http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CS-217880-B1
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_bf6e011c6a5445954e7766d5c2945559 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 |
Incoming Links
Total number of triples: 46.