http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S61291579-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_cac023d2e2874224ecbbcccbdea1fc91 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P25-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-495 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D295-18 |
| filingDate | 1985-06-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3a448bec9a4a861e4313617c742f68a1 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_20cfdef16c7f477abc7944d9eb37159c http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8b40a7fa5c4331e272ace830bd007b6f http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1084223b1ef675a6d3ce10003daa1df5 |
| publicationDate | 1986-12-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-S61291579-A |
| titleOfInvention | 1-(3-cinnamyl)-4-isopropylcarbamoylpiperazine and production thereof |
| abstract | NEW MATERIAL:1-(3-Fluorocinnamyl)-4-isopropylcarbamoylpiperazine shown by the formula I or its acid addition salt. n USE: A drug and an analgesic having improved analgesic activity and weak narcotic properties. n PREPARATION: 3-Fluorocinnamyl chloride and piperazine are directly melted to give 1-(3-fluorocinnamyl)piperazine shown by the formula II is reacted with isocyanic acid isopropyl ester in a solvent such as benzene, etc., in the presence of a basic catalyst such as tertiary amine, etc., or in the absence of it, at 0W50°C to give a compound shown by the formula I. n COPYRIGHT: (C)1986,JPO&Japio |
| priorityDate | 1985-06-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 34.