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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-06
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-06
filingDate 1996-03-11^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1999-07-07^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8f0633afcc15df184a08c5d7b3b38406
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c7b2c480e69884f0c1a47cdf9bd6e575
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publicationDate 1999-07-07^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0815101-B1
titleOfInvention PROCESS TO MAKE HIV PROTEASE INHIBITOR FROM 2(S)-4-PICOLYL-2-PIPERAZINE-t-BUTYLCARBOXAMIDE
abstract A process for making a clinically efficacious HIV protease inhibitor eliminates one step in its synthesis, by an alternative convergent synthesis using 2(S)-4-picolyl-2-piperazine-t-butylcarboxamide as an intermediate; as indicated above.
priorityDate 1995-03-15^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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