http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-105801565-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-04 |
| filingDate | 2014-12-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2020-04-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2020-04-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-105801565-B |
| titleOfInvention | Preparation method of N- [ 3-chloro-4- [ (3-fluorophenyl) methoxy ] phenyl ] -6- [ (5-formyl) furan-2-yl ] -4-quinazolinamine |
| abstract | N- [ 3-chloro-4- [ (3-fluorophenyl) methoxy group]Phenyl radical]-6- [ (5-formyl) furan-2-yl]-4-quinazolinamine (IV) synthesis method, Grignard reagent (III) prepared from 5-bromo-2-furaldehyde ethylene glycol (II) and N- [ 4-3-chloro-4- [ (3-fluorophenyl) methoxyl group]Phenyl radical]The (I) -6-iodine-4-quinazolinamine reacts under the catalysis of iron acetylacetonate, and the reaction formula is 。 |
| priorityDate | 2014-12-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 60.