http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2018070607-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_bb75b0b19820e3833ebdcb31603b242b |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P43-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4245 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D271-06 |
| filingDate | 2017-10-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1216428faef4d608c78af1bbf4a99dc4 |
| publicationDate | 2018-05-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2018070607-A |
| titleOfInvention | Method for producing oxadiazole derivative substituted with amino group |
| abstract | An intermediate of an oxadiazole derivative substituted with an amino group and having an NPY Y5 receptor antagonistic activity, and a production method thereof. The compound represented by formula (I) is selected from substituted / unsubstituted imidazole, substituted triazole, substituted pyrazole, substituted pyrrole, substituted / unsubstituted benzimidazole, substituted benzotriazole, and substituted benzopyrazole. An intermediate that is a salt with one basic compound. Oxadi substituted with an amino group having NPY Y5 receptor antagonistic activity comprising reacting the salt with a halogenating agent and a base, optionally in the presence of a basic compound forming the salt A method for producing an azole derivative. [Selection figure] None |
| priorityDate | 2016-10-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
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