http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-WO2004094385-A1
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07B2200-07 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D215-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D215-14 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D215-14 |
| filingDate | 2004-04-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2006-07-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-WO2004094385-A1 |
| titleOfInvention | Process for producing ethyl (3R, 5S, 6E) -7- [2-cyclopropyl-4- (4-fluorophenyl) quinolin-3-yl] -3,5-dihydroxy-6-heptenoate |
| abstract | Using a filler having a polysaccharide derivative supported on a carrier for liquid chromatography, 6E-7- [2-cyclopropyl-4- (4-fluorophenyl) quinolin-3-yl] -3,5-dihydroxy-6 The (3R, 5S, 6E) form is prepared from a solution containing a mixture of the optical isomers of ethyl heptenoate. Part or all of the hydroxyl groups and amino groups of the polysaccharide in the polysaccharide derivative are one or more substituents such as a carbamoyl group in which one hydrogen atom is substituted with an aromatic group having a specific alkyl group. Has been replaced by According to the present invention, the (3R, 5S, 6E) body can be produced with higher productivity than conventional methods. |
| priorityDate | 2003-04-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 56.