2S02 red x y ^ -o
/CHg Cf^ COOCg Hg / CHg Cf ^ COOCg Hg
250 „ (f nvn /t-7v (CH30)2S02 Rot 250 "(f nvn / t-7v (CH30) 2S02 red
/7-a /ungwngww chj / 7-a / ungwngww chj
/CHg CHg SO, / CHg CHg SO,
251 „ (/ \S-N J v (CH30)2S02 Rot y*™-® 251 "(/ \ S-N J v (CH30) 2S02 Red y * ™ -®
,CHg CHg Cl , CHg CHg Cl
252 „ (' 7-N (CH3o)2so2 Rot 252 „('7-N (CH3o) 2so2 red
/7"tv /v-xtg n-rig vj. / 7 "tv / v-xtg n-rig vj.
P^o ch, P ^ o ch,
/CHg CHg CHg Br / CHg CHg CHg Br
=7' = 7 '
pu pu
253 „ KT1* " (CH30)2S2 Rot 253 "KT1 *" (CH30) 2S2 red
>=/ vCHg // y-Br -u \s/ > = / vCHg // y-Br -u \ s /
„ ^c^ococh,^) >=/ "^ C ^ ococh, ^)> = /
nu w/ nu w /
254 „ >n /7~\ (CH30)2S02 Rot chj 254 „> n / 7 ~ \ (CH30) 2S02 red chj
^ .CHgCHgOCONCCHs )2 ^ .CHgCHgOCONCCHs) 2
255 // \>N /r-TV (CH30)2S02 Rot 255 // \> N / r-TV (CH30) 2S02 red
W W
chs w chs w
.chgchgosogncchs )a .chgchgosogncchs) a
256 „ W ^CHg (CH3°)2S°2 ROt ch3 2 256 "W ^ CHg (CH3 °) 2S ° 2 ROt ch3 2
^cf^chgcn ^ cf ^ chgcn
257 „ (' >N yj-A (CH30)2S02 Rot x rig ^ 257 „('> N yj-A (CH30) 2S02 red x rig ^
y/^chg oci chs w y / ^ chg oci chs w
^ /(ch|)5n(ch)t ^ / (ch |) 5n (ch) t
Pv<o> Pv <o>
258 S=>N - (CH30)2S02 Rot 258 S => N - (CH30) 2S02 red
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260 260
261 261
262 262
263 263
264 264
265 265
266 266
267 267
268 268
65 65
66 66
Diazokomponente Kupplungskomponente Quaternierungsmittel Diazo component coupling component quaternizing agent
8 8 ,CHg CHg 0C0NH-^3"C1 8 8, CHg CHg 0C0NH- ^ 3 "C1
/7~^ (CH30)2S02 / 7 ~ ^ (CH30) 2S02
à '"-<2 à '"- <2
<^-NHCHg <^ - NHCHg
CH, CH,
^3-NHCHg CH2 ^ 3-NHCHg CH2
CH, CH,
^^-NH-CHg CHg OCH, ^^ - NH-CHg CHg OCH,
z-x/è) z-x / è)
P"vc^-0 P "vc ^ -0
fi V. N fi V. N
n-ch* c> n-ch * c>
CHg CHg-^> CHg CHg - ^>
CI^ CI ^
/CHg CHg CN / CHg CHg CN
S^chgc^/} S ^ chgc ^ /}
CH, CH,
0CHs 0CHs
,C2H8 , C2H8
^=^"^CHg CHg-<^3 ^ = ^ "^ CHg CHg - <^ 3
*W_ * W_
CH, CH,
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270 270
271 271
272 272
273 273
274 274
275 275
276 276
277 277
278 278
67 67
68 68
Diazokomponente Kupplungskomponente Ouaternierungsmittel hb OCHs Diazo component coupling component ouating agent hb OCHs
0<cCcH, -© 0CH^C1 0 <cCcH, - © 0CH ^ C1
OC Ha oc, hb OC Ha oc, hb
0/0« H5 0/0 «H5
NHCOCH, NHCOCH,
/ca h3 / ca h3
PVCH.0 PVCH.0
ci — ci -
Qjp* Qjp *
0-nhch, 0-nhch,
Ò O
^^-NHCHg chg ^^ - NHCHg chg
^^-NHCH, ^^ - NHCH,
ci ci
^-NHCH, ^ -NHCH,
OC Ha OC Ha
0Nsch,^ 0Nsch, ^
OCo OCo
(ch30)2s02 (ch30) 2s02
(ch,0)2s02 (ch, 0) 2s02
(ch30)2s02 (ch30) 2s02
(CH30)2S02 (CH30) 2S02
(ch30)2s02 (ch30) 2s02
oCJ'-o (chio,ìso1 oCJ'-o (chio, ìso1
(ch30)2s02 (ch30) 2s02
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280 280
281 281
282 282
283 283
284 284
285 285
286 286
287 287
288 288
69 69
70 70
Diazokomponente Diazo component
Kupplungskomponente Coupling component
Quaternierungsmittel Quaternizing agent
Farbton auf Polyacrylnitril Color on polyacrylonitrile
% %
Ò O
OV -0 OV -0
oc* -<q oc * - <q
XE) XE)
oç<> oç <>
(ch30)2s02 (ch30) 2s02
(ch3o)2ch2 (ch3o) 2ch2
(ch30)2s02 (ch30) 2s02
(ch3o)2s2 (ch3o) 2s2
Rot gelbst. Rot Red yellow. red
Rot red
Rot red
Of* Of *
"chg "chg
(ch30)2s02 (ch30) 2s02
Rot y \ /c* h. Red y / c * h.
no, no,
(ch30)2s02 (ch30) 2s02
^-nhcha ch, t^c-^)-3^0c^ ^ -nhcha ch, t ^ c - ^) - 3 ^ 0c ^
Rot rotst. Orange Red red orange
^j^-nhch, ch,~£^ ^ j ^ -nhch, ch, ~ £ ^
c* c *
rotst. Orange red orange
/7-!\ 'c2h5 / 7 -! \ 'C2h5
Rot red
.ch3 .ch3
(ch30)2s02 (ch30) 2s02
Rot red
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290 290
291 291
292 292
293 293
294 294
295 295
296 296
297 297
298 298
71 71
72 72
Diazokomponente Diazo component
Kupplungskomponente Coupling component
Quaternierungsmittel Quaternizing agent
'hb >-nh, 'hb> -nh,
ì1 ì1
y - y -
cl cl
S=s "•ch.-f]) S = s "• ch.-f])
OCHj x=y OCHj x = y
(CH30)2S02 (CH30) 2S02
(CH30)2S02 (CH30) 2S02
r. a /ca h# r. a / ca h #
v=^" ncn nhcochj n=/ .och, v = ^ "ncn nhcochj n = / .och,
g G
OCH« ^ ✓pt h, OCH «^ ✓pt h,
w sch./^ w sch./^
ochj \=/ ochj \ = /
och. och
^ ah» ^ ah »
çk* çk *
nhcocj h5 nhcocj h5
/7~\ ah» / 7 ~ \ ah »
oco ok
(C2HS0)2S02 (C2HS0) 2S02
(c2h5o)2so2 (c2h5o) 2so2
(C2H50)2S02 (C2H50) 2S02
(C2H50)2S02 (C2H50) 2S02
(C2H50)2S02 (C2H50) 2S02
C2H,Br C2H, Br
^ ^chj ch, oh o^ch,0 ^ ^ chj ch, oh o ^ ch, 0
o< o <
/cht0^r / cht0 ^ r
/chj / chj
cha cha
C2H,Br C2H, Br
C,H,Br C, H, Br
6469/73 6469/73
73 73
74 74
Beispiel Diazokomponente Kupplungskomponente Example diazo component coupling component
299 299
300 300
301 301
Ou* Ou *
Ò O
Or Or
/chg ch,nhc0ch* / chg ch, nhc0ch *
CHa"ö CHa "ö
Ç«, Ç «,
ch, ch, nhso, ch, ch, nhso,
w .cht-0 w .cht-0
nh, ch, ch, nhco nh, ch, ch, nhco
Quaternierungsmittel Quaternizing agent
C2H5Br C2H5Br
C2HsBr C2HsBr
C2H5Br C2H5Br
Farbton auf Polyacrylnitril Color on polyacrylonitrile
Rot red
Rot red
Rot red
302 302
303 303
.chgchgnhco- .chgchgnhco-
X VN /—> x=/ X VN / -> x = /
C2H5Br ch, cil nhcoh^^vci k rn /-tv w c2h: C2H5Br ch, cil nhcoh ^^ vci k rn / -tv w c2h:
sch, sh
Br Br
Rot red
Rot red
304 304
\=y v ch,ch,0c0ch^ \ = y v ch, ch, 0c0ch ^
c^-o c ^ -o
(CH3o)2so2 (CH3o) 2so2
Rot red
305 305
306 306
<&( <& (
/ïh, ch, och, ch, oh / ïh, ch, och, ch, oh
CHg CHg OCOOCHb ch«-ö CHg CHg OCOOCHb ch «-ö
(CH30)2S02 (CH30) 2S02
(CH30)2S02 (CH30) 2S02
Rot red
Rot red
307 307
308 308
£>* £> *
/CH,C^|0CH / CH, C ^ | 0CH
nCH,hq> nCH, hq>
(CH30)2S02 (CH30) 2S02
(CH3o)2so2 (CH3o) 2so2
Rot red
Rot red
6469/73 6469/73
75 75
76 76
Beispiel Diazokomponente Kupplungskomponente Ouaternierungsmittel Farbton auf Example Diazo component Coupling component Ouaternierungsmittel color
Polyacrylnitril Polyacrylonitrile
/CHg CHg COOCHfe / CHg CHg COOCHfe
309 / V (CH30)2S02 Rot 309 / V (CH30) 2S02 red
QcHb QcHb
«g-«* QCTi" "G -" * QCTi "
o O
—1 /C^C^S^CHi, —1 / C ^ C ^ S ^ CHi,
310 .. (CH.OhSO, R.« 310 .. (CH.OhSO, R. «
CHjCHSCi CHjCHSCi
311 S y-N /—rv (CH30)2S02 Rot 311 S y-N / -rv (CH30) 2S02 red
^ /CHg CHg Cl ^ / CHg CHg Cl
312 „ e X>N V (CH30)2S02 Rot wvch*-0 312 „e X> N V (CH30) 2S02 red wvch * -0
/TTV /'CHg CHg CHg Cl / TTV / 'CHg CHg CHg Cl
313 (/ \>N r-jv (CH30)2S02 Rot w CHg r— ,CHgCHgOCOCHg n z-* w 313 (/ \> N r-jv (CH30) 2S02 red w CHg r—, CHgCHgOCOCHg n z- * w
'CHa -^) 'CHa - ^)
314 C /~N /-TV (CH30)2S02 Rot 314 C / ~ N / -TV (CH30) 2S02 red
,CHg CHj 0C0N(CHg )g 315 .. C/^ch,^ (CH.OhSO, Ro. , CHg CHj 0C0N (CHg) g 315 .. C / ^ ch, ^ (CH.OhSO, Ro.
