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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5deddb47ccaab1d4da2aacc344dd8717
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D267-22
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D267-22
filingDate 1981-09-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1986-12-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_880ad195686b9fede375c1c9acb2baf3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9dce72be039647df26c725d670b20ee8
publicationDate 1986-12-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4626522-A
titleOfInvention Benzoxazocines intermediates
abstract Novel benzoxazocines of formula (I) ##STR1## and their pharmaceutically acceptable acid addition salts, wherein R 1 represents hydrogen, or one or more halogen, trifluoromethyl, lower alkyl, lower alkoxy, nitro, amino acylamino, mono- or di- (lower)alkyl-amino or cyano substituents, R 2 , R 3 and R 4 , which may be the same or different, each represent hydrogen or lower alkyl or R 3 and R 4 together represent --(CH 2 ) 3 --or --(CH 2 ) 4 --, R 5 represents hydrogen, lower alkyl, phenyl(lower)alkyl or cycloalkyl(lower)alkyl, and Ar is a phenyl radical optionally substituted by one or more halogen, trifluoromethyl, lower alkyl, lower alkoxy, nitro or amino groups exhibit activity on the central nervous system, particularly as antidepressants. The compounds can be prepared from novel alcohols of formula (II) ##STR2## wherein R 1 , R 2 , R 3 , R 4 , R 5 and Ar are as defined above and X is fluorine, chlorine or bromine.
priorityDate 1980-01-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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