Chemistry & Biodiversity 2004-01-01

One-step synthesis of hypoxanthine from glycinamide and diformylurea.

Irene M Lagoja, Piet Herdewijn

Index: Chem. Biodivers. 1(1) , 106-11, (2004)

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Abstract

Because of their easy availability and their relative chemical stability, urea, formic acid, and glycine might have played a role in the assembly process of nucleobases. In this paper, a short reaction path is described to prepare hypoxanthine starting from the above mentioned precursors. The formation of hypoxanthine has been verified by high-resolution mass spectrometry with the 15N-labelled urea as starting material, and HPLC analysis. The yield of this condensation reaction has been determined spectrophotometrically.

Related Compounds

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H-Gly-NH2.HCl Structure H-Gly-NH2.HCl
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