http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8242303-B2

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07B2200-07
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C271-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C229-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C233-83
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07B53-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C229-00
filingDate 2008-05-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2012-08-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9eb309be3f206b20842570ef53cd29e8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_585040c1025388c07fa482ac700744e1
publicationDate 2012-08-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-8242303-B2
titleOfInvention Method of producing optically active N-(halopropyl) amino acid derivative
abstract The present invention provides a method for producing an optically active N-(halopropyl)amino acid derivative, wherein the method comprises the steps of obtaining a compound represented by formula (III) by reacting an optically active alanine ester represented by formula (I) or a salt thereof (hereinafter sometimes simply referred to as an “alanine ester”) with a halogenated propane represented by formula (II); and obtaining an optically active N-(halopropyl)amino acid derivative represented by formula (IV) by introducing a protecting group onto the nitrogen atom of the compound represented by formula (III). The present invention provides a method for efficiently producing an optically active N-(halopropyl)amino acid derivative.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2013333640-A1
priorityDate 2007-08-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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