Nucleotide analogs
AssigneeGilead Sciences, Inc.
InventorsMurty N. Arimilli, Norbert W. Bischofberger, Robert J. Jones, William A. Lee, Ernest J. Prisbe
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Abstract
Nucleotide phosphonate esters characterized by the presence of an ester linked group which is bonded to the phosphorus atom of phosphonate nucleotide analogs are disclosed. The analogs comprise an ester bond that is hydrolyzed in vivo to yield a corresponding phosphonate nucleotide analog. Methods and intermediates for their synthesis and use are described.
Claims1
A compound having the structure of formula (1) ##STR36## wherein B is 5-fluorocytosin-1-yl, 5-methylcytosin-1-yl, or a heterocyclic base having the structure (a) ##STR37## R is --S(O).sub.2 N(R.sup.3).sub.2 ;
- each R.sup.1 is independently hydrogen, cyano, nitro, alkyl, O-alkyl, --C(O)R.sup.3, --S(O).sub.2 OH, --N(R.sup.3).sub.2 or --CHO;
- each R.sup.3 is independently hydrogen, alkyl, phenyl, phenyl substituted with C.sub.1-20 alkyl, --CH.sub.2 C.sub.6 H.sub.5 or --CH.sub.2 CH.sub.2 C.sub.6 H.sub.5, but when R.sup.1 is --N(R.sup.3).sub.2, one R.sup.3 is hydrogen and the other R.sup.3 is C.sub.2-6 alkyl or when R.sup.1 is --N(R.sup.3).sub.2, both R.sup.3 are the same and are C.sub.2-6 alkyl;
- R.sup.6 is --NH.sub.2, --NHR.sup.7, --NHR.sup.8, --N.dbd.CHN(R.sup.7).sub.2 or --N.dbd.C(CH.sub.3)N(R.sup.7).sub.2 ;
- R.sup.7 is C.sub.1 -C.sub.6 alkyl;
- R.sup.8 is a protecting group;
- and
- each R.sup.9 independently is N or CH.
Dependencies are inferred from the claim text.