. /CHg CHg CN . / CHg CHg CN
316 il \>N r-^ (CH30)2S02 Rot 316 il \> N r- ^ (CH30) 2S02 red
\=y Vw. -rf/VS \ = y Vw. -rf / VS
cha "c^"c1 cha "c ^" c1
~ .CHgCHgCN ~ .CHgCHgCN
317 'S y*N (CH30)2S02 Rot 317 'S y * N (CH30) 2S02 red
"ch2 \Jy "ch2 \ Jy
NOg yÇ-rv /(CHg )3 N(Ca H# )g NOg yÇ-rv / (CHg) 3 N (Ca H #) g
318 & \>N j (CH30)2S02 Rot 318 & \> N j (CH30) 2S02 red
^ CHg ^ CHg
6469/73 6469/73
Beis By S
319 319
320 320
321 321
322 322
323 323
324 324
325 325
326 326
327 327
328 328
77 77
78 78
Diazokomponente Kupplungskomponente Quaternierungsmittel Diazo component coupling component quaternizing agent
^ eCo"0 ^ eCo "0
ò O
Cl Cl
/r^\ /^2n8 / r ^ \ / ^ 2n8
ch| ch |
chg x=/ chg x = /
/~\® / ~ \ ®
/r^\ /ch2 -^3 / r ^ \ / ch2 - ^ 3
ch, chj; ch, chj;
^CHaCHaCN ^ CHaCHaCN
x chg ck2 x chg ck2
CK... _ w CK ... _ w
/CH.CH^CN / ch, ch2 oh /CH.CH^CN / ch, ch2 oh
Pv-o Pv-o
(ch30)2s02 (ch30) 2s02
(ch30)2s02 (ch30) 2s02
(ch30)2s02 (ch30) 2s02
chjci ch3c1 chjci ch3c1
ch,ci ch, ci
£>€£* o ^O00"- £> € £ * o ^ O00 "-
nticochj y/ v nticochj y / v
^chj n ^ chj n
6469/73 6469/73
79 79
80 80
Beispiel Diazokomponente Kupplungskomponente Quaternierungsmittel Farbton auf Example diazo component coupling component quaternizing agent color
Polyacrylnitril gl,01 Polyacrylonitrile gl, 01
Ò O
/-tv /CHtCHtN(CaH8 )a ^ / -tv / CHtCHtN (CaH8) a ^
329 N^-NH, Hp^aJOOH, blaust. Ro, 329 N ^ -NH, Hp ^ aJOOH, bluish. Ro,
chj *=/ chj * = /
CHgCHgNHCHO CHgCHgNHCHO
330 „ V ^"1 >5""^. " blaust. Rot yç-rv ' v"a *«« "" 330 "V ^" 1> 5 "" ^. "Bluish. Red yç-rv 'v "a *« "" "
ÇK*C ÇK * C
-m \=l/ -m \ = l /
chg ci^c^sojchg chg ci ^ c ^ sojchg
331 ,, (' /r""vV „ blaust. Rot 331 ,, ('/ r "" vV „bluish red
CHg W CHg W
xCHjj CHg NHSO, Ct Hg xCHjj CHg NHSO, Ct Hg
332 „ (' X^"N /TV ,, blaust. Rot 332 "('X ^" N / TV ,, bluish red
F<:- o F <: - o
CH2 CHs NHCONHCHg CH2 CHs NHCONHCHg
333 „ C *>N /7TV " blaust. Rot 333 "C *> N / 7TV" bluish. Red
^«2 ^ «n ^ «2 ^« n
Pvo Pvo
CHg X-y CHg X-y
^ ^hachjnhco/jv0^ ^ ^ hachjnhco / jv0 ^
334 <' >N /—v blaust. Rot 334 <'> N / - v bluish. red
,CH2 CHa ococa Hg , CH2 CHa ococa ed
335 „ U XVN' /—V « blaust. Rot 335 “U XVN '/ —V” bluish. red
/7~~\ /^n«v,n,w / 7 ~~ \ / ^ n «v, n, w
P^C P ^ C
CHg och. CHg och.
XHj CHg OCH, C^ XHj CHg OCH, C ^
336 „ (f NVN .. blaust. Rot 336 "(f NVN .. bluish red
/T\ / T \
.CHg CH, OCOOCHg .CHg CH, OCOOCHg
337 „ (f *\.N __ „ blaust. Rot 337 "(f * \. N __" bluish. Red
>/ ^h, />c1 CHS > / ^ h, /> c1 CHS
• CHg CHz OCHg • CHg CHz OCHg
338 „ (' >n /rvv CH2=CH-CH2Br blaust. Rot 338 „('> n / rvv CH2 = CH-CH2Br bluish red
/tw * 2-7' / tw * 2-7 '
ì^ch,/} ì ^ ch, /}
ck, w ck, w
6469/73 6469/73
Beisi Beisi
339 339
340 340
341 341
342 342
343 343
344 344
345 345
346 346
347 347
348 348
81 81
82 82
Diazokomponente Kupplungskomponente Quaternierungsmittel Diazo component coupling component quaternizing agent
Qch, Qch,
ò O
^./ch.c^o-Q ^. / ch.c ^ o-Q
/ (/ NVn' ~ CH2=CH-CH2Br / (/ NVn '~ CH2 = CH-CH2Br
"^o chg w "^ o chg w
~ ^chgchgcoocghg ~ ^ chgchgcoocghg
Pvo Pvo
CH2=CH-CH2Br CH2 = CH-CH2Br
✓CHa CHt SP» "^3 ✓CHa CHt SP »" ^ 3
Pvo Pvo
CH2=CH-CH2Br chg r-*. /CH,CH,C1 CH2 = CH-CH2Br chg r- *. / CH, CH, C1
Può Può
CH, W CH, W
/Cl^CH, CH, Br / Cl ^ CH, CH, Br
7' 7 '
CHg CHg
CH2=CH-CH2Br CH2 = CH-CH2Br
™ /CH, CH, CH, Bx ™ / CH, CH, CH, Bx
ÇK* ^>br ÇK * ^> br
:hj \=/ : hj \ = /
,ch, c* 0c0ch(o , ch, c * 0c0ch (o
CHg w CHg w
CH2=CH-CH2Br CH2 = CH-CH2Br
CH2=CH-CH2Br CH2 = CH-CH2Br
^ ^hgchaoconcci^ ), ^ ^ hgchaoconcci ^),
w "ch, -fs chs w "ch, -fs chs
,0h, ch, oso, n(cffe )b , 0h, ch, oso, n (cffe) b
CH2=CH-CH2Br CH2 = CH-CH2Br
/r\ / r \
P^o P ^ o
PCS PCS
CH2=CH-CH2Br ci CH2 = CH-CH2Br ci
/r-*. /(ch, )an(chg ), / r- *. / (ch,) an (chg),
7 NVn >ì-rv 7 NVn> ì-rv
/r~\ 's p--,ö / r ~ \ 's p -, ö
CH2=CH-CH2Br y -ch, <j) CH2 = CH-CH2Br y -ch, <j)
CHg CHg
6469/73 6469/73
Beis By S
349 349
350 350
351 351
352 352
353 353
354 354
355 355
356 356
357 357
358 358
83 84 83 84
Diazokomponente Kupplungskomponente Ouaternierungsmittel Diazo component Coupling component Ouaternizing agent
^3-NHCH, CHj CH, ^ 3-NHCH, CHj CH,
^3*nh-chg ch^ ^ 3 * nh-chg ch ^
och8 och8
^ ch, ch ^ ch, ch
CHg X=/ CHg X = /
ÇXllScï O°20°2h5 ÇXllScï O ° 20 ° 2h5
ch, ch,
^ /CHj CHj CN ^ / CHj CHj CN
CHa x-/ CHa x- /
OCHa fl/"2"8 OCHa fl / "2" 8
y=^ nch2 chj "\j cha y = ^ nch2 chj "\ j cha
6469/H 6469 / H
85 85
86 86
Beispiel Diazokomponente Kupplungskomponente Example diazo component coupling component
Quaternierungsmittel Quaternizing agent
Farbton auf Polyacrylnitril Color on polyacrylonitrile
359 359
owc owc
è è
CH,, NHj CH ,, NHj
360 360
0CHa 0CHa
/c2h8 / c2h8
0^ch,CH,-@ 0 ^ ch, CH, - @
OCH, OCH,
OC, H, OC, H,
0 0
^chgchg-f^ NHCOCHb ^ chgchg-f ^ NHCOCHb
(y> o2oc2h5 (y> o2oc2h5
Bordo Bordo
Bordo Bordo
361 361
363 363
vt^v /c*h« vt ^ v / c * h «
S^chgch,/^ S ^ chgch, / ^
cl x=/ cl x = /
/ca hs / ca hs
/-\ >chj| -^3 / - \> chj | - ^ 3
o" ^ch,/3 o "^ ch, / 3
(ch30)2s02 (ch30) 2s02
(ch3o)2so2 (ch3o) 2so2
Rot red
Rot red
Rot red
364 364
XE) XE)
O\ch,.0 O \ ch, .0
(CH3o)2so2 (CH3o) 2so2
Rot red
365 365
J7~\ xcth8 ^c^i ch^ J7 ~ \ xcth8 ^ c ^ i ch ^
(CH3o)2so2 (CH3o) 2so2
Rot red
366 366
/—v /chj-^3 / —V / chj- ^ 3
(ch3o)2so2 (ch3o) 2so2
Rot red
367 367
©■< © ■ <
/ch, / ch,
cha cha
(ch30)2s02 (ch30) 2s02
Rot red
6469/73 6469/73
87 87
88 88
Beispiel Diazokomponente Kupplungskomponente Example diazo component coupling component
Quaternierungsmittel Quaternizing agent
Farbton auf Polyacrylnitril Color on polyacrylonitrile
*cp * cp
368 n^-nh, 368 n ^ -nh,
Ù Ù
369 369
PV-© PV- ©
CH. CH.
