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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D295-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D233-32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D207-273
classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-26
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-27
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-273
filingDate 1985-02-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1988-08-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1988-08-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0154490-B1
titleOfInvention Process for the preparation of pyrrolidone derivatives
abstract Process for preparing pyrrolidinone derivatives (1)in which R is hydrogen, alkyl or acyl characterised in that a compound of (2)wherein R' is hydrogen and R<sup>2</sup> is benzyl or substituted benzyl, or R' and R<sup>2</sup> can together form a groupwhere R<sup>4</sup> and R<sup>5</sup> are independently hydrogen, alkyl, phenyl or optionally substituted aryl or together are 1,4-butylene or 1,5-pentylene; R<sup>3</sup> is hydrogen or straight or branched alkyl of 1 to 4 carbon atoms; and X is alkyl subjected to N-deprotection and the deprotected intermediate is cyclized intramolecularly. The deprotected intermediates can be isolated as acid-addition salts.
priorityDate 1984-02-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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