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Outgoing Links

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D243-12
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D243-12
filingDate 1971-10-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1975-01-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fdbc00857b2425017d3d5d9407a74fd1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_41490faa1b418157a08650615602560e
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_15d939ccea8e5fb41ed4485c8295c8af
publicationDate 1975-01-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-3862136-A
titleOfInvention 2-halo-5-phenyl-4h-3,5-dihydro-1,5-benzodiazepin-4-ones and salts thereof
abstract Compounds of the formula WHEREIN R1 and R2, which may be identical to or different from each other, are each hydrogen, straight or branched alkyl of 1 to 4 carbon atoms, di-lower alkylamino-(alkyl of 1 to 4 carbon atoms), hydroxy-(alkyl of 1 to 4 carbon atoms), alkenyl of 2 to 4 carbon atoms or, together with each other and the nitrogen atom to which they are attached, form a 6-membered saturated heterocyclic ring which may optionally have a methyl or tolyl substituent attached thereto, R3 is phenyl, o-halo-phenyl, o-nitro-phenyl or otrifluoromethyl-phenyl, and R4 is halogen, nitro or trifluoromethyl, AND NON-TOXIC, PHARMACOLOGICALLY ACCEPTABLE ACID ADDITION SALTS THEREOF; THE COMPOUNDS AS WELL AS THEIR SALTS ARE USEFUL AS TRANQUILIZERS.
priorityDate 1970-11-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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