p./ch,c^cm p./ch,c^cm
CH, CH,
SCH»-© SCH »- ©
(ch30)2s02 (ch30) 2s02
(ch3o)2so2 (ch3o) 2so2
Rot red
Rot red
370 370
f>k'ckl "Q f> k'ckl "Q
ci^ ci ^
(ch3o)2so2 (ch3o) 2so2
Rot red
371 371
^C^ch,-© ^ C ^ ch, - ©
chj w chj w
(ch30)2s02 (ch30) 2s02
Rot red
372 372
H" H"
NHCOCHj NHCOCHj
(ch30)2s02 (ch30) 2s02
Rot red
373 373
374 374
chg ^ chg ^
ocha ok
Kn/c#h#^ Kn / c # h # ^
>=/ sch«-0 > = / sch «-0
N HC OC Hg X=/ N HC OC Hg X = /
(ch3o)2so2 (ch3o) 2so2
(ch30)2s02 (ch30) 2s02
Bordo Bordo
Bordo Bordo
375 375
n&nh, n & nh,
XN' XN '
i i
CH« CH «
376 376
0"nv 0 "na
/C,H, / C, H,
ch,-^ ch, - ^
o-< o- <
ch.-0* ch.-0 *
chj chj
(ch3o)2so2 (ch3o) 2so2
(ch30)2s02 (ch30) 2s02
Orange orange
Orange orange
6469/73 6469/73
Beis] By S]
377 377
378 378
379 379
380 380
381 381
382 382
383 383
384 384
385 385
89 89
90 90
Diazokomponente Kupplungskomponente Quaternierungsmittel Diazo component coupling component quaternizing agent
Xl> Xl>
CKch, ^ CKch, ^
cha cha
(=/ nch.CH.-Q (= / nch.CH.-Q
^./ch> •© ^. / ch> • ©
sc^chj sc ^ chj
(ch3o)2so2 (ch3o) 2so2
(CH3o)2so2 (CH3o) 2so2
(CH3o)2so2 (CH3o) 2so2
(CH30)2S02 cl c,h^ (CH30) 2S02 cl c, h ^
(CH30)2S02 (CH30) 2S02
/7-\ / 7- \
P"v-© P "v- ©
cha cha
-CHj CH, CN -CHj CH, CN
(CH30)2S02 (CH30) 2S02
' ^ch, _v ch, '^ ch, _v ch,
Pvo chj Pvo chj
P"v-0 P "v-0
(CH30)2S02 (CH30) 2S02
' CH, -v_v cha 'CH, -v_v cha
^<ccch, <3 ,c"'0hs0' ^ <ccch, <3, c "'0hs0'
chg chg
/c,h, / c, h,
(CH30)2S02 (CH30) 2S02
P"n'i'-0 P "n'i'-0
NHCOCHa NHCOCHa
6469/73 6469/73
Beis] By S]
386 386
387 387
388 388
389 389
390 390
391 391
392 392
393 393
394 394
91 91
92 92
Diazokomponente Diazo component
Kupplungskomponente Coupling component
Ouaternierungsmittel Ouaternizing agent
«.ce«. ".Ce".
ck, ck,
h, c ch» n^-nh, h, c ch »n ^ -nh,
i i
CH, CH, CN CH, CH, CN
och5 och5
(' nVN ('nVN
CH,, CH ,,
^ch,-^ ^ ch, - ^
0chs 0chs
/rC 'C*H® / rC 'C * H®
p v -o p v -o
NHCOCHg x=/ NHCOCHg x = /
/CaH» / CaH »
CK CK
'chj 'chj
-o -O
(ch30)2s02 (ch30) 2s02
(ch30)2s02 (ch30) 2s02
(ch30)2s02 (ch30) 2s02
r-\ ^CH, r- \ ^ CH,
o<^n o <^ n
(ch30)2s02 (ch30) 2s02
Xi) Xi)
(ch30)2s02 (ch30) 2s02
/7~\ /'c«h5 >=/ NVCH, CH, / 7 ~ \ / 'c «h5> = / NVCH, CH,
/-\ ych,0 / - \ ych, 0
yc*h6 yc * h6
cha cha
6469/73 6469/73
(CH30)2S02 (CH30) 2S02
Beisi Beisi
395 395
396 396
397 397
398 398
399 399
400 400
401 401
402 402
403 403
93 93
94 94
Diazokomponente Kupplungskomponente Diazo component coupling component
Ouaternierungsmittel Ouaternizing agent
HgC CHg i HgC CHg i
CHg CH. CN CHg CH. CN
p^chgchgcn chs p ^ chgchgcn chs
QV-o QV-o
(ch3o)2so2 (ch3o) 2so2
(ch30)2s02 (ch30) 2s02
ckc,h' ^ ckc, h '^
xchgchg-^v cha ^ xchgchg- ^ v cha ^
(ch30)2s02 (ch30) 2s02
hbc chg n^-nh, hbc chg n ^ -nh,
i ch,-^2> i ch, - ^ 2>
/-?k 'c*hb / -? k 'c * hb
NHCOCHa NHCOCHa
0CI% 0CI%
jr-rf /Ct H8 jr-rf / Ct H8
CH,, X=/ CH ,, X = /
OCH, yy^ /^2 hg OCH, yy ^ / ^ 2 hg
PV <3 PV <3
NHCOCHg X=/ NHCOCHg X = /
o-<c,h' o- <c, h '
ch,-© ch, - ©
(ch3o)2so2 (ch3o) 2so2
(ch30)2s02 (ch30) 2s02
(ch3o)2so2 (ch3o) 2so2
ch2=ch-conh2 ch2 = ch-conh2
ch2=ch-conh2 ch2 = ch-conh2
Xi) avo Xi) avo
6469/73 6469/73
ch,=ch-conh2 ch, = ch-conh2
Beis By S
404 404
405 405
406 406
407 407
408 408
409 409
410 410
411 411
412 412
95 95
96 96
Diazokomponente Kupplungskomponente Quaternierungsmittel h.c ch, ~ Diazo component coupling component quaternizing agent h.c ch, ~
ch..ch-conh, ch..ch-conh,
ch."© ch. "©
r-\ ✓cha'c^ ©"^ch.ch-© r- \ ✓cha'c ^ © "^ ch.ch- ©
ch2=ch-conh2 ch2 = ch-conh2
cha "d^cl ch2=ch-conh2 cha "d ^ cl ch2 = ch-conh2
' C* H* 'C * H *
chg w ch2=ch-conh2 chg w ch2 = ch-conh2
f^/chac^cm f ^ / chac ^ cm
>* ^ch>%f% cha na=/ > * ^ ch>% f% cha na = /
"o "O
W XCH chs ^ W XCH chs ^
ch2=ch-cooch, ch2 = ch-cooch,
ch2=ch-cooch3 ch2 = ch-cooch3
/twc'h» _ / twc'h »_
vch,-0> vch, -0>
CH, W CH, W
ch2=ch-COOCHj ch2 = ch-COOCHj
/r\ 'C*H® / r \ 'C * H®
NHCOCHj NHCOCHj
/>«% /> «%
/rL 'c*h* p" -ch. -© / rL 'c * h * p "-ch. - ©
chg ^ chg ^
ch2=ch-cooch3 ch2 = ch-cooch3
ch2=ch-cooch, ch2 = ch-cooch,
6469/73 6469/73
Beis] By S]
413 413
414 414
415 415
416 416
417 417
418 418
419 419
420 420
421 421
97 97
98 98
Diazokomponente Kupplungskomponente Quaternierungsmittel Farbton auf Diazo component coupling component quaternizing agent color
Polyacrylnitril hec ch. ocha Polyacrylonitrile hec ch. ok
»tu kn;c'h' »Do kn; c'h '
V-/ .. CH2=CH-COOCH3 blaust. Rot cha-0 V- / .. CH2 = CH-COOCH3 bluish. Red cha-0
hscch, hscch,
ù ù
NHC0CHa NHC0CHa
/cahb / cahb
ckg -^3 ckg - ^ 3
XE) XE)
O v ■© O v ■ ©
(CH30)2S02 gelbst. Rot (CH30) 2S02 yellow. red
(CH30)2S02 gelbst. Rot (CH30) 2S02 yellow. red
(CH30)2S02 gelbst. Rot (CH30) 2S02 yellow. red
CM CM
✓ c,h, ✓ c, h,
^chsjcha •© ^ chsjcha • ©
/—v ✓ch2-^3 0-<CVt^Q / —V ✓ch2- ^ 3 0- <CVt ^ Q
\=/ s chg \ = / s chg
(CH30)2S02 gelbst. Rot (CH30) 2S02 yellow. red
(CH30)2S02 gelbst. Rot (CH30) 2S02 yellow. red
(CH30)2S02 gelbst. Rot (CH30) 2S02 yellow. red
Beisf Example
422 422
423 423
424 424
425 425
426 426
427 427
428 428
429 429
430 430
99 99
100 100
Diazokomponente Kupplungskomponente Quaternierungsmittel Diazo component coupling component quaternizing agent
ôN ôN
n»0 en» chs/ta n »0 en» chs / ta
<n>nh, f\k (ch30)2s02 <n> nh, f \ k (ch30) 2s02
>=/ -ch.-o chjj w > = / -ch.-o chjj w
>c2h8 > c2h8
CHg -^3 CHg - ^ 3
ch, w ch, w
/f-\ 'ca1*« / f- \ 'ca1 * «
£>V-0 £> V-0
NHCOCHs NHCOCHs
ÇKs* ■© ÇKs * ■ ©
cha w ocha rC 'C*H» cha w ocha rC 'C * H »
P" V -O P "V -O
NHC0CHs h>c ch» NHC0CHs h> c ch »
N^-nh, 0-<c'*'-0 N ^ -nh, 0- <c '*' - 0
n^s n ^ s
Ö Ö
w - ^ch,^ w - ^ ch, ^
& &
(Ko i—v ✓CfH« (Ko i — v ✓CfH «
O-vc^-o O-vc ^ -o
(ch30)2s02 (ch30) 2s02
(ch3o)2so2 (ch3o) 2so2
(ch30)2s02 (ch30) 2s02
(ch30)2s02 (ch30) 2s02
(ch30)2s02 (ch30) 2s02
(œ3o)2so2 (œ3o) 2so2
(ch3o)2so2 (ch3o) 2so2
(CH30)2S02 (CH30) 2S02
6469/73 6469/73
Beis By S
431 431
432 432
433 433
434 434
435 435
436 436
437 437
438 438
439 439
