http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-1185970-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D295-096
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D275-06
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D295-096
filingDate 1982-12-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1985-04-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b442a184be09d3702b1465e218fe0e34
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_409f1914fd481091f05399e8c8878ed4
publicationDate 1985-04-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-1185970-A
titleOfInvention Benzo-fused heterocyclic anti-ulcer agents
abstract ABSTRACT OF THE DISCLOSURE Compounds having the formula: wherein R is hydrogen, mono- or dihalo, amino, nitro, cyano, hydroxy, trifluoromethyl, mercapto, lower alkyl, lower alkoxy, alkanoyl, lowercycloalkyl carboxy, alkoxycarbonyl, mono- or di-lower alkyl substituted amino, alkanoylamino, lower alkyl thio, loweralkylsulfonyl, sulfamoyl, lower alkyl substituted sulfumoyl, phenyl or phenyl substituted with halo, lower alkyl, lower alkoxy, trifluoromethyl, hydroxy, amino, cyano or nitro; X is SO2, SO, S or C=O; and A is an amine selected from the group: wherein R1 is hydrogen or R2CH2 wherein R2 is mono- or dilower-alkylamino, mono- or di-N-lower alkylaminolower-alkyl, (2-furyl)methylamino, benzylamino, lowercycloalkylamino, 1-pyrroli-dinyl, 1-piperidinyl, 1-hexahydroazepinyl, 1-octahydroazocinyl, 3-thiazolidinyl, 4-morpholinyl or 4-thiomorpholinyl; R3 is hydrogen or (1-piperidinyl)methyl with the proviso that when R3 is (1-piperidinyl)methyl, R1 is hydrogen; n is 1 to 4, and the pharmacologically acceptable salts thereof, have a selective action on H2 histamine receptors and which inhibit gastric acid secretion.
priorityDate 1981-12-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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