http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DD-202705-A5
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_8e0ff16e899ce32685c9600075c1cc21 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-16 |
| filingDate | 1982-03-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5dc5a7f102dd8cb1035bc1c85c260c8a http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b107fa5960345c8be5f0f7fa159960ca |
| publicationDate | 1983-09-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | DD-202705-A5 |
| titleOfInvention | METHOD FOR PRODUCING NEW THIAZONE DERIVATIVES |
| abstract | The invention relates to a process for the preparation of novel thiazole derivatives for use as medicaments. The aim of the invention is the provision of novel thiazole derivatives with valuable pharmacological properties, in particular with antinociceptive and anti-inflammatory action and with an inhibitory effect on prostaglandin synthesis. According to the invention, 2,4,5-trisubstituted thiazoles of the formula I are prepared in which, for example: R 1 and R 2 are independently unsubstituted or aliphatically hydrocarbon radicals, free, etherified or esterified hydroxy, etherified optionally S-oxidized mercapto, aliphatically substituted Amino and / or trifluoromethyl substituted aryl or optionally N-oxidized heteroaryl, X is Thio, is 0, 1 or 2 and R deep 3 is an unsubstituted or etherified by etherified or esterified hydroxy, etherified optionally S-oxidized mercapto and / or in higher than the alpha-position of the oxo and / or hydroxy-substituted, optionally additionally to terminally bonded hydroxy present in salt form sulfo hydrocarbon radical, inter alia |
| priorityDate | 1982-03-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 397.