http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2516384-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_fd048f86dea957a0403c59240263abcb
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C235-74
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C227-34
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C229-08
filingDate 2010-12-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a3931b391500327acdb4aafe8d93742b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_89d9f761491d155aa3b27dd441150e3e
publicationDate 2012-10-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-2516384-A1
titleOfInvention Novel method for the preparation of (s)-pregabalin
abstract Method for the preparation of a salt (III) of pregabalin and (S)-mandelic acid with a (S, S) diastereomer content greater than 80% which comprises the following steps: (a) Hofmann reaction of (±)-3-(carbamoylmethyl)-5- methylhexanoic acid (I) to obtain racemic pregabalin (II), (b) addition of (S)-(+)-mandelic acid to obtain the corresponding diastereoisomeric salt (III) with a (S, S) diastereomer content greater than 80% (c)optionally, purification of the salt obtained in step (b); characterized in that step(b) is performed without isolating the product obtained in step(a).
priorityDate 2009-12-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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