http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-114105980-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_757d618b148706bef2dd534eca5f6664
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-16
filingDate 2021-12-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_51a5b7907871c70cbc916224a97240d3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_317cfc728a9d1ad3b3fd54c467655a6a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_259ae427d75099f90e8b23062b73a8a6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_333143d35e3d0a08f744f3455ad47cc9
publicationDate 2022-03-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-114105980-A
titleOfInvention Preparation method of rumepilone intermediate compound and rumepilone intermediate compound
abstract The invention is suitable for the technical field of drug synthesis, and provides a preparation method of a rumepilone intermediate compound and the rumepilone intermediate compound; the invention utilizes Ir-ZhaoPhos asymmetric hydrogenation to construct the chiral compound 2, has high enantioselectivity, high conversion efficiency (S/C is 5000-; further derivatization is carried out on the obtained chiral compound 2a, benzene ring bromination treatment, copper catalysis C-N coupling, debromination and amide reduction are carried out to obtain the rumepilone key intermediate 7, and the synthesis of the rumepilone key intermediate 7 by the compounds 2b, 2C and 2d does not comprise bromination and debromination steps, so that the method is economic and environment-friendly.
priorityDate 2021-12-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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