http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2008065490-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 2007-11-13^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cbb77aa72a42562304f2b46931f95a39
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publicationDate 2008-06-05^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2008065490-A2
titleOfInvention Process for the preparation of atazanavir
abstract The invention relates to a process for the preparation of Atazanavir, which comprises reacting the hydrochloride salt of compound (6) with N-methoxycarbonyl-L-tert-leucine, the removal of the benzyloxycarbonyl group and the reaction with methoxycarbonyl chloride. The process is particularly advantageous in that it allows to use reduced amounts of N-methoxycarbonyl-L-tert-leucine and avoids the use of unstable intermediates.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2011107843-A3
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2011107843-A2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2013014633-A1
priorityDate 2006-11-28^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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