101 101
102 102
Diazokomponente Diazo component
Kupplungskomponente Coupling component
Quaternierungsmittel Quaternizing agent
*° c* * ° c *
n^-nha n^s n ^ -nha n ^ s
ë ë
schac^ schac ^
/tsv 'ch» / tsv 'ch »
O^cn, -©-( O ^ cn, - © - (
✓ c2 h# ✓ c2 h #
(ch30)2s02 (ch30) 2s02
(ch3o)2so2 (ch3o) 2so2
(ch30)2s02 (ch30) 2s02
p./0H»CH*CN p./0H timeCH*CN
ch, ch,
v=h,-0 v = h, -0
(ch3o)2so2 (ch3o) 2so2
fv°* "q y=j xcht^ fv ° * "q y = j xcht ^
(ch30)2s02 (ch30) 2s02
c2h8 c2h8
CHj CHj
CHa CHa Cha Cha
(ch30)2s02 (ch30) 2s02
«tv/08"8 vch,-© «Tv / 08" 8 vch, - ©
NHCOCHa NHCOCHa
(ch30)2s02 (ch30) 2s02
OCH, /r-£ xc2 h8 OCH, / r- £ xc2 h8
kv-o kv-o
CH,, W CH ,, W
(ch30)2s02 (ch30) 2s02
£ £
0CHs /c8h8 0CHs / c8h8
=^ch, o urnru \r=y = ^ ch, o urnru \ r = y
NHCOCHa NHCOCHa
6469/73 6469/73
(CH3o)2so2 (CH3o) 2so2
Beis[ By S[
440 440
441 441
442 442
443 443
444 444
445 445
446 446
447 447
448 448
103 103
104 104
Diazokomponente Kupplungskomponente Ouaternierungsmittel h,c chg Diazo component coupling component ouating agent h, c chg
©<£© © <£ ©
è è
w w
\=/ -^3 \ = / - ^ 3
/E) / E)
/c2hs / c2hs
'^chj, cha *^3 '^ chj, cha * ^ 3
^ .cha/3 ^ .cha / 3
CKc^cVb y*"*, 'ch» CKc ^ cVb y * "*, 'ch»
^cHa^Cl ^ cHa ^ Cl
✓ ca h5 ✓ ca h5
SKh,-© SKh, - ©
CHa W CHa W
^chachacn ^ chachacn
P^-o f>/ckî >=' "c^-o cu w P ^ -o f> / ckî> = '"c ^ -o cu w
6469/73 6469/73
(ch30)2s02 (ch30) 2s02
(ch30)2s02 (ch30) 2s02
(CH3o)2so2 (CH3o) 2so2
(ch30)2s02 (ch30) 2s02
(ch30)2s02 (ch30) 2s02
(chs0)2s02 (chs0) 2s02
(ch30)2s02 (ch30) 2s02
(ch3o)2so2 (ch3o) 2so2
(ch3o)2so2 (ch3o) 2so2
Beisp Ex
449 449
450 450
451 451
452 452
453 453
454 454
455 455
456 456
457 457
105 105
106 106
Diazokomponente Kupplungskomponente Quaternierungsmittel hg c chs, Diazo component coupling component quaternizing agent hg c chs,
-o -O
0 0
'c2 ha 'c2 ha
PV -© PV - ©
H8c, CHa i-cah, H8c, CHa i-cah,
ocha ok
/cahfl / cahfl
-en -o cha w -en -o cha w
OCHa OCHa
/r£ / r £
p v -0 p v -0
mur-nru \=i/ mur-nru \ = i /
NHCOCHg NHCOCHg
. . . . . .
©< © <
cha "\_j cha "\ _j
'ch, -v3 'ch, -v3
^ XE> ^ XE>
CKch, -© CKch, - ©
ä-n. /caha a-n. / caha
/—\ ✓cha-^3 / - \ ✓cha- ^ 3
o^<c,cro o ^ <c, cro
(ch30)2s02 (ch30) 2s02
(CH3o)2so2 (CH3o) 2so2
(CH3o)2so2 (CH3o) 2so2
(ch30)2s02 (ch30) 2s02
(ch3o)2so2 (ch3o) 2so2
(ch30)2s02 (ch30) 2s02
(ch30)2s02 (ch30) 2s02
(ch3o)2so2 (ch3o) 2so2
(CH30)2S02 (CH30) 2S02
6469/73 6469/73
Beisf Example
458 458
459 459
460 460
461 461
462 462
463 463
464 464
465 465
466 466
107 107
108 108
Diazokomponente Kupplungskomponente Quaternierungsmittel Diazo component coupling component quaternizing agent
HsCa CH, HsCa CH,
m-nh, fvch* _ m-nh, fvch * _
^ sch,-<^-cl i ^ sch, - <^ - cl i
i-c^ i-c ^
l^C CHa l ^ C CHa
/7~\ 'cahs ch, w / 7 ~ \ 'cahs ch, w
^/ch,0hch ^ / ch, 0hch
„ 'C»H. "'C» H.
CH, CH,
-CHj CHj, CN -CHj CHj, CN
7n> 7n>
cha en w fvc* "■ _ cha en w fvc * "■ _
cha ^ cha ^
PC-o PC-o
✓c.h, ✓c.h,
v v
NHCOCHg ocha NHCOCHg ok
H ✓C.H. H ✓C.H.
chg ocha xcaha chg ocha xcaha
NHCOCHj NHCOCHj
&-■ oC© & - ■ oC ©
(ch30)2s02 (ch30) 2s02
(ch3o)2so2 (ch3o) 2so2
(ch30)2s02 (ch30) 2s02
(ch30)2s02 (ch30) 2s02
(CH30)2S02 (CH30) 2S02
(ch30)2s02 (ch30) 2s02
(ch30)2s02 (ch30) 2s02
(ch30)2s02 (ch30) 2s02
(ch30)2s02 (ch30) 2s02
6469/73 6469/73
109 109
110 110
Beispiel Diazokomponente Kupplungskomponente Example diazo component coupling component
Quaternierungsmittel Quaternizing agent
Farbton auf Polyacrylnitril Color on polyacrylonitrile
467 467
n^-nh, n ^ -nh,
0,0 0.0
468 468
/-\ / - \
/E) / E)
(ch30)2s02 (ch30) 2s02
(ch3o)2so2 (ch3o) 2so2
Orange orange
Orange orange
469 469
©-h © -h
,C,H, , C, H,
nchach2-0 nchach2-0
(ch30)2s02 (ch30) 2s02
Orange orange
470 470
(ch30)2s02 (ch30) 2s02
Orange orange
471 471
/chb /CH B
(/ \>N (/ \> N
nch»"^3"c1 nch »" ^ 3 "c1
(ch30)2s02 . (ch30) 2s02.
Orange orange
472 472
/7~\ ' C* H# en w / 7 ~ \ 'C * H # en w
(ch30)2s02 (ch30) 2s02
gelbst. Rot yellow. red
473 473
^ ^chacncn ^ ^ chacncn
(CH3o)2so2 (CH3o) 2so2
gelbst. Rot yellow. red
474 474
<TVc"Hb^ <TVc "Hb ^
CH3 \=/ CH3 \ = /
(ch3o)2so2 (ch3o) 2so2
gelbst. Rot yellow. red
475 475
fVc*Hj ^ fVc * Hj ^
chj w chj w
6469/73 6469/73
(ch30)2s02 (ch30) 2s02
gelbst. Rot yellow. red
Beisp Ex
476 476
477 477
478 478
479 479
480 480
481 481
482 482
483 483
484 484
111 111
112 112
Diazokomponente Kupplungskomponente Quaternierungsmittel Diazo component coupling component quaternizing agent
Hg C CHb Hg C CHb
NHCOCHb ocha NHCOCHb ok
'C*H» 'C * H »
P"v-0 P "v-0
ch3 w ocha ch3 w ocha
NHCOCHg NHCOCHg
^-nhch, ^ -nhch,
ô O
NHCHg O NHCHg O
cha cha
^^-nhcha Cl ^^ - nhcha Cl
(ch30)2s02 (ch30) 2s02
(ch30)2s02 (ch30) 2s02
(ch3o)2so2 (ch3o) 2so2
(ch3o)2so2 (ch3o) 2so2
(ch30)2s02 (ch30) 2s02
(ch30)2s02 (ch30) 2s02
(ch30)2s02 (ch30) 2s02
ocha en ok
(ch30)2s02 (ch30) 2s02
^ch,-0 ^ ch, -0
/ca ha / ca ha
< >n (ch30)2s02 <> n (ch30) 2s02
n=/^ch,-0 n = / ^ ch, -0
6469/73 6469/73
Beis] By S]
485 485
486 486
487 487
488 488
489 489
490 490
491 491
492 492
493 493
494 494
113 114 113 114
Diazokomponente Kupplungskomponente Quaternierungsmittel o Diazo component coupling component quaternizing agent o
/c4h, / c4h,
ch»"0 ch »" 0
O-h y© O-h y ©
^oh,-Q ^ oh, -Q
en en
'C, H 'C, H
/t~\\ / t ~ \\
(ch3o)2so2 (ch3o) 2so2
(ch30)2s02 (ch30) 2s02
(ch3o)2so2 (ch3o) 2so2
(CH3o)2so2 (CH3o) 2so2
(CH3o)2so2 (CH3o) 2so2
(ch30)2s02 (ch30) 2s02
(ch3o)2so2 (ch3o) 2so2
w "en-o w "en-o
NO, NO,
^-NHCH, CH, H^^^-SOpCHj ^ -NHCH, CH, H ^^^ - SOpCHj
6469/73 6469/73
Beis By S
495 495
496 496
497 497
498 498
499 499
500 500
501 501
502 502
503 503
504 504
115 115
116 116
Diazokomponente Kupplungskomponente Quaternierungsmittel Diazo component coupling component quaternizing agent
S- S-
Ò O
chg chg
^2 (Ì nVn' r-^ (CH30)jS02 ^ 2 (Ì nVn 'r- ^ (CH30) jS02
QCo ru \=J QCo ru \ = J
chg chg
>r^wct h» > r ^ wct h »
K V o K V o
Cl ocha nhcoch ocn w /ca h. Cl ocha nhcoch ocn w / ca h.
