http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2016505068-A
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D239-86 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D211-46 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D239-94 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-517 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-12 |
| filingDate | 2014-01-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2016-02-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2016505068-A |
| titleOfInvention | Process for producing 1- (4- (4- (3,4-dichloro-2-fluorophenylamino) -7-methoxyquinazolin-6-yloxy) piperidin-1-yl) prop-2-en-1-one |
| abstract | The present invention provides a simpler 1- (4- (4- (3,4-dichloro-2-fluorophenylamino) -7-methoxyquinazolin-6-yloxy) piperidine-, compared to prior art methods. The present invention relates to a novel process for producing 1-yl) prop-2-en-1-one. The process of the present invention comprises 4- (3,4-dichloro-2-fluorophenylamino) -7-methoxyquinazolin-6-ol in the presence of a base in an inert protic polar solvent and N-acyl. It is produced by reacting with a piperidine derivative. [Selection figure] None |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2019065034-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-7051929-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2020125306-A |
| priorityDate | 2013-01-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 25.