http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-102147971-B1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2f953e662f0f4a6aedb6f11302833d60
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D249-06
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D249-06
filingDate 2019-11-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2020-08-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_20a24bfb7d129437dc3747a63a2e5838
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ec1689c3583dc76e4fec4f596651b6be
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_992e613c6c01f96940c1c187aca9c055
publicationDate 2020-08-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-102147971-B1
titleOfInvention Method for preparing chemoselective triazole derivatives through miscibility with reaction solvent
abstract The present invention relates to a method for producing a chemoselective triazole using a difference in miscibility with a reaction solvent, and more specifically, two or more alkyne compounds having different miscibility with a reaction solvent; Or two or more azide compounds having different miscibility with the reaction solvent; as the main raw material, and using the difference in miscibility with the reaction solvent, the chemical selective azide-alkyne cyclic addition reaction (Chemoselective cycloaddition reaction) step; And obtaining a 1,4-disubstituted-1,2,3-triazole compound through post-treatment after the cyclic addition reaction. It relates to a method for producing a chemoselective triazole comprising a.
priorityDate 2019-11-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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