http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-1329212-C
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_116c851e729089df9a427027272fa290 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D333-20 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J23-44 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D495-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J25-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D333-20 |
| filingDate | 1988-12-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 1994-05-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8dcbbd8c2a387700374fb204726c6e58 |
| publicationDate | 1994-05-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CA-1329212-C |
| titleOfInvention | Process for the preparation of n-(2-chlorobenzyl)-2- (2-thienyl) ethylamine |
| abstract | ABSTRACT This invention relates to a process for the preparation of N-(2-chlorobenzyl)-2-(2-thienyl)-ethylamine, a useful intermediate in the synthesis of ticlopidine which is a platelet aggregation inhibitor. According to the invention N-(2-chlorobenzyl)-2-(2-thienyl)-ethylamine is prepared by reaction of 2-thiophene acetonitrile with 2-chlorobenzylamine and hydrogen in the presence of a hydrogenation catalyst. This process is particularly advantageous since it ensures good yields while being unexpensive. |
| priorityDate | 1987-12-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 40.