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filingDate 1989-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1995-08-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2a5feffc430b410a8008dcd3f368f31c
publicationDate 1995-08-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5440040-A
titleOfInvention Pyrimidine intermediates
abstract PCT No. PCT/SE89/00322 Sec. 371 Date Jan. 18, 1991 Sec. 102(e) Date Jan. 18, 1981 PCT Filed Jun. 7, 1989 PCT Pub. No. WO89/12061 PCT Pub. Date Dec. 14, 1989.The present invention is directed to compounds of formula (I), <IMAGE> (II) wherein R1 is OH, NH2; R2 is a heteroaromatic or aromatic substituent; R3 is H, OH, F, OCH3; R4 is H, F, OH or an ether or ester residue thereof, OCH3, CN, C=CH, N3; R5 is OH or an ether or ester residue thereof including mono, di- and triphosphate esters ( alpha ), wherein n is 0 or 1 and M is hydrogen or a pharmaceutically acceptable counterion such as sodium, potassium, ammonium or alkylammonium; and pharmaceutically acceptable salts thereof; and pharmaceutical compositions comprising said compounds can be used for therapeutic treatment of virus infections. The present invention is also directed to compounds of formula (I'), <IMAGE> (I') wherein R1 and R2 are as defined above, as intermediates.
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