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filingDate 2000-12-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e38ebd5cee174b0316045625496035ee
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publicationDate 2001-06-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2001004668-A1
titleOfInvention Process for the preparation of purine derivatives
abstract The present invention provides a process for the synthesis of penciclovir and famciclovir by 9-substituting 2-amino-6-chloropurine (ACP) with an appropriate side chain precursor, followed by conversion of the 6-chloro moiety to a hydroxy moiety (i.e. to form a guanine) or hydrogen (to form a 2-aminopurine), respectively.
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priorityDate 1983-08-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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