http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-111978320-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2a546f102ed9457841341733de240a25
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04
filingDate 2020-09-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f08f84400c36230f4c211ab92f3d7b12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a9a196da48399bd0e33028376de61efd
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_31e63f20da8a8f9ebd6dcb1cdd12ae73
publicationDate 2020-11-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-111978320-A
titleOfInvention A kind of synthetic method of 1H-pyrrole[3,2-c]pyridine-6-ol
abstract The invention provides a method for synthesizing 1H-pyrrole[3,2-c]pyridine-6-alcohol, which relates to the technical field of chemical intermediate synthesis. Reaction with benzyl alcohol to generate 6-(benzyloxy)-1H-pyrrolo[3,2-c]pyridine, 6-(benzyloxy)-1H-pyrrolo[3,2-c]pyridine after hydrogenation and debenzylation Obtain 1H-pyrrole[3,2-c]pyridine-6-alcohol; effectively solve the problem of converting chlorine to hydroxyl on 6-chloro-5-azaindole, and successfully prepare 1H-pyrrole[3,2-c]pyridine -6-alcohol product; the method of the present invention has a short method route, raw materials and reagents are commercially available, no dangerous and toxic chemical reagents are used, the reaction conditions are mild, the operation is simple, and the scale-up production is easy.
priorityDate 2020-09-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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