http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4628100-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_f88f84fc279fe5d0b9b5ec3c88c2e2b2
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-74
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-74
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04
filingDate 1985-06-26^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1986-12-09^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_322feee405794c458c99fb427506077b
publicationDate 1986-12-09^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4628100-A
titleOfInvention Intermediates for the preparation of aryl substituted pyrido[1,4]benzodiazepines
abstract Intermediates for preparing pyrido [1,4] benzodiazepines having antidepressant activity are disclosed of the formula <IMAGE> wherein, R is hydrogen, loweralkyl, -alk1-NR1R2, -alk1-N=CH-OC2H5 or <IMAGE> R1 and R2 are loweralkyl, -C(O)-O-loweralkyl or R1 and R2 taken together with the adjacent nitrogen atom may form a 1-piperidinyl, 1-phthalimido, 1-pyrrolidinyl, 4-morpholino, 1-piperazinyl or 4-substituted-1-piperazinyl; Ar is 2, 3 or 4-pyridinyl, 2 or 3-thienyl, phenyl or phenyl substituted by 1 to 3 radicals selected from halo, loweralkyl, loweralkoxy, trifluoromethyl or nitro and may be the same or different; alk1 is a straight or branched hydrocarbon chain containing 1-8 carbon atoms; Z is hydrogen, halogen, loweralkyl, loweralkoxy, hydroxy or nitro; Y is hydrogen or 1-2 radicals selected from loweralkyl, loweralkoxy or hydroxy and may be the same or different, and the acid addition salts thereof.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4994473-A
priorityDate 1984-04-06^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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