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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e4155c237ba921600e5d9125cf2f6a2d
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D487-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D487-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-04
filingDate 1982-09-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1984-01-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_166ab6a6bc64bf12c269bbd5fa38a9b2
publicationDate 1984-01-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4428880-A
titleOfInvention Azepino[4,5-d]indole derivatives and preparation thereof
abstract This invention relates to novel tetrahydroazepinoindoles used in the preparation of novel alkyl pyrrolo(2,3-d)carbazole-6-carboxylates and to addition salts thereof; and to preparation of the same by a synthesis sequence starting from a tryptamine and a 3-halopyruvate and involving a rearrangement of the reaction mixture, said rearrangement being effected by heating the reaction mixture in the presence of a base. The pyrrolo(2,3-d)carbazole final products have both antianoxic and psychotropic activities.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9399643-B2
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-D826893-S
priorityDate 1981-05-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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