http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0183369-A2

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filingDate 1985-10-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e874256c5d765276af5be0a1df6ed628
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a05a8e6e2e8d543d85839404e06de7d8
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publicationDate 1986-06-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0183369-A2
titleOfInvention Dihydroisoquinoline derivatives, process for their preparation and pharmaceutical compositions containing them
abstract Compounds of the general formula In nin which:n R, and R 2 are independently hydrogen, C, 6 alkyl ortogether are a group X which is C 3 6 polymethylene optionally in which one carbon atom is replaced by O, S or NR 6 wherein R 6 is hydrogen or C 1 6 alkyl; R 3 is a mono- or fused bi-cyclic heteroaromatic group having up to ten atoms in the aromatic ring(s), not more than four of which are selected from nitrogen, oxygen or sulphur, optionally C-substituted by one or more substituents selected from halogen, CF 3 , nitro, C 1-6 alkoxy, C 1-6 alkylthio, C 2-7 alkanoyl or cyano; or is phenyl or naphthyl, optionally substituted by one or more substituents selected from halogen, CF 3 , nitro, C 1-6 alkyl, C 1 6 alkoxy, C 1 6 alkylthio, C 2-7 alkanoyl, carboxyl, C 1-6 alkoxycarbonyl, cyano, CONR 7 R 8 wherein R 7 and R 8 are selected from hydrogen or C 1-6 alkyl or together are a group X; NR 9 R 10 wherein R 9 and R 10 are selected from hydrogen, C 1-6 alkyl, C 2 - 7 alkanoyl or C 1-6 alkylsulphonyl or together are a group X; SO 2 NR 11 R 12 wherein R 11 and R 12 are selected from hydrogen or C 1-6 alkyl or together are a group X; or S(O) m R 13 wherein m is 1 or 2 and R 13 is C 1-6 alkyl; Z is naphthyl or a mono- or fused bycyclic heteroaromatic ring having up to ten atoms in the aromatic ring(s), not more than four of which are selected from nitrogen, oxygen or sulphur or (when R 3 is an optionally substituted naphthyl or heteroaromatic group as defined) Z is a phyenyl ring; and Z is optionally C-substituted by one or two substituents R 4 and R 5 which are independently selected from C 1-6 alkyl, cyano, amino, aminocarbonyl or aminocarbamoyl optionally substituted by one or two C 1-6 alkyl groups or by a group X, halogen, CF 3 , nitro, C 1-6 alkoxy, C 1-6 alkylthio, C 2-7 alkanoyloxy or hydroxy, or together on adjacent carbon atoms are methylenedioxy or C 3-5 polymethylene, are disclosed as an active therapeutic substances for the treatment of inflammatory conditions.
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priorityDate 1984-10-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 531.