http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0092698-A1

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filingDate 1983-04-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7120f8390d189ccb3d7a23fd85d3fe05
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7b156a401b38ac4677edbb054ca6032f
publicationDate 1983-11-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0092698-A1
titleOfInvention Process for the preparation of cationic methine dyes
abstract R für gegebenenfalls substituiertes Alkyl, R' für Wasserstoff, Alkyl, Halogen, Alkoxy, Hydroxyalkoxy, gegebenenfalls substituiertes Phenoxy, Benzyloxy- oder Benzyl, Carboxyl, Carbonsäurealkylester, eine gegebenenfalls substituierte Carbonamidgruppe oder Sulfonamidgruppe, Alkylsulfonyl, Phenylsulfonyl, Cyan, Trifluormethyl, Acetyl oder Benzoyl, A fürn worin R 2 und R 3 für gegebenenfalls substituiertes Alkyl stehen, R 2 zusätzlich für substituiertes Phenyl oder Benzyl steht, oder mit dem benachbarten C-Atom des Benzolringes einen 5- oder 6-Ring bildet, R 4 Wasserstoff, Alkyl, Alkoxy oder Halogen bedeutet, oder fürn worin R 5 für Alkyl, gegebenenfalls substituiertes Phenyl oder Carbalkoxy, R 6 für Wasserstoff, gegebenenfalls substituiertes Alkyl, R 7 für Wasserstoff, Halogen, Alkoxy, Carbalkoxy, Alkylsulfonyl, Phenylsulfonyl, Acetyl oder Benzoyl stehen, oder fürn worin R 8 bzw. R 9 die gleiche Bedeutung wie R bzw. R 1 haben, X Aryl, Alkyl oder Alkoxy und m, n, o und p 1 bis 4 bedeuten, erfolgt durch Kondensation vonn mit 1 - 7 Mol X SO 3 H oder vonn mit 0 - 6 Mol X S0 3 H und mit einer Verbindungn in Gegenwart vou 0 · 30 Gew. % eines organischen Lösungsmittels und von 0 - 15 Gew % Wasser. The production of cationic methine dyes of the formula in which R represents optionally substituted alkyl, R 'represents hydrogen, alkyl, halogen, alkoxy, hydroxyalkoxy, optionally substituted phenoxy, benzyloxy or benzyl, carboxyl, alkyl carboxylate, an optionally substituted carbonamide group or sulfonamide group, alkylsulfonyl, phenylsulfonyl, cyano, trifluoromethyl, acetyl or benzoyl, A for wherein R 2 and R 3 represent optionally substituted alkyl, R 2 additionally represents substituted phenyl or benzyl, or forms a 5- or 6-ring with the adjacent carbon atom of the benzene ring, R 4 represents hydrogen, alkyl, alkoxy or halogen, or for wherein R 5 represents alkyl, optionally substituted phenyl or carbalkoxy, R 6 represents hydrogen, optionally substituted alkyl, R 7 stands for hydrogen, halogen, alkoxy, carbalkoxy, alkylsulfonyl, phenylsulfonyl, acetyl or benzoyl, or for wherein R 8 and R 9 have the same meaning as R and R 1 , X aryl, alkyl or alkoxy and m, n, o and p represent 1 to 4, takes place by condensation of with 1 - 7 mol X SO 3 H or from with 0 - 6 mol X S0 3 H and with one compound in the presence of 0 · 30% by weight of an organic solvent and 0 - 15% by weight of water.
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priorityDate 1982-04-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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