http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-110294757-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-04 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-12 |
| filingDate | 2019-06-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2020-07-31-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2020-07-31-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-110294757-B |
| titleOfInvention | Synthetic method and application for preparing C-3-thioimidazopyridine derivative by copper catalysis one-pot method |
| abstract | The invention relates to a synthetic method for preparing C-3-thioimidazopyridine derivatives by a copper-catalyzed one-pot method. The method takes different substituted o-halogenated aniline, carbon disulfide and substituted imidazopyridine compounds as raw materials, and constructs the C-3-position thioimidazopyridine compound by taking the o-halogenated aniline, the carbon disulfide and the substituted imidazopyridine compounds as the raw materials under the catalysis of copper salt and by Ullmann coupling and C-H bond activation strategies. The method has the advantages of few reaction steps, low cost and the like. The C-3-thioimidazopyridine derivative prepared by the method is expected to be applied as a lead compound in the research and development fields of anti-cancer and anti-virus drugs. |
| priorityDate | 2019-06-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 92.