http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2331545-A2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_f3166d2820b5872ab84d235e5fae1d45
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D487-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-04
filingDate 2009-08-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_70854f3cb998ddddf19c241e39ab07fb
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0cf064c4d28a32a67685895d080b3491
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_81fbd2217463bf4763c167101bfb3456
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_654b5678e93ef0c10e41ffcb0820651a
publicationDate 2011-06-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-2331545-A2
titleOfInvention Improved process for preparation of (2r)-4-oxo-4-[3- (trifluoromethyl)-5,6-dihydro [1,2,4]-triazolo[4,3-a]pyrazin- 7(8h)-yl]-l-(2,4,5-trifluorophenyl)butan-2-amine&new impurities in preparation thereof
abstract The present invention relates to synthesis of β-amino acid derivatives of formula (I) and its salts of formula (Ia) by a novel process. The process comprises the reduction of a protected or unprotected prochiral β-amino acrylic acid or derivative there of, by using borane containing reducing agents at atmospheric pressure. The resulting racemic β-amino compound is resolved to a pure stereoisomer of formula (I), specifically to (2R)-4-oxo-4- [3-Ctrifluoromethyl)-5, 6-dihydrol [1,2,4]triazolo [4,3-alpyrazin-7(8H)-yl]-1-(2,4,4-trifluorophenyl)butan-2-amine. In an embodiment the invention disclosed polymorphic forms of formula (I), phosphate salt of formula (I) and also a Dibenzoyl-L-tartaric acid salt of formula (I).
priorityDate 2008-08-27-04:00^^<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: 488.