http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-101747267-B
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1ce61bf06f294f2f466c067ed41cc8ce |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D215-227 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D215-18 |
| filingDate | 2010-01-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2011-07-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_81931229363b71b9499e377dabaa36da http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2b103045a5521dcc78e18fa5823bd677 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8121f9d024fd05fa391199a5989c6042 |
| publicationDate | 2011-07-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-101747267-B |
| titleOfInvention | Method for synthesizing 4-substituted-3-chlorine-2-carbostyril |
| abstract | The invention discloses a method for synthesizing 4-substituted-3-chlorine-2-carbostyril which is a compound shown as the general formula I. In the method, 2-Chloro-2-ethyl acid phosphate and a compound shown as the formula II are used as starting raw materials; a compound shown as the formula III can be prepared firstly by acylation reaction; and finally the compound shown as the formula I is obtained by intramolecular Horner-Wadsworth-Emmons reaction. The invention has the advantages of strong generality, simple operation, moderate reaction condition, high product yield, cheap and easily obtained raw materials and bright application prospects. |
| priorityDate | 2010-01-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
| Predicate | Subject |
|---|---|
| isDiscussedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID466313869 http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID467872843 |
Total number of triples: 16.