http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-102323972-B1

Outgoing Links

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-61
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D409-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D405-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D409-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-61
filingDate 2020-01-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2021-11-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2021-11-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-102323972-B1
titleOfInvention Preparation method of 4-aryl-2-halopyridine derivatives
abstract The present invention relates to a method for preparing a 4-aryl-2-halopyridine derivative, wherein the method according to the present invention comprises forming γ-enamine of single-activated α,β-unsaturated nitrile, followed by halogen Compared to the conventional method using a double-activated substrate through intramolecular cyclization using a source, there is an effect of high yield and efficient formation of a 4-aryl-2-halopyridine compound under mild conditions.
priorityDate 2020-01-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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