Nucleosides. Part IX. Direct synthesis of uracil nucleosides

Journal of the Chemical Society C: Organic Pub Date: DOI: 10.1039/J39690002450

Abstract

The direct synthesis of uracil nucleosides results from the reaction of uracil with a glycosyl halide in the presence of mercuric cyanide. In this way, uracil can be converted into N(3)-(2′,3′,4′,6′-tetra-O-acetyl-β-D-glucopyranosyl)uracil (I) and N(1)N(3)-bis-(2′,3′,4′,6′-tetra-O-acetyl-β-D-glucopyranosyl)uracil (III). Either (I) or (III) can be obtained as the main product in high yield by choice of appropriate reaction conditions; (III) is formed from (I)via the N(3)O(6)-bisglucoside (II). A convenient synthesis of 2′,3′,5′-tri-O-acetyluridine illustrates the usefulness of the method.

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