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1. WO1996006137 - NAPHTHOLACTAM DYES

Publication Number WO/1996/006137
Publication Date 29.02.1996
International Application No. PCT/EP1995/003112
International Filing Date 04.08.1995
Chapter 2 Demand Filed 29.11.1995
IPC
C07D 401/04 2006.01
CCHEMISTRY; METALLURGY
07ORGANIC CHEMISTRY
DHETEROCYCLIC COMPOUNDS
401Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
02containing two hetero rings
04directly linked by a ring-member-to-ring- member bond
C07D 495/06 2006.01
CCHEMISTRY; METALLURGY
07ORGANIC CHEMISTRY
DHETEROCYCLIC COMPOUNDS
495Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
02in which the condensed system contains two hetero rings
06Peri-condensed systems
C09B 57/06 2006.01
CCHEMISTRY; METALLURGY
09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES; MORDANTS; LAKES
57Other synthetic dyes of known constitution
06Naphtholactam dyes
CPC
C07D 401/04
CCHEMISTRY; METALLURGY
07ORGANIC CHEMISTRY
DHETEROCYCLIC COMPOUNDS
401Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
02containing two hetero rings
04directly linked by a ring-member-to-ring-member bond
C07D 495/06
CCHEMISTRY; METALLURGY
07ORGANIC CHEMISTRY
DHETEROCYCLIC COMPOUNDS
495Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
02in which the condensed system contains two hetero rings
06Peri-condensed systems
C09B 57/06
CCHEMISTRY; METALLURGY
09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES ; , e.g. PIGMENTS; MORDANTS; LAKES
57Other synthetic dyes of known constitution
06Naphtholactam dyes
Applicants
  • BASF AKTIENGESELLSCHAFT [DE/DE]; D-67056 Ludwigshafen, DE (AllExceptUS)
  • GRUND, Clemens [DE/DE]; DE (UsOnly)
  • SCHEFCZIK, Ernst [DE/DE]; DE (UsOnly)
  • LAMM, Gunther [DE/DE]; DE (UsOnly)
  • MERGER, Roland [DE/DE]; DE (UsOnly)
  • SENS, Rüdiger [DE/DE]; DE (UsOnly)
Inventors
  • GRUND, Clemens; DE
  • SCHEFCZIK, Ernst; DE
  • LAMM, Gunther; DE
  • MERGER, Roland; DE
  • SENS, Rüdiger; DE
Common Representative
  • BASF AKTIENGESELLSCHAFT; D-67056 Ludwigshafen, DE
Priority Data
P 44 29 548.019.08.1994DE
Publication Language German (DE)
Filing Language German (DE)
Designated States
Title
(DE) NAPHTHOLACTAMFARBSTOFFE
(EN) NAPHTHOLACTAM DYES
(FR) COLORANTS DE NAPHTOLACTAME
Abstract
(DE)
Naphtholactamderivate der Formel (I), in der R1 Wasserstoff, gegebenenfalls substituiertes C1-C6-Alkyl, C5-C7-Cycloalkyl oder gegebenenfalls substituiertes Phenyl, R2 und R3 Wasserstoff, C1-C8-Alkanoyl, gegebenenfalls substituiertes Benzoyl, gegebenenfalls substituiertes C2-C4-Alkyl, gegebenenfalls substituiertes C2-C4-Alkenyl, gegebenenfalls substituiertes C2-C4-Alkinyl, Halogen, Nitro, Sulfamoyl, gegebenenfalls substituiertes Hydroxy, gegebenenfalls substituiertes Mercapto, C1-C6-Alkylsulfonyl oder gegebenenfalls substituiertes Phenylsulfonyl, R4 Wasserstoff oder zusammen mit R3 einen Rest der Formel (II), R5 Wasserstoff oder C1-C6-Alkyl, R6 Cyano, Carbamoyl, C1-C4-Mono- oder Dialkylcarbamoyl, Carboxyl oder C1-C4-Alkoxycarbonyl und R7 substituiertes C1-C4-Alkyl, gegebenenfalls substituiertes C5-C13-Alkyl oder Benzoyl bedeuten, sowie deren Verwendung zum Färben oder Bedrucken von textilen Materialien.
(EN)
The invention concerns naphtholactam derivatives of formula (I), in which: R1 represents hydrogen, optionally substituted C1-C6 alkyl, C5-C6 cycloalkyl or substituted phenyl; R2 and R3 represent hydrogen, C1-C8 alkanoyl, optionally substituted benzoyl, optionally substituted C2-C4 alkyl, optionally substituted C2-C4 alkenyl, optionally substituted C2-C4 alkinyl, a halogen, nitro, sulphamoyl, optionally substituted hydroxy, optionally substituted mercapto, C1-C6 alkylsulphonyl or optionally substituted phenylsulphonyl; R4 represents hydrogen or, with R3, a group of formula (II); R5 represents hydrogen or C1-C6 alkyl; R6 represents cyano, carbamoyl, C1-C4 mono- or dialkylcarbamoyl, carboxyl or C1-C4 alkoxycarbonyl; and R7 represents substituted C1-C4 alkyl, optionally substituted C5-C13 alkyl or benzoyl. Also disclosed is the use of these derivatives for dyeing or printing textiles.
(FR)
L'invention concerne des dérivés de naphtolactame de formule (I) où R1 représente hydrogène, alkyle C1-C6 éventuellement substitué, cycloalkyle C5-C7 ou phényle éventuellement substitué; R2 et R3 représentent hydrogène, alcanoyle C1-C8, benzoyle éventuellement substitué, alkyle C2-C4 éventuellement substitué, alcényle C2-C4 éventuellement substitué, alcinyle C2-C4 éventuellement substitué, halogène, nitro, sulfamoyle, hydroxy éventuellement substitué, mercapto éventuellement substitué, alkylsulfonyle C1-C6 ou phénylsulfonyle éventuellement substitué; R4 représente hydrogène ou, conjointement avec R3, un radical de formule (II); R5 représente hydrogène ou alkyle C1-C6; R6 représente cyano, carbamoyle, mono ou dialkylcarbamoyle C1-C4, carboxyle ou alcoxycarbonyle C1-C4 et R7 représente alkyle C1-C4 substitué, alkyle C5-C13 éventuellement substitué ou benzoyle. L'invention concerne également l'utilisation de ces dérivés pour la teinture ou l'impression de matériaux textiles.
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