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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D215-40
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D215-40
filingDate 1989-05-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1990-08-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_30fae5dc88be4f3089d5571357a75c0b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_019039578c94a0e8710e2b7bcaac186f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ee70db1d5557ced78299439cc0b4695a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2a682151f92329e0dc23035be69ed0dc
publicationDate 1990-08-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4950760-A
titleOfInvention Decahydroquinolines and 5,6,7,8 tetrahydroquinolines
abstract A compound selected from the group consisting of all enantiomeric and diastereoisomeric forms of a decahydroquinoline of the formula <IMAGE> I wherein R1 is alkyl of 1 to 5 carbon atoms, R2 is selected from the group consisting of hydrogen and alkyl of 1 to 5 carbon atoms, A is selected from the group consisting of -(CH2)n-, -CH2O- and alkylene substituted with alkyl having a total of 2 to 8 carbon atoms, n is an integer from 0 to 5, Z is selected from the group consisting of optionally substituted phenyl, optionally substituted naphthyl, optionally substituted indenyl, optionally substituted heteromonocycle of 5 to 6 members and optionally substituted heterobicycle with the proviso that when Z is o-alkoxy-phenyl, A is not -(CH2)n- in which n is O, and their non-toxic, pharmaceutically acceptable acid addition salts and their quaternary ammonium salts and intermediates having analgesic, diuretic, hypotensive, anti-arrithmic and anti-cerebral-ischaemic properties.
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5317028-A
priorityDate 1986-08-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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