Effect of the 6-Methyl Group on Peroxyl Radical Trapping by 5-Hydroxyand 5-Amino- Derivatives of 1,3-Dimethyluracil

Title:Effect of the 6-Methyl Group on Peroxyl Radical Trapping by 5-Hydroxyand 5-Amino- Derivatives of 1,3-Dimethyluracil

Volume: 14 Issue: 1

Author(s): Stanislav A. Grabovskiy*, Arcadiy V. Antipin, Yulia S. Grabovskaya, Nadezhda M. Andriayshina, Oksana V. Akchurina and Natalie N. Kabal`nova

Affiliation:

• Ufa Institute Chemistry of the Russian Academy of Sciences, Ufa, Russian Federation, Russia,Russian Federation

Keywords: DFT, inhibition, kinetics, oxidation, peroxyl radical, pyrimidinones.

Abstract: Background: Many synthetic and natural uracil derivatives have biological activity. Furthermore, many of these derivatives have pro- and antioxidant properties, but the mechanism of these processes is far from being understood.

Methods: Oxygen-uptake kinetics and computational methods (CBS-QB3, M062X/MG3S and SMDM05/ MG3S) were combined to study the reaction of peroxyl radicals with five organic-soluble derivatives: 5-amino- and 5-hydroxy-1,3-dimethyluracil, 5-amino- and 5-hydroxy-1,3,6-trimethyluracil, and 5-hydroxy-1,3-dimethyl-6-phenyluracil in chlorobenzene.

Results: The studied uracil derivatives should be classified as inhibitors of medium reactivity kin = (1-10) × 10-4 M-1 s-1. The methyl group in the 6-position of the pyrimidine ring increases the rate constant of the reaction with peroxyl radicals by 3-4 times and the stoichiometric coefficient of inhibition. The calculation of the reaction barrier heights at the SMD-M05/MG3S level of theory for the hydrogen abstraction is in good agreement with experimental data.

Conclusion: 1,3-Dimethyl-5-aminouracil is transformed by the addition of a methyl group at the 6-position into a favic-like pyrimidine, while the 5-hydroxy derivative becomes a more effective antioxidant. The bound dissociation energy (O-H or N-H) and the IP for the reactivity forecasting of uracil derivatives were used, but it was found that this methodology did not lead to good correlation between experimental and theoretical results. The SMD-M05/MG3S method provided the most accurate calculations of the reaction barrier heights for hydrogen abstraction from uracil derivatives by peroxyl radical.

Cite this article as:

Grabovskiy A. Stanislav *, Antipin V. Arcadiy , Grabovskaya S. Yulia , Andriayshina M. Nadezhda , Akchurina V. Oksana and Kabal`nova N. Natalie , Effect of the 6-Methyl Group on Peroxyl Radical Trapping by 5-Hydroxyand 5-Amino- Derivatives of 1,3-Dimethyluracil, Letters in Organic Chemistry 2017; 14 (1) . https://dx.doi.org/10.2174/1570178614666161121123024

DOI https://dx.doi.org/10.2174/1570178614666161121123024	Print ISSN 1570-1786
Publisher Name Bentham Science Publisher	Online ISSN 1875-6255