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filingDate 2011-03-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2017-03-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_712f1bf752ae705c3a6222ba3c4455e4
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publicationDate 2017-03-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-9586893-B2
titleOfInvention Processes and intermediates for preparing a macrocyclic protease inhibitor of HCV
abstract A process for preparing [(1R,2R)-4-oxo-1,2-cyclopentanedicarboxylic acid II, by the resolution of racemic 4-oxo-1,2-cyclopentanedicarboxylic acid (V), said process comprising:n (a) reacting 4-oxo-1,2-cyclopentanedicarboxylic acid (V) with brucine or (1R,2S)-(−)-ephedrine, thus preparing the bis-brucine or bis-(1R,2S)-(−)-ephedrine salt of (V), and (b) precipitating selectively the bis-brucine or bis-(1R,2S)-(−)-ephedrine salt of (1R,2R)-4-oxo-1,2-cyclopentanedicarboxylic acid II, while the bis-brucine or bis-(1R,2S)-(−)-ephedrine salt of [(1S,2S)-4-oxo-1,2-cyclopentanedicarboxylic acid stays in solution; (c) liberating the acid II by removal of brucine or (1R,2S)-(−)-ephedrine from the precipitated salt obtained in step (b).
priorityDate 2010-03-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 521.