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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c902faf6ae746c51fc8010672fc22894
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D487-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-04
filingDate 1969-02-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1971-03-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3d607a323f4fa14d0adfeea4da4076e1
publicationDate 1971-03-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-3573322-A
titleOfInvention Polyhydroazepino(2,3-b) indoles
abstract NEW POLYHYDROAZEPINO(2,3-B)INDOLES OF THE FORMULA XIV: 1-R1,5A-R2-1,2,3,4,5,5A-HEXAHYDROAZEPINO(2,3-B)INDOLE WHEREIN R1 IS SELECTED FROM THE GROUP CONSISTING OF HYDROGEN, ETHYL AND ACETYL AND WHEREIN R2 IS SELECTED FROM THE GROUP CONSISTING OF HYDROGEN, HYDROXY AND ACETOXY WITH THE PROVISO THAT R2 IS ACETOXY ONLY IF R1 IS HYDROGEN OR ACETYL, ARE PREPARED. THESE COMPOUNDS AND THEIR PHARMACOLOGICALLY ACCEPTABLE ACID ADDITION SALTS HAVE SEDATIVE ACTION AND CAN BE USED IN MAMMALS AND BIRDS AS TRANQUILIZERS.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4545935-A
priorityDate 1969-02-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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