http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2010069625-A1

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H19-06
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filingDate 2008-03-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_47a7bb8f466dfc9de76eeca76ce6687b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ea2f4f09e2b722eef0878bca4b134941
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_20f9bcbbd8f6db50e141deb7f428df71
publicationDate 2010-03-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2010069625-A1
titleOfInvention Process for preparing of 2'-deoxy-2'2'-difluorocytidine
abstract Disclosed is a method for preparing 2′-deoxy-2′,2′-difluorocytidine of Formula I comprising, preparing an optically pure 3R-hydroxypropane amide compound of Formula VIII from an optical ester compound of Formula IX using an optically active chiral amine, preparing an optically pure D-erythro-2,2-difluoro-2-deoxy-1-oxoribose compound of Formula V from the compound of Formula VIII, glycosylating the compound of Formula V with a nucleobase to prepare the 2′-deoxy-2′,2′-difluorocytidine of Formula I as a β-nucleoside. With the present invention, it is possible to prepare an optically pure compound of Formula I in a high purity and a high yield. In the Formulae, R 1 and R 2 are protecting groups and are each independently benzoyl, 4-methylbenzoyl, 3-methylbenzoyl, 4-cyanobenzoyl, 3-cyanobenzoyl, 4-propylbenzoyl, 2-ethoxybenzoyl, 4-t-butylbenzoyl, 1-naphthoyl or 2-naphthoyl, R 3 , R 4 and R 7 are each independently C 1 -C 3 alkyl, R 5 is methyl or ethyl, R 6 is hydrogen, methyl or methoxy.
priorityDate 2007-03-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 448.