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filingDate 1993-01-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_eb2cdcc03691bed2db53855bd50af238
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5d80533789506d064ed213c43c30f831
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5373ccf401dad61fc91e65d5aa399e00
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publicationDate 1993-11-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H05306243-A
titleOfInvention Fluorinated cyclobutyl purines and pyrimidines
abstract (57) [Summary] (Modified) [Purpose] 3-Fluoro-3 with antiviral activity -Hydroxymethyl-2- (hydroxy or hydroxymethyl) cyclobutane and its intermediates, as well as methods for making the compounds are provided. A compound represented by the illustrated structural formula, a pharmaceutically acceptable salt thereof, and a cyclobutanal intermediate for synthesizing the compound. [Wherein R 1 is a (substituted) 9H-purin-9-yl group, a (substituted) 2,4-dioxotetrahydropyrimidin-1-yl group, a (substituted) 2-oxo-4-amino-dihydropyrimidin-1 be-yl group; R 6 is OH, CH 2 OH, - O-PO 3 H 2, -CH 2 -O-PO 3 H 2, -O-C O-R 3, be -CH 2 -O-CO-R 3 ; R 7 is H, -PO 3 H 2, be a -CO-R 3; R 3 is H, aryl, C 1 to 10 alkyl or the like R 4 is F, C 1, CF 3 , ethyl and the like. ] The compound shown by these, and its pharmaceutically acceptable salt.
priorityDate 1992-01-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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