http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2022315532-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_396baecaa471def313eb2a11d1f84b7c
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-04
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-14
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-04
filingDate 2020-06-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e81529318d4150dd478cfe75bc267f44
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e612ee4d33375e181e5c7d9747f77db8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5a7e6f9f6ebe376b91edad41df81052e
publicationDate 2022-10-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2022315532-A1
titleOfInvention Methods for preparing cdk4/6 inhibitor and salt and intermediate thereof
abstract The present invention relates to methods for preparing 5-fluoro-4-(7′-fluoro-2′-methylspiro[cyclopentane-1,3′-indol]-5′-yl)-N-(5-(1-methylpiperidin-4-yl)pyridin-2-yl)pyrimidin-2-amine and a salt and an intermediate thereof The methods provided herein have improved the existing synthesis methods, simplified the preparation process and increased the yield and purity, and can well meet the requirement of large-scale industrial manufacture.
priorityDate 2019-06-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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