http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H04352763-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_44c713790ce00813da2e6c6d57a29456 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P25-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P43-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C317-44 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P9-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P25-00 |
| filingDate | 1991-04-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6420bfa36ec0801b6ea3d4cb3004bea9 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_09d411ceee278221de02913dae10f912 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e682332b031023f6a77d3f03e2875f57 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2e2d1c4136631fafca72b2b3e4a3e604 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4b83a658c9848925a1355d0d6d0ba07b |
| publicationDate | 1992-12-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-H04352763-A |
| titleOfInvention | Sulfonylalkanoic acid amide derivative |
| abstract | PURPOSE: To obtain a new compound useful as a treating agent for painful muscle spasm following locomotorium diseases such as dorsolumbar pain or herniated disk, having muscle relaxing action, rigidity remitting action and a treating agent for spastic paralysis such as cerebrovascular disorder. n CONSTITUTION: A compound shown by formula I (X is halogen; Y is H or halogen) such as N-cyclopropyl-2-(2-boromophenylsulfonyl)propionamide. The compound shown by formula I is obtained by reacting a phenylthioalkanoic acid shown by formula II or an active derivative thereof with cyclopropylamine to give a sulfide compound shown by formula III. Then this compound shown by formula III is reacted with an oxidizing agent (e.g. m-chlorobenzoic acid) shown by formula III in a solvent such as dichloromethane at 0-150°C to give a drug having durability and low side effects. n COPYRIGHT: (C)1992,JPO&Japio |
| priorityDate | 1990-04-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 32.