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Synthesis of acyclic nucleoside phosphonates as antiviral compounds
Authors:Frank Wormstdt  Michael Gütschow  Kurt Eger  Ute Brinckmann
Institution:Frank Wormstädt,Michael Gütschow,Kurt Eger,Ute Brinckmann
Abstract:Reaction of 6‐chloropyrimidines with diethyl (2‐aminoethoxy)methyl]phosphonate allows for a ready access to acyclic nucleoside phosphonates. A series of 5‐substituted pyrimidines bearing a phosphonate side chain at position 6 were synthesized and tested against herpes simplex viruses (HSV‐1 and HSV‐2) and human immunodeficiency virus (HIV‐1). Some compounds showed weak antiviral activity against HSV‐1.
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