http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2011107843-A2

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-42
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-42
filingDate 2011-02-16^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8672adb1eda40c19f53bc1d5390d9877
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6d19d16ac9647dbc9329ef732132bc90
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publicationDate 2011-09-09^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2011107843-A2
titleOfInvention Process for the preparation of atazanavir sulfate substantially free of diastereomers
abstract The present invention provides atazanavir sulfate substantially free of diastereomeric impurities. The present invention also provides atazanavir sulfate having D-tertiary leucine analogues less than 0.1%. The present invention further relates to an improved process for preparing atazanavir sulfate, substantially free of its diastereoisomeric impurities, which comprises of reacting diamino compound (IV) with N-methoxycarbonyl-(L)-tertiary-leucine (V) having D-isomer less than 0.1 % to obtain atazanavir base; conversion of atazanavir base to atazanavir sulfate by reacting with sulfuric acid and crystallization of atazanavir sulfate from suitable organic solvent(s).
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