KVO KVO
ch. x=y ch. x = y
/c4 hp / c4 hp
P V o P V o
/c4hp / c4hp
►k cha eCo ►k cha eCo
/ïh.ch.oh /ïh.ch.oh
(CH30)2S02 (CH30) 2S02
(CH30)2S02 (CH30) 2S02
/—TV /c« ha / —TV / c «ha
V n>N (C2H5O)2SO2 V n> N (C2H5O) 2SO2
(C2H50)2S02 (C2H50) 2S02
ocha ri.v Cz H® __ (C2H50)2S02 ocha ri.v Cz H® __ (C2H50) 2S02
ocf* n—f och, ocf * n — f och,
nhcoc2h5 x—' nhcoc2h5 x— '
C2H50)2S02 C2H50) 2S02
(c2h5o)2so2 (c2h5o) 2so2
C,H,Br C, H, Br
C2H5Br C2H5Br
6469/73 6469/73
117 117
118 118
Beispiel Diazokomponente Kupplungskomponente Quaternierungsmittel Farbton auf Example diazo component coupling component quaternizing agent color
Polyacrylnitril Polyacrylonitrile
/cn / cn
Y Y
505 X)-N' ~ /^XCE, C2H5Br gelbst. Rot 505X) -N '~ / ^ XCE, C2H5Br yellow. red
ô 0 ô 0
506 506
508 508
511 511
512 512
/t\.'ch*ch*nhc0ch3 /t\.'ch*ch*nhc0ch3
C2H5Br gelbst. Rot chs C2H5Br yellow. Red chs
✓CH,CH,NHS0, ✓CH, CH, NHS0,
" \ C2H5Br gelbst. Rot nhf CH, CH, NHCO "\ C2H5Br yellow. Red nhf CH, CH, NHCO
^ch.<0> ^ ch. <0>
C2H5Br gelbst. Rot C2H5Br yellow. red
^ .chjchgnhco-^ ^ .chjchgnhco- ^
509 » \> y-N C2H5Br gelbst. Rot 509 »\> y-N C2H5Br yellow. red
CH»vJ CH »vJ
/r-^ , CH, CHg NHC0-^~^VC] / r- ^, CH, CHg NHC0- ^ ~ ^ VC]
510 V 7-N yr-^ C2H5Br gelbst. Rot 510 V 7-N yr- ^ C2H5Br yellow. red
'ch2 \_7 'ch2 \ _7
7cn CH, OC OC Ha 7cn CH, OC OC Ha
X°=-' NCH, X ° = - 'NCH,
(CH30)2S02 gelbst. Rot (CH30) 2S02 yellow. red
/Tiv /CH, CH, OCn Cn OH / Tiv / CH, CH, OCn Cn OH
\=y (CH30)2S02 gelbst. Rot \ = y (CH30) 2S02 yellow. red
/T-rv /CHa CH„ OCOOCH,, / T-rv / CHa CH „OCOOCH ,,
513 " \ /*N /T~Tv (CH30)2S02 gelbst. Rot 513 "\ / * N / T ~ Tv (CH30) 2S02 yellow. Red
CH, V-v CH, V-v
514 514
■ttv /chj ci4 och, ■ ttv / chj ci4 och,
\ _ (/*"N ,r—-v (CH30)2S02 gelbst. Rot n ' nchj \ _ (/ * "N, r —- v (CH30) 2S02 yellow. Red n 'nchj
6469/73 6469/73
Beis By S
515 515
516 516
517 517
518 518
519 519
520 520
521 521
522 522
523 523
119 119
120 120
Diazokomponente Kupplungskomponente Quaternierungsmittel Diazo component coupling component quaternizing agent
ô ° ô °
o< o <
/cnchjcooch c,i-0 / cnchjcooch c, i-0
h.c^o.0 h.c ^ o.0
jr-~ xch.ch.cl jr- ~ xch.ch.cl
O^-o O ^ -o
(ch30)2s02 (ch30) 2s02
(ch3o)2so2 (ch3o) 2so2
f-/chgch^sogcn f- / chgch ^ sogcn
CvnvcH, Ô (CH>0),S°! CvnvcH, Ô (CH> 0), S °!
(ch30)2s02 (ch30) 2s02
(CH3o)2so2 (CH3o) 2so2
r—v /CHg CHg CH^ Cl (ch3o)2so2 r-v / CHg CHg CH ^ Cl (ch3o) 2so2
Okch,<G> Okch, <G>
__ /CH, CHg 0C0CHÂ/3 0 \\-n 1 (ch3o)2so2 __ / CH, CHg 0C0CHÂ / 3 0 \\ - n 1 (ch3o) 2so2
w nchg-0 w nchg-0
/—. ,CHg CHg 0C0N(Cn )g / -. , CHg CHg 0C0N (Cn) g
0"?ch, -Q) ,ch,0)'s°! 0 "? Ch, -Q), ch, 0) 's °!
/CHg CHg CN / CHg CHg CN
k v-n /--v (ch30)2s02 k v-n / - v (ch30) 2s02
^=^^chg •^^"cl ^ = ^^ chg • ^^ "cl
6469/73 6469/73
121 121
122 122
Beispiel Diazokomponente Example diazo component
Kupplungskomponente Coupling component
Quaternierungsmittel Farbton auf Quaternizing agent shade
Polyacrylnitril Polyacrylonitrile
«4 n^nh, «4 n ^ nh,
Ù Ù
525 525
ch»-0 ch »-0
NO, NO,
/(CH, )SN(C,H#), / (CH,) SN (C, H #),
vch2-0 vch2-0
(ch30)2s02 (ch30) 2s02
(ch30)2s02 (ch30) 2s02
gelbst. Rot gelbst. Rot yellow. Red yellow. red
526 526
527 527
-V XH, CH-OCONH-^3 -V XH, CH-OCONH- ^ 3
V^T * \=/ (CH5o)2so2 V ^ T * \ = / (CH5o) 2so2
fy fy
s^\nh-chacn -^3 s ^ \ nh-chacn - ^ 3
Cl Cl
(ch30)2s02 (ch30) 2s02
gelbst. Rot yellow. red
Orange orange
528 528
529 529
530 530
/f^v /c*h» / f ^ v / c * h »
>=/ NnCH,CH, > = / NnCH, CH,
ch3 ch3
„ Xi> "Xi>
(ch30)2s02 (ch30) 2s02
ch3c1 ch3c1
ch3ci ch3ci
Rot gelbst. Rot gelbst. Rot Red yellow. Red yellow. red
531 531
532 532
533 533
^ /CH, CH, CN \=/'^ CH, CH, ^ / CH, CH, CN \ = / '^ CH, CH,
/7~\ /c2h5 / 7 ~ \ / c2h5
P'ch.CH,^) P'ch.CH, ^)
iiurrvw^ \r=/ iiurrvw ^ \ r = /
NHCOCHg NHCOCHg
Ç> Ç>
CH, CH,
/CK, / CK,
^ch, ^ ch,
ch3c1 ch3c1
gelbst. Rot blaust. Rot yellow. Red bluish. red
Rot red
6469/73 6469/73
123 123
124 124
534 534
Rot red
Beispiel Diazokomponente Kupplungskomponente Quaternierungsmittel Farbton auf Example diazo component coupling component quaternizing agent color
Polyacrylnitril Polyacrylonitrile
S* S *
ò O
s-* xCH,Cn OH s- * xCH, Cn OH
535 * S=/%h.^ 535 * S = /% h. ^
CH, CH,
^CH,CH,N(C,H„), ^ CH, CH, N (C, H „),
536 pvo chj r—v / CÜ2 CHj NHCHO 536 pvo chj r-v / CÜ2 CHj NHCHO
537 „ V NVn yj-jv „ Rot 537 "V NVn yj-jv" Red
,cnch,sq,ch, , cnch, sq, ch,
538 • HVO 538 • HVO
cr^ cr ^
^CH, Cn NHSO, Ct H5 ^ CH, Cn NHSO, Ct H5
539 - ( rn " rot en 539 - (rn "rot en
PyCHj CH, NHCONHCHb PyCHj CH, NHCONHCHb
\H, O en x=/ \ H, O en x = /
/CH. CH, NHCO-0-CH, / CH. CH, NHCO-0-CH,
w'ch, -0) w'ch, -0)
541 Rot en 541 red
/r^\ /cncnococgh, / r ^ \ / cncnococgh,
542 „ (' V"N /r-T\ „ Rot 542 "('V" N / r-T \ "Red
\=y s, \ = y s,
en w oc», en w oc »,
/j~~\ ^enenoenen / j ~~ \ ^ enenoenen
Pv-o Pv-o
543 Rot en 543 red
6469/73 6469/73
125 125
126 126
Beispiel Diazokomponente Kupplungskomponente Quaternierungsmittel Farbton auf Example diazo component coupling component quaternizing agent color
Polyacrylnitril Polyacrylonitrile
544 544
546 546
547 547
552 552
6 6
2-*2 opcft ro. 2- * 2 opcft ro.
