http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100345568-B1
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D239-90 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-91 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-88 |
| filingDate | 2000-04-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2002-07-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2002-07-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | KR-100345568-B1 |
| titleOfInvention | A new method for the synthesis of 2-(fluoromethyl)-3-aryl-4(3h)-quinazolinone derivatives |
| abstract | The present invention relates to a new method for synthesizing 2- (fluoromethyl) -3-aryl-4 (3H) -quinazolinone derivatives, and in particular, the present invention is less reactive than fluoroacetyl chloride. By using safe and easy-to-use sodium fluoroacetate as a reactant and adjusting the reaction conditions, the quinazolinone is equivalent to or better than the conventional method in terms of yield and quality of the produced product, while increasing the safety of the process. A method for synthesizing derivatives is provided. In addition, the new synthesis method of the quinazoline derivative according to the present invention is improved in the overall process, the process efficiency is improved in the reaction conditions, yield, etc. and is easy to manufacture. |
| priorityDate | 2000-04-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 50.