http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-108690018-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D513-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-04 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D513-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04 |
| filingDate | 2018-06-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2021-01-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2021-01-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-108690018-B |
| titleOfInvention | Preparation method of imidazo [1,2-a ] pyridine derivative |
| abstract | The invention discloses a preparation method of an imidazo [1,2-a ] pyridine derivative, belonging to the field of organic synthesis. The method takes 2-phenoxyacetophenone compounds as initial raw materials and elemental iodine as a catalyst to react with 2-aminopyridine compounds, and then the imidazo [1,2-a ] pyridine derivatives are obtained by column chromatography separation. Compared with the prior art, the method has the advantages of high reaction yield, simple post-treatment and suitability for industrial production. The prepared imidazo [1,2-a ] pyridine derivative can be used as a prodrug for synthesizing medicaments such as antifungal, anti-inflammatory, antitumor, antiviral, antibacterial, antiprotozoal, antipyretic, analgesic, anti-apoptosis and the like, and can also be applied to the fields of organic photoelectric materials, medicines, biological probes, fluorescent dyes and the like. |
| priorityDate | 2018-06-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 46.