.CILCHa OC Hb .CILCHa OC Hb
545 » (f W Av „ Rot 545 »(f W Av" Red
/J-\\ /ungufiaw / J - \\ / ungufiaw
P<™.<2> P <™. <2>
cha w cha w
© /7~\ /ch, ce, 0-^3 © / 7 ~ \ / ch, ce, 0- ^ 3
•g-™- $> v • g- ™ - $> v
0 r" 0 r "
— xch,cnc0 - xch, cnc0
PV-ö PV-ö
(CH30)2S02 Rot (CH30) 2S02 red
CH, CH,
/CHaCHaCOOCj H„ / CHaCHaCOOCj H "
m-n cha n /—n \=/ m-n cha n / —n \ = /
(CH30)2S02 Rot (CH30) 2S02 red
/t~\\. /vnjv/nj ou / t ~ \\. / vnjv / nj ou
P^O P ^ O
548 " / Nv ___ /7~\ (CH30)2S02 Rot ch, 548 "/ Nv ___ / 7 ~ \ (CH30) 2S02 red ch,
/CHa CHg Cl / CHa CHg Cl
549 » (' N>N /^\ (CH30)2S02 Rot 549 »('N> N / ^ \ (CH30) 2S02 red
/t^t^ 2-t cc vchs "o / t ^ t ^ 2-t cc vchs "o
/CHg CHa CHa Br / CHg CHa CHa Br
550 » <f V"N (CH30)2S02 Rot y=J vcha ft'br ch, v=/ 550 »<f V" N (CH30) 2S02 red y = J vcha ft'br ch, v = /
-r-a ,cn c^ ococha-^3 -r-a, cn c ^ ococha- ^ 3
551 <f y-n >7-^ (CH30)2S02 Rot 551 <f y-n> 7- ^ (CH30) 2S02 red
>=/^cn^> > = / ^ cn ^>
\ssJ \ ssJ
cha cha
/chachaoconccil )2 / chachaoconccil) 2
/TVyij Av (CH30)2S02 / TVyij Av (CH30) 2S02
v -ch.-0 v -ch.-0
'W XZZJ 'W XZZJ
ch3 ch3
A s\ An® V/iij US A s \ An® V / iij US
P'ch, A P'ch, A
chj ^ chj ^
Rot red
.chg chg 0s0# n(cn )ß .chg chg 0s0 # n (cn) ß
553 >N (CH30)2S02 Rot 553> N (CH30) 2S02 red
6469/73 6469/73
Beis: By S:
554 554
555 555
556 556
557 557
558 558
559 559
560 560
561 561
562 562
563 563
127 128 127 128
Diazokomponente Kupplungskomponente Quaternierungsmittel rk /r^ 'ch»ch*cn Diazo component coupling component quaternizing agent rk / r ^ 'ch »ch * cn
NHj, V-/Nv /t\ (CH3o)2so2 NHj, V- / Nv / t \ (CH3o) 2so2
Ô O
W N-CH, Od ch5 w W N-CH, Od ch5 w
,(CH, ), N(CH, ), , (CH,), N (CH,),
PVQ PVQ
"u >—J "u> —J
(CH30)2S02 (CH30) 2S02
ch3 ch3
,CH» CH» 0C0NH*\/*C1 , CH »CH» 0C0NH * \ / * C1
Çr'-^JQ W Çr '- ^ JQ W
(CH30)2S02 (CH30) 2S02
^ch, ^ ch,
^3"nhcha ochg cht "^3 ^ 3 "nhcha ochg cht" ^ 3
cl cl
<^)-nhchb cha -tQ) <^) - nhchb cha -tQ)
chg chg
^j^-nh-chjj chsj 0chs r-J£> ^ j ^ -nh-chjj chsj 0chs r-J £>
o"201 o "201
chg w fvch* "® chg w fvch * "®
>=/ ^chgcha^f ^ > = / ^ chgcha ^ f ^
chj chj
6469/73 6469/73
Beis] By S]
564 564
565 565
566 566
567 567
568 568
569 569
570 570
571 571
572 572
573 573
129 129
130 130
Diazokomponente Diazo component
Kupplungskomponente Coupling component
Quaternierungsmittel Quaternizing agent
S- S-
ô O
onn i onn i
cha cha
/-ci^chgcn p"n^ch2ch20 :H3 W / -ci ^ chgcn p "n ^ ch2ch20: H3 W
ocha w /c*h» w-cncn/3 ocha w / c * h »w-cncn / 3
r VS/ r VS /
CH. CH.
0 0
OC H, OC H,
OCHj, OCHj,
/c2h8 / c2h8
=/^ch,cno i TJ Va»/ = / ^ ch, cno i TJ Va »/
,00, h, 00 h
•=' ^cnch, -^3 • = '^ cnch, - ^ 3
nhcocha z0*11» nhcocha z0 * 11 »
P"\nch,-© P "\ nch, - ©
Cl Cl
/cah8 / cah8
^=^nscn -o ch, w ^ = ^ nscn -o ch, w
<>C© <> C ©
o-< o- <
CHg CHg
CHa "v3 CHa "v3
_ Xl> 0-v-© _ Xl> 0-v- ©
Qch2ci Qch2ci
(CH30)2S02 (CH30) 2S02
(CH30)2S02 (CH30) 2S02
(CHj0)2S02 (CHj0) 2S02
(CH30)2S02 (CH30) 2S02
/cahg / cahg
>=' ^chacn-^^ > = '^ chacn - ^^
6469/73 6469/73
(CH,0)2S02 (CH, 0) 2S02
Beis By S
574 574
575 575
576 576
577 577
578 578
579 579
580 580
581 581
582 582
131 131
132 132
Diazokomponente Kupplungskomponente Quaternierungsmittel Diazo component coupling component quaternizing agent
»e?© »E? ©
/r\ 'CI^ / r \ 'CI ^
<o-voci <o-voci
/ iy / C® H. / iy / C® H.
CHa CHa
^ ^ch^cn ^ ^ ch ^ cn
SX«.-© SX «.- ©
r>u \IT/ r> u \ IT /
rvchj y=y ^ ch^-O rvchj y = y ^ ch ^ -O
CHS W CHS W
'C*H® 'C * H®
P V o P V o
NHCOCHj ^— NHCOCHj ^ -
OC H, OC H,
xcahe w1^ -o xcahe w1 ^ -o
CH, W CH, W
ocha ok
/rC 'C*H® / rC 'C * H®
-o -O
NHCOCHj V-/ NHCOCHj V- /
(CH30)2S02 (CH30) 2S02
(CH30)2S02 (CH30) 2S02
(CH30)2S02 (CH30) 2S02
(CH30)2S02 (CH30) 2S02
(CH30)2S02 (CH30) 2S02
(CH3o)2so2 (CH3o) 2so2
(CH30)2S02 (CH30) 2S02
(CH30)2S02 (CH30) 2S02
(CH30)2S02 (CH30) 2S02
6469/73 6469/73
Beis By S
583 583
584 584
585 585
586 586
587 587
588 588
589 589
590 590
591 591
133 133
134 134
Diazokomponente Kupplungskomponente Diazo component coupling component
Ouaternierungsmittel Ouaternizing agent
Farbton auf Polyacrylnitril i Color on polyacrylonitrile i
chaci^cn chaci ^ cn
<SK <SK
/c2h, / c2h,
ch,-© ch, - ©
(CH30)2S02 (CH30) 2S02
Orange orange
<GK <GK
cha -<(_ chj cha - <(_ chj
(CH30)2S02 (CH30) 2S02
Orange orange
/h) -© / h) - ©
(CH30)2S02 (CH30) 2S02
Orange orange
©» © »
✓ c2hb ✓ c2hb
^chgcha O ^ chgcha O
(CH30)2S02 (CH30) 2S02
Orange orange
0/CHj^s 0 / CHj ^ s
(CH30)2S02 (CH30) 2S02
Orange f\/ch5 Orange for ch5
ncha ncha
Cl Cl
(CH30)2S02 (CH30) 2S02
Orange orange
* ■ v / ca h. * ■ v / ca h.
cha cha
(CH30)2S02 (CH30) 2S02
rotst. Orange red orange
^chachacn ^ chachacn
P*- P * -
en w en w
>=/ ch,-© > = / ch, - ©
6469/73 6469/73
(CH3o)2so2 (CH3o) 2so2
(CH30)2S02 (CH30) 2S02
rotst. Orange rotst. Orange red Orange red. orange
Beisf Example
592 592
593 593
594 594
595 595
596 596
597 597
598 598
599 599
600 600
135 135
136 136
Diazokomponente Kupplungskomponente Quaternierungsmittel Diazo component coupling component quaternizing agent
S- S-
C H C H
n>lt * 6 >r-tv (ch30)2s02 n> lt * 6> r-tv (ch30) 2s02
CHg CHg CN Cil, CHg CHg CN Cil,
i-CjH^ i-CjH ^
/"a ^cah# / "a ^ cah #
P""ch,-0 P "" ch, -0
NHCOCHg NHCOCHg
.oc1 .oc1
ff-L h. ff-L h.
ck«, o cu, w ck «, o cu, w
OCHg fix'0'*' OCHg fix'0 '*'
)=S sch,-^3 ) = S sch, - ^ 3
NHCOCHg N=/ /Cj,Ha NHCOCHg N = / / Cj, Ha
O-^ch,-© O- ^ ch, - ©
— .en - .en
0"^ch,/3 0 "^ ch, / 3
Xi) Xi)
ä-tw y ^2 s 0"N\CHg CHg ä-tw y ^ 2 s 0 "N \ CHg CHg
/-x /cha-^^ / -x / cha - ^^
'CHg CHg 'CHg CHg
6469/73 6469/73
(ch30)2s02 (ch30) 2s02
(ch30)2s2 (ch30) 2s2
(ch30)2s02 (ch30) 2s02
(ch30)2s02 (ch30) 2s02
(ch3o)2so2 (ch3o) 2so2
(ch30)2s02 (ch30) 2s02
'C2 Ht 'C2 Ht
N'm>NH2 (/ \>N (ch3o)2so2 N'm> NH2 (/ \> N (ch3o) 2so2
(CH30)2S02 (CH30) 2S02
Beis; By S;
601 601
602 602
603 603
604 604
605 605
606 606
607 607
608 608
609 609
137 137
138 138
Diazokomponente Kupplungskomponente Quaternierungsmittel Diazo component coupling component quaternizing agent
Q-\ Q- \
! !
ì-c5h7 ì-c5h7
chg chg
CHa CHa
^ch^cn p*-«*-© ^ ch ^ cn p * - «* - ©
ch, w ch, w
/v0*1 ^ / v0 * 1 ^
p v -© p v - ©
chj w nchg chj ~\y chj ^ chj w nchg chj ~ \ y chj ^
'c» hj 'c »hj
NHCOCHjj NHCOCHjj
/-7\ 'CïHs / -7 \ 'CïHs
€h™ jrs ocn € h ™ jrs ocn
>HL /C«H# > HL / C «H #
0%% ^3 0 %% ^ 3
cil, w cil, w
.ocha .ocha
/rC 'C*H«> / rC 'C * H «>
NHCOCHg N—' /c2h, NHCOCHg N— '/ c2h,
<X£© <X £ ©
(ch30)2s02 (ch30) 2s02
(ch30)2s02 (ch30) 2s02
(ch30)2s02 (ch30) 2s02
(ch30)2s02 (ch30) 2s02
(ch30)2s02 (ch30) 2s02
(ch30)2s02 (ch30) 2s02
(ch30)2s02 (ch30) 2s02
(ch3o)2so2 (ch3o) 2so2
(ch3o)2so2 (ch3o) 2so2
6469/73 6469/73
Beisj Ex
610 610
611 611
612 612
613 613
614 614
615 615
616 616
617 617
618 618
139 139
140 140
Diazokomponente Kupplungskomponente Diazo component coupling component
Quaternierungsmittel nv-nh» Quaternizing agent nv-nh »
k"© k "©
O-\0H, -© O- \ 0H, - ©
(CH30)2S02 (CH30) 2S02
(CH3o)2so2 (CH3o) 2so2
©h © h
/-C,H. / -C, H.
