http://rdf.ncbi.nlm.nih.gov/pubchem/patent/PE-20110098-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6572ff5df928fd17340eb2a8cb6d8502 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P9-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P9-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P9-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D223-16 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P9-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-55 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-16 |
| filingDate | 2010-03-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_17c712689c4cbb8346249b2bd987b93c http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8892aacc8c6323a4fe2c603e3d1fe957 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e9b15ed87f587a97ef3c71d0b76ceae0 |
| publicationDate | 2011-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | PE-20110098-A1 |
| titleOfInvention | NEW PROCEDURE FOR THE SYNTHESIS OF IVABRADINE AND ITS SALTS BY ADDITION TO A PHARMACEUTICALLY ACCEPTABLE ACID |
| abstract | IT REFERS TO A SYNTHESIS PROCESS OF THE COMPOUND 3- {3 - [{[(7S) -3,4-DIMETOXIBICICLO [4.2.0] OCTA-1,3,5-TRIEN-7-IL] METIL} (METTIL) AMINO] PROPYL} -7,8-DIMETOXI-1,3,4,5-TETRAHIDRO-2H-3-BENZAZEPIN-2-ONA (IVABRADINA) AND OF ITS SALTS OF ADDITION TO AN ACID SELECTED FROM THE ACIDS HYDROCHLORIC, BROMHIDRICO, SULFURIC, AMONG OTHERS; THAT INCLUDES A) THE REACTION BETWEEN THE COMPOUND 3,4-DIMETOXIBICICLO [4.2.0] OCTA-1,3,5-TRIENO-7-CARBONITRILE AND 7,8-DIMETOXI-3- [3- (METTILAMINO) PROPIL] - 1,3,4,5-TETRAHYDRO-2H-3-BENZAZEPIN-2-ONA IN THE PRESENCE OF A TRANSITIONAL SALT SELECTED FROM COPPER CHLORIDE, YTRIUM (III) TRIFLUOROMETHANOSULPHONATE, LANTHANE (III) TRIFLUOROMETHANOSULPHONATE, AMONG OTHERS; IN A SOLVENT SELECTED FROM ETHANOL, DIMETHYLSULFOXIDE, N-METHYLPYRROLIDINE, AMONG OTHERS. B) THE ADDITION OF A SELECTED PROTON DONOR AGENT OF SODIUM TETRABOROHYDRIDE, SODIUM CYANOBOROHYDRIDE, BORANOMORPHOLINE COMPLEX, AMONG OTHERS. SUCH PROCESS IS USED TO PRODUCE IVABRADINE WITH A YIELD OF AT LEAST 33%. BEING USEFUL IN THE TREATMENT OR PREVENTION OF ANGINA PECTORIS, MYOCARDIAL INFARCTION, ASSOCIATED RHYTHM DISORDERS, AMONG OTHERS |
| priorityDate | 2009-03-31-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 39.