http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-100567292-C
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_f2d3599fb8f8f479dba95ca9bb504884 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P43-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-06 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-06 |
| filingDate | 2005-04-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2009-12-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7dda9eca61c69eca842487f4ce934fb5 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8cc1400ffefddf18ec0eee1b01178bec http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b132115f5801174f9164cc4eda9a8fed |
| publicationDate | 2009-12-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-100567292-C |
| titleOfInvention | The cis-selectivity synthetic method of preparation imidazolium compounds |
| abstract | Preparation enantiomorph 6-[amino (4-chloro-phenyl-) (1-methyl isophthalic acid H-imidazoles-5-yl) methyl]-the cis-selectivity synthetic method of 4-(3-chloro-phenyl-)-1-methyl-2 (1H)-quinolinone, described method comprises (±)-6-[chlorine (4-chloro-phenyl-) (1-methyl isophthalic acid H-imidazoles-5-yl) methyl]-4-(3-chloro-phenyl-)-1-methyl 2 (1H)-quinolinone is converted into (VIII) compound, and wherein aryl is by Cn 1-6 Alkoxyl group one or dibasic phenyl or by Cn 1-6 Alkoxyl group one or dibasic naphthyl. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-10954210-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-11639341-B2 |
| priorityDate | 2004-05-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 118.