http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-8604113-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_dec2e56e07ad5aa00ac66bef80947360 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-195 |
| filingDate | 1985-05-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 1986-01-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | ES-8604113-A1 |
| titleOfInvention | ALTERNATIVE PROCEDURE FOR THE SYNTHESIS OF ACID O- (2,6-DICHLOROANILINO) FENIL ACETICO |
| abstract | PROCEDURE FOR OBTAINING THE ACID 0- (2,6-DICHLOROANILINO) PHENYL ACETIC. IT INCLUDES THE REACTION OF 2,6-DICHLOROANILINE WITH 0-METOXIMETYLODOBENZENE, IN THE PRESENCE OF A CATALYST, WITH AGITATION, AT A TEMPERATURE OF 100JC; FOLLOWED BY CRYSTALLIZATION OF THE 0- (2,6-DICHLOROANILINE) METOXIMETHYL BENENE AND REACTION OF THIS WITH HYDRO YORIC ACID AT A TEMPERATURE NOT HIGHER THAN 100JC; REACTION WITH POTASSIUM CYANIDE IN A HYDROALCOHOLIC MEDIUM TO FORM THE 0- (2,6-DICHLOROANILINE) PHENYL ACETONITRILE, WHICH IS SAPONIFIED WITH SULFURIC ACID AND WATER, TO OBTAIN THE 0- (2,6-DICHLOROANILINE) PHYLOROANILINE ACID IT IS PURIFIED BY RECRISTALIZATION IN PETROLEUM ETER-ETER. THIS COMPOUND HAS APPLICATIONS IN PHARMACOLOGY FOR ITS ANTI-INFLAMMATORY ACTIVITY. |
| priorityDate | 1985-05-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 26.