2006Synthetic CommunicationsRequires access

Regioselective N‐Arylation of Some Pyrimidine and Purine Nucleobases

Ali Khalafi‐Nezhad, Abdolkarim Zare, Abolfath Parhami, Mohammad Navid Soltani Rad, Gholam‐Reza Nejabat

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Abstract

N‐Arylation of some pyrimidine and purine nucleobases in the presence of SiO2 and Cs2CO3 under solvent‐free as well as in solution conditions is described. In these conditions, N1‐aryl pyrimidines and N9‐aryl purines have been obtained regioselectively in moderate to high yields with relatively short reaction times.

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What this paper is about

N‐Arylation of some pyrimidine and purine nucleobases in the presence of SiO2 and Cs2CO3 under solvent‐free as well as in solution conditions is described. In these conditions, N1‐aryl pyrimidines and N9‐aryl purines have been obtained regioselectively in moderate to high yields with relatively short reaction times.

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Available abstract

N‐Arylation of some pyrimidine and purine nucleobases in the presence of SiO2 and Cs2CO3 under solvent‐free as well as in solution conditions is described. In these conditions, N1‐aryl pyrimidines and N9‐aryl purines have been obtained regioselectively in moderate to high yields with relatively short reaction times.

Key concepts: Nucleobase, Chemistry, Pyrimidine, Purine, Purine metabolism, Regioselectivity, Aryl, Combinatorial chemistry

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