http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2138535-A1

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D473-18
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D473-32
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filingDate 1997-07-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_55f680f4a031fad8412c0d4a9e1106ff
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2eb7ae4060d922fb3c0460ed867230b2
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publicationDate 2000-01-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2138535-A1
titleOfInvention PROCEDURE FOR THE PREPARATION OF THE ANTIVIRAL COMPOUNDS PENCICLOVIR AND FAMCICLOVIR.
abstract Procedure the preparation of the antiviral compounds penciclovir and famciclovir. A process for the preparation of penciclovir or famciclovir comprising one or more of the following steps: a) forming a purine by imidazole or pyrimidine ring closure; b) reacting a purine with a suitable 9-side chain precursor intermediate; c) converting the side chain at position 9 to 4-hydroxy-3-hydroxymethylbut-l-yl or 4-acetoxy-3-acetoxymethylbut-l-yl d) converting a purine to guanine or 2-aminopurine; characterized in that the purine has the formula (I): in which X{sub,1, is SH or S-Z-R{sub,3, (Z is optional) and is straight or branched chain alkylene and R{sub,3 is alkyl , aryl or heteroaryl, X{sub,2 is SH, hydrogen, or a group that can be converted thereto; R{sub,1 , is amino or a group that can be converted to it; and R{sub,2, is hydrogen or a side chain precursor at position 9. Said purine of formula (T) is converted to famciclovir or penciclovir by subsequent transformations.
priorityDate 1996-07-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 39.