Studies of Nucleosides and Nucleotides. XXXIX.1) Synthesis of 8-Substituted Purine Nucleotides by the Direct Replacement Reactions

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Abstract

8-Bromo-AMP and 8-bromo-GMP, which are key intermediate for the synthesis of 8-substituted purine nucleotides, were synthesized directly from AMP and GMP by the bromination with bromine-water in buffer solution. 8-Bromo-MP's were converted to 8-oxy compounds by the reaction with sodium acetate in acetic anhydride or in acetic acid. 8-Dimethylamino-GMP was obtained by replacement of 8-bromo-atom with dimethyl-amine. These 8-substituted purine nucleoside monophosphates were derived to 5′-diphosphates via phosphoromorpholidate. A convenient synthesis of [α-32P]-8-bromo-ADP was described. © 1969, The Pharmaceutical Society of Japan. All rights reserved.

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Ikehara, M., Tazawa, I., & Fukui, T. (1969). Studies of Nucleosides and Nucleotides. XXXIX.1) Synthesis of 8-Substituted Purine Nucleotides by the Direct Replacement Reactions. Chemical and Pharmaceutical Bulletin, 17(5), 1019–1024. https://doi.org/10.1248/cpb.17.1019

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