5-Substituted-2, 4-diamino-6-[2-(phosphonomethoxy) ethoxy] pyrimidines Acyclic Nucleoside Phosphonate Analogues with Antiviral Activity

…, M Masojídková, G Andrei, R Snoeck…

Index: Hockova, Dana; Holy, Antonin; Masojidkova, Milena; Andrei, Graciela; Snoeck, Robert; De Clercq, Erik; Balzarini, Jan Journal of Medicinal Chemistry, 2003 , vol. 46, # 23 p. 5064 - 5073

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Citation Number: 89

Abstract

2, 4-Diamino-6-hydroxypyrimidines substituted in position 5 by an allyl, benzyl, cyanomethyl, ethoxycarbonylmethyl, phenyl, cyclopropyl, or methyl group were prepared either by C5- alkylation or by formation of the pyrimidine ring by cyclization. Their alkylation with 2-[( diisopropoxyphosphoryl) methoxy] ethyl tosylate afforded N1-and O6-regioisomers that were separated and converted to the free phosphonic acids by treatment with ...