http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102863359-B
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_869620724535c26b3e814325a37a5104 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C277-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C279-16 |
| filingDate | 2012-05-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2014-05-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1f602f349c93b8e3dc80f74dacd75a61 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e39ef50902d58702bc12437bd778cafd http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c17f84308fdbd7fc4f1dd0d263114b46 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b2d3d5622627f44f50d0ae6fa353b042 |
| publicationDate | 2014-05-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-102863359-B |
| titleOfInvention | Synthesis method of anti-flu medicine |
| abstract | The invention provides a synthesis method of anti-flu medicine, which takes (+/-) 2-azabicyclo (2, 2, 1) hepta-5-alkene-3 ketone, 2-ethylbutyraldehyde and 1, 2, 4-triazole-1-semiamitraz chloride as main starting materials, and can be used for synthesizing the target product by reactions including ring opening, condensation, esterification, reduction and the like. The synthesis method has the advantages of being fewer in reaction steps, simple and convenient in operation, easy in obtaining of raw materials, controllable in isomer impurities and the like, and has the total recovery rate of 25%, thus being suitable for industrial production. |
| priorityDate | 2012-05-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 74.