^chgchg o s-\ /ch« *^3 ^ chgchg o s- \ / ch «* ^ 3
£K*cC«© £ K * cC «©
(CH30)2S02 (CH30) 2S02
(CH30)2S02 (CH30) 2S02
©< © <
/CK, / CK,
ch* O01 ch * O01
(CH30)2S02 (CH30) 2S02
✓ cjh, ✓ cjh,
p°w-© p ° w- ©
ch3 ch3
(CH3o)2so2 (CH3o) 2so2
^ /CHg CHg CN ^ / CHg CHg CN
Pv-o chs w Pv-o chs w
(CH30)2S02 (CH30) 2S02
(CH30)2S02 (CH30) 2S02
jf-\ ^cahs jf- \ ^ cahs
>=/" nchachg-^3 > = / "nchachg- ^ 3
chj w chj w
(CH30)2S02 (CH30) 2S02
6469/73 6469/73
141 141
142 142
Beispiel Diazokomponente Example diazo component
Kupplungskomponente Coupling component
Quaternierungsmittel Quaternizing agent
Farbton auf Polyacrylnitril Color on polyacrylonitrile
619 619
nhj cha-0 nhj cha-0
620 620
621 621
/r\ hb NHCOCHa V=/ / r \ hb NHCOCHa V = /
ocn ocn
/j~4< / j ~ 4 <
P V -® P V -®
cha w ocha /r~£ s^t hg cha w ocha / r ~ £ s ^ t hg
çk«, -o çk «, -o
NHCOCH, NHCOCH,
(CH30)2S02 (CH30) 2S02
(CH30)2S02 (CH30) 2S02
(CH30)2S02 (CH30) 2S02
Rot red
Rot blaust. Rot Red bluish. red
622 622
623 623
624 624
hac-chj H. C CH. hac-chj H. C CH.
VC VC
ni>k nhg ni> k nhg
Ih hapfh, nc^chg ha o< Ih hapfh, nc ^ chg ha o <
/C2 H# / C2 H #
cha-0 cha-0
chj -^3 chj - ^ 3
o-<c:$ o- <c: $
_ /h) _ /H)
€Kch,.q> € Kch, .q>
(CH3o)2so2 (CH3o) 2so2
(CH3o)2so2 (CH3o) 2so2
(CH30)2S02 (CH30) 2S02
Orange orange
Orange orange
Orange orange
625 625
626 626
627 627
✓ ca hg ✓ approx
\=/ ^chgchg-^^ \ = / ^ chgchg - ^^
/—\ .CHaO / - \ .CHaO
ci ci
6469/73 6469/73
(CH30)2S02 (CH30) 2S02
(CH30)2S02 (CH30) 2S02
(CH30)2S02 (CH30) 2S02
Orange orange
Orange orange
Orange orange
143 144 143 144
Beispiel Diazokomponente Kupplungskomponente Quaternierungsmittel Farbton auf Example diazo component coupling component quaternizing agent color
Polyacrylnitril h, p-ch,, Polyacrylonitrile h, p-ch ,,
HaC 'CH, HaC 'CH,
v~( /-\ / cj h, v ~ (/ - \ / cj h,
628 n^j^-nha v_y"n\ (CH30)2S02 gelbst. Rot i-w ch" "w h, c^ cha 628 n ^ j ^ -nha v_y "n \ (CH30) 2S02 yellow. Red i-w ch" "w h, c ^ cha
.chachjcn .chachjcn
629 „ V-N (CH30)2S02 gelbst. Rot 629 „V-N (CH30) 2S02 yellow. red
630 630
rv0h,"q rv0h, "q
>=^ vcha-^^ > = ^ vcha - ^^
(CH30)2S02 (CH30) 2S02
gelbst. Rot yellow. red
C H C H
631 „ (/ NVjf' * 1 /—v (CH30)2S02 gelbst. Rot 631 „(/ NVjf '* 1 / —v (CH30) 2S02 yellow. Red
PQch,<3 PQch, <3
chs w chs w
'Ci Hf 'Ci Hf
632 „ F *>N i—\ (CH30)2S02 Rot 632 "F *> N i— \ (CH30) 2S02 red
jT"\ ns jT "\ ns
P"c*-© P "c * - ©
NHCOCHg NHCOCHg
ç% ç%
633 „ N- >rTV (CH30)2S02 Rot 633 „N-> rTV (CH30) 2S02 red
CHb rC** CHb rC **
OCHg OCHg
/rC 'C»H« / rC 'C "H"
634 „ (' xvn /—v (CH30)2S02 blaust. Rot 634 "('xvn / -v (CH30) 2S02 bluish red
-ch. -C 7 NHCOCHg -ch. -C 7 NHCOCHg
* /cahg * / cahg
, "* €kch, o , "* € kch, o
0 0
635 ÌKjy-Wk (' NhN WK VSXODIi gelbst.Rot 635 ÌKjy-Wk ('NhN WK VSXODIi yellow.red
6469/73 6469/73
Beisi Beisi
636 636
637 637
638 638
639 639
640 640
641 641
642 642
643 643
644 644
145 145
146 146
Diazokomponente Kupplungskomponente Quaternierungsmittel Diazo component coupling component quaternizing agent
M M
OK™" 5% hfo^ock, OK ™ "5% hfo ^ ock,
XÎ) XÎ)
CH CH
/r^ "CH® / r ^ "CH®
/r\ 'c*hb / r \ 'c * hb
P"v-o cha w exCHsC^N P "v-o cha w exCHsC ^ N
fvc*1R fvc * 1R
,r nch«0 , r nch «0
O-n'1 O-n'1
y=j N y = j N
'c.h. 'c.h.
cn '"w© cn '"w ©
6469/73 6469/73
147 147
148 148
Beispiel Diazokomponente Kupplungskomponente Example diazo component coupling component
Quaternierungsmittel Quaternizing agent
Farbton auf Polyacrylnitril Color on polyacrylonitrile
645 645
Ò O
646 646
NHCOCHg sch»"0 NHCOCHg sh »" 0
OC Hg OC ed
/nL 'CaH» / nL 'CaH »
p\*.r cha blaust. Rot p \ *. r cha bluish. red
Rot red
647 647
_>pci^ch2ch3 _> pci ^ ch2ch3
/ 2 / 2nd
vch^ vch ^
nhcoch, nhcoch,
blaust. Rot bluish. red
648 <NV> NHa 648 <NV> NHa
£ £
z > / C» H z> / C »H
©V ' © V '
ch.o ch.o
(CH30)2S02 Orange (CH30) 2S02 orange
649 649
<r\/ch= -Q <r \ / ch = -Q
vcha vcha
(CH30)2S02 Orange (CH30) 2S02 orange
650 650
XÜ> XÜ>
0n.cha-©> 0n.cha- ©>
(CH30)2S02 Orange (CH30) 2S02 orange
651 651
jT-\ sca h. jT- \ sca h.
\=>~ch,CH,-Q \ => ~ ch, CH, -Q
(CH30)2S02 Orange (CH30) 2S02 orange
652 652
ncnch,-^) ncnch, - ^)
(CH30)2S02 Orange (CH30) 2S02 orange
6469/73 6469/73
149 149
150 150
Beispiel Diazokomponente Example diazo component
Kupplungskomponente Coupling component
Quaternierungsmittel Quaternizing agent
Farbton auf Polyacrylnitril Color on polyacrylonitrile
653 653
(CH30)2S02 (CH30) 2S02
Orange orange
C H C H
654 „ \V-N' 8 * _ (CH30)2S02 Orange cha 654 „\ V-N '8 * _ (CH30) 2S02 Orange cha
/t7\ -ch2 "©> / t7 \ -ch2 "©>
655 „ N\Cj^ (CH30)2S02 gelbst. Rot 655 "N \ Cj ^ (CH30) 2S02 yellow. red
CHg y—. yCtHa CHg y—. yCtHa
656 „ ^ y-N >5""vV (CH30)2S02 gelbst. Rot vch2 chj -p n) 656 "^ y-N> 5" "vV (CH30) 2S02 yellow. Red vch2 chj -p n)
CH,, W CH ,, W
'cahe 'cahe
657 „ <(_y-N (CH30)2S02 Rot ncha 657 „<(_ y-N (CH30) 2S02 red ncha
NHCOCHa NHCOCHa
OC Hg c -c' OC Hg c -c '
658 „ K_/Ns /r\ (CH30)2S02 Rot cha ocha ^cth8 658 „K_ / Ns / r \ (CH30) 2S02 red cha ocha ^ cth8
✓ç.h. ✓ç.h.
