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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D207-14
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-54
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-14
filingDate 2000-06-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2001-04-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3f9481dfe28fb1495e063f858206d066
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7f127b20da80f3afc38ccf7ee7fa5aaa
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a011385edb968a543218f5a4d3350d56
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_38995cb88cc9d802e675de407e77e156
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_03865b5de178371079a435ba5f798576
publicationDate 2001-04-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-6211395-B1
titleOfInvention Enantioselective synthesis of 3-aminopyrrolidines
abstract The invention relates to a process of preparing a chiral compound of the formula:wherein R1 is selected from the group consisting of hydrogen and lower alkyl, and R2 and R2' are the same, and R2 and R2' are selected from a group consisting of hydrogen and primary alkyl, or R2 and R2' taken together form a C3 to C6 cycloalkyl, comprising the steps of chirally reducing a beta-keto ester to afford a beta-hydroxy ester, activating the beta-hydroxy ester by treatment with a sulfonic acid or a derivative thereof to provide an activated compound having sulfonate leaving group, displacing the sulfonate leaving group with an azido moiety, or treating the activated compound with an alkylamine, deprotecting and cyclizing to afford a pyrrolidinone, and reducing the pyrrolidinone to afford a stereoisomerically preferred 3-aminopyrrolidine derivative.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8729063-B2
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priorityDate 1998-10-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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