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inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_867f85c9e0616f0c1dcc99d3c2e86f42
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publicationDate 2007-02-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2007013645-A1
titleOfInvention Valacyclovir precursor, valacyclovir and salts thereof, and process for the production of them
abstract A process for the production of 2-[(2-amino-1,6-dihydro-6- oxo-9H-purin-9-yl)methoxy]ethyl N-[(benzyloxy)carbonyl]-L- valinate (3) (Z-valacyclovir) which comprises the step of condensing aciclovir (1) with N-[(benzyloxy)carbonyl]-L-valine (2) in the presence of a condensing agent in a solvent, characterized in that the aciclovir (1) takes the form of a powder having a mean particle diameter of 120µm or below. According to the process, Z-valacyclovir which is reduced in optical isomer content and enhanced in chemical purity can be produced, which makes it possible to provide chemically and optically high-purity 2-[(2-amino-1,6-dihydro-6-oxo-9H- purin-9-yl)methoxy]ethyl L-valinate (valacyclovir) or salts thereof.
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