Predicate |
Object |
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 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9399642-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-10906912-B2 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 |