Dihydroxypyridmidine carboxylic acids as viral polymerase...

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...

Reexamination Certificate

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C544S263000, C544S319000, C544S237000, C544S123000, C514S274000, C540S523000

Reexamination Certificate

active

07091209

ABSTRACT:
A class of 2-aryl-4,5-dihydroxy-6-carboxypyrimidines of formula (I): wherein Ar is an optionally substituted aryl or heterocyclicgroup; as well as compounds of formula (I) which are derivatized at one or more of the 4-hydroxy, 5-hydroxy or 6-carboxy groups; and tautomers thereof, and pharmaceutically acceptable salts or esters thereof; and inhibitors of viral polymerases, especially the hepatitis C virus (HCV) polymerase enzyme

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patent: 5420129 (1995-05-01), Breu et al.
patent: 6436943 (2002-08-01), Stoltefuss et al.
patent: WO 92/05159 (1992-04-01), None
patent: 19817265 (1998-04-01), None
patent: WO 00/13708 (2000-03-01), None
Roberts et al. “Basic principles of Organic Chemistry” (Benjamin, INC 1964) p. 531.
Methyl 2-(4-chlorophenyl)-5,6-dihydroxyprimidine-4-carboxylate, 1999 Maybridge plc catalog.
T. P. Culbertson, “Synthesis of 5,6-Dihydroxy-2-phenyl-4-pyrimidinecarbxylic Acid, Methyl Ester, a Corrected Structure,” J. Heterocyclic Chem., 1979, vol. 16, pp. 1423-1424.
A. A. Santilli et al., “Synthesis of 1,2,4-Oxadiazines and Their Rearrangement to Pyrimidines”, J. Heterocyclic Chem., 1979, vol. 16, pp. 213-216.
Translation of Claims of WO 92/05159.

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