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filingDate 2004-04-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2009-06-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c2aa75685fce8e828d4ea87c155e4e2d
publicationDate 2009-06-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2358979-C2
titleOfInvention Modified fluorinated nucleoside analogues
abstract FIELD: chemistry. n SUBSTANCE: present invention relates to (2'R)-2'-dezoxy-2'-fluoro-2'-C-methylnucleoside (β-D or (β-L) n , where X represents O; R 1 and R 7 independently represent H; R 3 represents hydrogen and R 4 represents NH 2 ; or its pharmaceutically acceptable salt. The invention also pertains to the method of producing the said compounds, which involves glycosylation of N 4 -benzoylcytosine with a compound of formula 1-4, where R represents methyl, Pg is chosen from C(O)Ph, CH 2 Ph or both Pg groups can be included in 1,3-(1,1,3,3-tetraisopropyldisiloxanylidene); with further removal of protection of 3'-OPg and 5'-OPg and N-benzoyl of the obtained product. n EFFECT: invented compounds or their pharmaceutically acceptable salts are used as active ingredients against Flaviviridae family viruses in pharmaceutical compositions and liposomal pharmaceutical compositions. n 4 cl, 9 tbl, 5 ex, 4 dwg
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-11575766-B2
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priorityDate 2003-05-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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