ocha ok
659 „ \/"N' " "/"TV (CH30)2S02 blaust. Rot 659 "\ /" N '"" / "TV (CH30) 2S02 bluish. red
■•cn-o ■ • cn-o
NHCOCHa N—7 NHCOCHa N-7
6469/73 6469/73
151 151
152 152
Beispiel Diazokomponente Kupplungskomponente Ouaternierungsmittel Farbton auf Example Diazo component Coupling component Ouaternierungsmittel color
Polyacrylnitril f v. i a /CHj CHji CN Polyacrylonitrile f v. i a / CHj CHji CN
660 f \>n (ch3o)2so2 Rot 660 f \> n (ch3o) 2so2 red
<3 <3
Cl Cl
662 662
2 1 2 1
661 n^^-nhg c=)"n\ * ch2=ch-cn Rot 661 n ^^ - nhg c =) "n \ * ch2 = ch-cn red
ch,=ch-cn Rot ch, = ch-cn red
/© / ©
663 „ /^S-N CH.-CH-CN Rot 663 "/ ^ S-N CH.-CH-CN Red
© ©
0 0
Cl a/Ct Hg vch,-Q Cl a / Ct Hg vch, -Q
fw 2 5 ^ fw 2 5 ^
y=f "^chgcha \J) y = f "^ chgcha \ J)
ch3 ch3
^ 'CH» ^ 'CH »
w^cn^ci pv'-© w ^ cn ^ ci pv'- ©
gha gha
Rot red
664 tf VnH2 O-n'0*"'.. yT*v CH..CH-CN ch, 664 tf VnH2 O-n'0 * "'.. yT * v CH..CH-CN ch,
,c2hc , c2hc
665 „ (/ \>tf rtv ch2=ch-cn Rot 665 „(/ \> tf rtv ch2 = ch-cn red
666 N^T-NHa (__N>Nv /T~Z\. ch2=ch-cn Rot 666 N ^ T-NHa (__N> Nv / T ~ Z \. Ch2 = ch-cn red
✓ C, H, ✓ C, H,
667 „ (' n)"n. ch2=ch-cn blaust. Rot 667 "('n)" n. Ch2 = ch-cn bluish. Red
668 668
/CHj CHjCN / CHj CHjCN
P" V <3 P "V <3
ch,» ^ ch, »^
6469/73 6469/73
ch2=ch-cn blaust. Rot ch2 = ch-cn bluish. red
Beisf Example
669 669
670 670
671 671
672 672
673 673
674 674
675 675
676 676
153 153
154 154
Diazokomponente Diazo component
Kupplungskomponente Coupling component
Quaternierungsmittel h Quaternizing agent h
'7~ v n^nks '7 ~ v n ^ nks
/ta /ch,-© / ta / ch, - ©
Ç^ck> -© Ç ^ ck> - ©
ch2=ch-cn ch2 = ch-cn
Cl Cl
^c2 h8 ^ c2 h8
y=^ ^chacha-o on w ch2=ch-cn y = ^ ^ chacha-o on w ch2 = ch-cn
/T\ 'c2h5 / T \ 'c2h5
nhcochg ch,=ch-cn nhcochg ch, = ch-cn
//^-n cha ocha /c. // ^ - n cha ocha / c.
ncn-<© ncn- <©
/c2h8 / c2h8
ch2=ch-cn ch2 = ch-cn
,0ch3 , 0ch3
// \\ 'C*H» // \\ 'C * H »
a \\-n v nch2"0 a \\ - n v nch2 "0
*u Vr=y v=-y * u Vr = y v = -y
N HC oc h, N HC oc h,
ch2=ch-cn n^^nha h ch2 = ch-cn n ^^ nha h
^ / chg chg cn ch, w ^ / chg chg cn ch, w
(ch30)2s02 (ch30) 2s02
CX CX
c2h3 c2h3
en-© en- ©
(ch30)2s02 (ch30) 2s02
,c, h* , c, h *
(ch30)2s02 (ch30) 2s02
2 5 ^ 2 5 ^
nchj chj nchj chj
6469/73 6469/73
155 155
156 156
Beispiel Diazokomponente Kupplungskomponente Example diazo component coupling component
Quaternierungsmittel Quaternizing agent
Farbton auf Polyacrylnitril Color on polyacrylonitrile
677 677
h chj w h chj w
(ch30)2s02 (ch30) 2s02
gelbst. Rot yellow. red
678 678
CKh,^ CKh, ^
(ch30)2s02 (ch30) 2s02
rotst. Orange red orange
679 679
>=/ scha > = / scha
(ch30)2s02 (ch30) 2s02
gelbst. Rot yellow. red
680 680
681 681
cha x-/ cha x- /
(ch30)2s02 (ch30) 2s02
(ch30)2s02 (ch30) 2s02
Rot red
Rot red
682. 682.
/chgcnoh / chgcnoh
(ch30)2s02 (ch30) 2s02
Orange orange
683 683
p""' p "" '
ths ch, cha 0h sch,h© ths ch, cha 0h sh, h ©
(ch30)2s02 (ch30) 2s02
Rot red
6469/73 6469/73
157 157
158 158
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US70490976A | 1976-07-14 | 1976-07-14 | |
US05/771,286 US4089969A (en) | 1976-07-14 | 1977-02-23 | 5-Aroyl-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acid derivatives and process for the production thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
CH646973A5 true CH646973A5 (en) | 1984-12-28 |
Family
ID=27107410
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH850077A CH641458A5 (en) | 1976-07-14 | 1977-07-08 | Process for preparing 5-aroyl-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acid esters |
CH86684A CH646973A5 (en) | 1976-07-14 | 1984-02-22 | Process for the preparation of novel 5-aroyl-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acids |
CH86584A CH646972A5 (en) | 1976-07-14 | 1984-02-22 | Process for the preparation of new 5-aroyl-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acids |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH850077A CH641458A5 (en) | 1976-07-14 | 1977-07-08 | Process for preparing 5-aroyl-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acid esters |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH86584A CH646972A5 (en) | 1976-07-14 | 1984-02-22 | Process for the preparation of new 5-aroyl-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acids |
Country Status (27)
Country | Link |
---|---|
JP (1) | JPS539788A (en) |
AR (1) | AR224997A1 (en) |
CA (1) | CA1102809A (en) |
CH (3) | CH641458A5 (en) |
CS (1) | CS204954B2 (en) |
DE (2) | DE2731678A1 (en) |
DK (1) | DK151886C (en) |
ES (2) | ES460706A1 (en) |
FI (1) | FI63406C (en) |
FR (2) | FR2358406A1 (en) |
GB (1) | GB1554075A (en) |
GR (1) | GR61111B (en) |
HK (1) | HK15981A (en) |
HU (1) | HU174224B (en) |
IE (1) | IE45253B1 (en) |
IL (2) | IL52493A (en) |
IT (1) | IT1117313B (en) |
MX (1) | MX163202B (en) |
MY (1) | MY8100357A (en) |
NL (2) | NL186318C (en) |
NO (1) | NO147564C (en) |
NZ (1) | NZ184610A (en) |
PL (4) | PL124711B1 (en) |
PT (1) | PT66780B (en) |
SE (1) | SE434643B (en) |
SU (1) | SU695558A3 (en) |
YU (1) | YU40816B (en) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4140698A (en) * | 1977-07-25 | 1979-02-20 | Syntex (Usa) Inc. | 1,2-Dihydro-3H-pyrrolo[1,2-a]pyrrole-1-nitriles |
JPS55124633A (en) * | 1979-03-19 | 1980-09-25 | Sohachi Takeuchi | Manufacturing method of tubular vessel |
US4344943A (en) * | 1980-06-09 | 1982-08-17 | Syntex (U.S.A.) Inc. | 6-Chloro- or 6-bromo-1,2-dihydro-3H-pyrrolo[1,2-a]-pyrrole-1-carboxylic acids and derivatives thereof |
US4353829A (en) * | 1980-11-21 | 1982-10-12 | Syntex (U.S.A.) Inc. | Process for 5-aroylation of 1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic esters |
JPS5910589A (en) * | 1982-06-10 | 1984-01-20 | メルク エンド カムパニー インコーポレーテツド | Antiinflammatory and analgesic novel 5-(pyrrol-2-oyl)-1,2-dihydro-3h-pyrrolo(1,2-a) pyrrole derivative |
US4511724A (en) * | 1982-06-10 | 1985-04-16 | Merck & Co., Inc. | 5-(Pyrrol-2-oyl)-1,2-dihydro-3H-pyrrolo [1,2-a]pyrrole derivatives as anti-inflammatory and analgesic agents |
US4874871A (en) * | 1987-03-25 | 1989-10-17 | Syntex (U.S.A.) Inc. | Process for preparing (+)-2,3-Dihydro-1H-pyrrolo[1,2-a]pyrrole-1-carboxylic acid and related compounds |
JPH0739418B2 (en) * | 1987-09-10 | 1995-05-01 | 久光製薬株式会社 | Novel 3-aroyl-6,7-dihydro-5H-pyrrolo [1,2-c] imidazole-7-carboxylic acid derivative |
JP2649168B2 (en) * | 1988-02-25 | 1997-09-03 | 久光製薬株式会社 | Novel 5,6-diphenyl-1,2-dihydro-3H-pyrrolo [1,2-a] pyrrole-1-carboxylic acid derivatives |
IT1250691B (en) * | 1991-07-22 | 1995-04-21 | Giancarlo Santus | THERAPEUTIC COMPOSITIONS FOR INTRANASAL ADMINISTRATION INCLUDING KETOROLAC. |
DE69229506T2 (en) * | 1991-11-11 | 1999-10-28 | Hisamitsu Pharmaceutical Co., Inc. | WARM ENVELOPE CONTAINING KETOROLAC |
DE4300697C1 (en) * | 1993-01-13 | 1994-05-19 | Roemmers Sa | New 2-pyrrolidino-ethyl ester of ketorolac - useful as analgesic, antiinflammatory and antipyretic agent with low ulcerogenicity |
US5622948A (en) * | 1994-12-01 | 1997-04-22 | Syntex (U.S.A.) Inc. | Pyrrole pyridazine and pyridazinone anti-inflammatory agents |
JP2008210666A (en) * | 2007-02-27 | 2008-09-11 | Okamura Corp | Lighting system in merchandise display shelf |
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1977
- 1977-05-17 JP JP5697777A patent/JPS539788A/en active Granted
- 1977-07-07 AR AR268356A patent/AR224997A1/en active
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- 1977-07-11 YU YU1721/77A patent/YU40816B/en unknown
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- 1977-07-11 FR FR7721356A patent/FR2358406A1/en active Granted
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- 1977-07-13 ES ES460706A patent/ES460706A1/en not_active Expired
- 1977-07-13 SU SU772501050A patent/SU695558A3/en active
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- 1977-07-13 DE DE2760330A patent/DE2760330C2/de not_active Expired
- 1977-07-13 PL PL1977227290A patent/PL124444B1/en unknown
- 1977-07-13 PL PL1977227291A patent/PL124445B1/en unknown
- 1977-07-13 IT IT68630/77A patent/IT1117313B/en active Protection Beyond IP Right Term
- 1977-07-13 PL PL1977199603A patent/PL109390B1/en unknown
- 1977-07-14 HU HU77SI1582A patent/HU174224B/en unknown
- 1977-12-20 FR FR7738508A patent/FR2375234A1/en active Granted
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1978
- 1978-05-24 ES ES470214A patent/ES470214A1/en not_active Expired
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1979
- 1979-11-22 IL IL58779A patent/IL58779A0/en unknown
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1981
- 1981-04-23 HK HK159/81A patent/HK15981A/en unknown
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1984
- 1984-02-22 CH CH86684A patent/CH646973A5/en not_active IP Right Cessation
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1991
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1993
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