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http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_a8095fcbc14f32f140efa46074f127f1
classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D337-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D211-06
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D411-02
filingDate 1981-03-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e8b4d9699502ceefee999e91a5ff10ac
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_651089a790fe6d4fdc73dafbc9a33b81
publicationDate 1983-01-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CS-217880-B1
titleOfInvention Process for preparing a novel amino alcohol derived from 2-chloro-11Hdibenz (b, f) -1,4-oxathiepine
abstract The invention relates to a method of preparationnof new 2-chloro-11- (1-methyl-4-hydroxy-4-n-piperidyl) -1H-dibenz (b, f) -1,4-oxathiepinenand its salts. Named substance and hernsalts are both intermediates for the preparationnneurotrophic drugs, on their ownnexhibit mild trash-inactivity.nThe process of the invention is based on the inventionnin the reaction of 2-phloro-1H-dibenz (b, f) -1,4-oxathiepinenwith butyllithium in ether andnfollowed by 1-methyl-4-piperidone
priorityDate 1981-03-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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