Hydrolysis of the prodrug, 2',3',5'-triacetyl-6-azauridine.

C M Riley, M A Mummert, J Zhou, R L Schowen, D G Vander Velde, M D Morton, M Slavik

Index: Pharm. Res. 12(9) , 1361-70, (1995)

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Abstract

The purposes were to study the kinetics of hydrolysis of 2',3',5'-triacetyl-6-azauridine (1) in aqueous solution (mu = 0.5) and to identify the main intermediates and products of the reaction.A stability indicating isocratic LC assay was used to study the rate of degradation of 1. A gradient LC assay was used to study the time courses of the degradants. The products of hydrolysis were isolated by preparative liquid chromatography and identified by 1H-NMR and CI-MS. The pKa value was obtained by potentiometric titration.At 36.8 degrees C, the pH-rate profile of 1 in water was adequately described by a four-term rate equation. The intermediates were identified as the primary and secondary di-acetates, and the primary and secondary mono-acetates. The final product was 6-azauridine.A simplified kinetic scheme could be used to describe the concentration-time profiles of 1, the intermediates and the final product.