http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2014531457-A
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D211-34 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D211-22 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D211-70 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-5407 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-4006 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-04 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D211-34 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-06 |
| filingDate | 2012-09-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2014-11-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2014531457-A |
| titleOfInvention | Improved method for preparing 2-[(2E) -2-fluoro-2- (3-piperidinylidene) ethyl] -1H-isoindole-1,3 (2H) -dione |
| abstract | The present invention relates to an antibacterial compound 7-[(3E) -3- (2-amino-1-fluoroethylidene) -1-piperidinyl] -1-cyclopropyl-6-fluoro-1,4-dihydro-8-methoxy. 2-[(2E) -2-fluoro-2- (3-piperidinylidene) ethyl] -1H-isoindole-1,3 (2H), an intermediate in the synthesis route of -4-oxo-3-quinolinecarboxylic acid -Relates to an improved process for preparing diones, or salts thereof. |
| priorityDate | 2011-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 116.