http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8338142-B2

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D211-60
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filingDate 2008-02-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2012-12-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e8ff0d2df6dea71888d6dd53b9d89419
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b97aa5177234b0ccaad2feb050fb3349
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publicationDate 2012-12-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-8338142-B2
titleOfInvention Method for producing optically active 3-aminopiperidine or salt thereof
abstract The present invention relates to a method for producing an optically active 3-aminopiperidine or salt thereof. In the method, a racemic nipecotamide is stereoselectively hydrolyzed to obtain an optically active nipecotamide and an optically active nipecotic acid in the presence of an enzyme source derived from an organism, and then the optically active nipecotamide is derived into an optically active aminopiperidine or salt thereof by aroylation, Hofmann rearrangement, deprotection of the amino group and further deprotection; or the optically active nipecotamide is derived into an optically active aminopiperidine or salt thereof by selective protection with BOC, Hofmann rearrangement and further deprotection. It is possible by the present invention to produce an optically active 3-aminopiperidine or salt thereof useful as a pharmaceutical intermediate from an inexpensive and easily available starting material by easy method applicable to industrial manufacturing.
priorityDate 2007-02-19-04:00^^<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: 556.