http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CH-674988-A5

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09B29-0059
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09B29-3686
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09B29-3643
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B29-36
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B29-44
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B29-00
filingDate 1988-02-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_217c2eaf39bfad15e616800b4f28d67d
publicationDate 1990-08-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CH-674988-A5
titleOfInvention New azo dyestuff used esp. for dyeing polyamide
abstract New azo dyestuffs are 5-cyclohexoyl-thiophene (2-azo-6) 1,2,3,4-tetrahydroquinoline or (2-azo-7) 3,4-dihydro-2H-1,4-benzoxazine cpds. of formula (I). In (I), R1 = H or (substd.) 1-10C alkyl; R2 = -CN, -CON(R8)R9, -COR10, -COOR11, -SO2R12 or -CONHNR13; R3 = H, halogen, 1-4C alkyl, 2-4C alkyl, 2-6C alkanoylamino, 1-10C alkoxy or phenoxy; R4 = (substd.) 1-10C alkyl; R5 = 1-4C alkyl; R6 = H or 1-4C alkyl; R7 = H or 1-4C alkyl; R8, R9 and R13 independently = H, or (substd.) 1-10C alkyl, 5-7C cycloalkyl, phenyl or naphthyl; R10, R11 and R12 = (substd.) 1-10C alkyl, 5-7C cycloalkyl, phenyl, or naphthyl; X = O or -CH(R14)-; R14 = H or 1-4C alkyl; Y = a gp. imparting solubility in water; n and m independently = 1 or 2. (I) are prepd. by diazotising the corresp. 2-aminothiophene (II) (with 0-1 Y substit.), coupling with the tetrahydro-quinoline or -benzoxazine cpd. (III) (with 0-1 Y substit.) and introducing 1 or 2 Y gps. if necessary. The prepn. of (II) (not claimed) is described in the text. (III) are known cpds. or can be prepd. by conventional methods.
priorityDate 1988-02-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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