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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D243-38
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P1-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D243-38
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-55
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P1-04
filingDate 1981-07-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1983-10-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bf9eeae10ec5e2171482990b3cd2d25f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_17a71176cc02f70436fd7ae1c61d0a72
publicationDate 1983-10-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-1154763-A
titleOfInvention In 5-position substituted 5,10-dihydro-11h- dibenzo[b,e][1,4] diazepine-11-ones, processes for their preparation, and pharmaceutical compositions containing these compounds
abstract ABSTRACT 5,10-Dihydro 1 H-beno [b,e][1,4]diazepine-11-ones Compounds of general formula I, , (I) wherein R1 represents a hydrogen atom or a methyl or ethyl group; R2 represents a hydrogen or chlorine atom; R3 represents a hydrogen or chlorine atom; and R4 represents a pyrrolidino, piperidino, 2-methyl-piperidino, 2-ethyl-piperidino, 2,6-dimethylpiperidino or morpholino.group: and acid addition salts thereof of use as ulcer-inhibiting and secretion-inhibiting agents.
priorityDate 1980-07-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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