| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_82e1442f9428e3fa955315add7fa5048
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e1769472525e6aaa5510a8560bc4d400
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_dfb5def72daa72bede1f96b990df780f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2375aa0fbd0ba57436e276f5ebc8936c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c9870a89c7ac609c4021c562dea29c9f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_10e4b1416c6e66e0ade5429212414964
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_b5e07888f923b7443f3b8eb913614893 |
| classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D521-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P1-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D403-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D209-88 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-88
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P1-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4178 |
| filingDate |
2003-04-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3312eb75e73ab4101caa6ad275d72c10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_905e6fa19b2f1243abf5d4f5a43831f7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f7801b91dfc5cb19725dcc6fa351e2b9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ffc637f4dae8cb981d651ea5ee7f26bc
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_571b041d8fa9872f90388661789c732a |
| publicationDate |
2003-11-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
WO-03093281-A1 |
| titleOfInvention |
Process for preparing 1,2,3,9-tetrahydro-9-methyl-3-[(2-methyl-1h-imidazol-1-yl)methyl]-4h-carbazol-4-one |
| abstract |
A process for preparing ondansetron by transamination of an ondansetron structural analog that can be readily prepared conveniently by a Mannich reaction is provided. The process represents an improvement upon known procedures for making ondansetron by transamination because of its rapid rate, selectivity and the ease with which the product can be isolated from the reaction mixture. |
| isCitedBy |
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1828141-A4
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1828141-A1 |
| priorityDate |
2002-04-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |