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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C227-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C229-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D473-18
filingDate 2007-04-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2010-07-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-WO2008139539-A1
titleOfInvention Method for producing valaciclovir
abstract Provided is a production method capable of efficiently obtaining chemically and optically highly pure valaciclovir. Acyclovir represented by formula (2), and formula (1) (wherein R 1 represents an alkyl group, an aryl group or an alkoxyl group, R 2 represents a hydrogen atom or an alkyl group, and R 3 represents an alkyl group. The organic amine salt of N-protected valine represented by the formula (3) or the alkali metal salt or alkaline earth metal salt of N-protected valine is neutralized and subjected to a condensation reaction in the presence of a condensing agent. A method for producing valaciclovir represented by formula (4) or a salt thereof, comprising obtaining N-protected valaciclovir represented by (Each symbol in the formula has the same meaning as in the specification.)
priorityDate 2007-04-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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