http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1237846-A1

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C2601-02
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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C229-28
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C229-28
filingDate 2000-12-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f9a8bfd602b19dd72571ac936c33f516
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f2f8035b5fe8731bdc80854a5a86cf16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_de336fa51586dd4882c7fa4489ec482b
publicationDate 2002-09-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1237846-A1
titleOfInvention Preparation of 3-amino-3-cyclopropylpropanoate esters
abstract Disclosed is a process for preparing substantially enantiomerically pure 3-amino-3-cyclopropylpropanoate esters, i.e., esters of 3-amino-3-cyclopropylpropanoic acid (3-cyclopropylalanine esters or 3-CPA esters) by a 5-step process wherein cyclopropanecarboxaldehyde (CPCA) is reacted with malonic acid and a source of ammonia to obtain 3-cyclopropylalanine (3-CPA); esterifying the 3-CPA; contacting the 3-CPA ester with a substantially enantiomerically pure acid selected from tartaric acid, dibenzoyltartaric acid and mandelic acid to obtain a diastereomeric salt of the 3-CPA ester and the acid; recrystallization of the salt to substantial diastereomeric purity; and neutralizing the salt to afford the substantially enantiomerically pure 3-CPA ester.
priorityDate 1999-12-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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