Photodecomposition of a new 1,4‐dihydropyridine: Furnidipine
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Núñez Vergara, Luis
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Photodecomposition of a new 1,4‐dihydropyridine: Furnidipine
Abstract
The photodecomposition of new 1,4‐dihydropyridine, furnidipine (CRE‐319); 2,6‐dimethyl‐4‐(2‐nitrophenyl)‐1,4‐dihydropy‐ridine‐3,5‐dicarboxylic acid 3‐tetrahydrofurfuryl (5‐methyl diester) was studied by voltammetric, UV‐vis spectrophotometric, and HPLC technique with three different light conditions (artificial daylight, UV light, and room daylight). The artificial daylight photodecomposition of furnidipine follows 0.5‐order kinetics as assessed by the abovementioned techniques. Furthermore, the daylight photoderivative was isolated and identified by NMR and IR as 2,6‐dimethyl‐4‐(2‐nitrosophenyl)pyridine‐3,5‐dicarboxylic acid 3‐tetrahydrofurfuryl 5‐methyl diester. Quantitative kinetic data for the UV photodecomposition of furnidipine cannot be obtained due to both the high rate of degradation (<1 min) and intermediate reactions. However, polarographic, spectroscopic, and chromatographic evidence permits us to identify this photoproduct as 2,6‐dimethyl‐4‐(2‐nitrophenyl)pyridine‐3,5‐dica
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URI: https://repositorio.uchile.cl/handle/2250/156541
DOI: 10.1002/jps.2600830412
ISSN: 15206017
00223549
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Journal of Pharmaceutical Sciences, Volumen 83, Issue 4, 2018, Pages 502-507
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