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Mendeleev Communications, 2024, Volume 34, Issue 2, Pages 279–281
DOI: https://doi.org/10.1016/j.mencom.2024.02.039
(Mi mendc108)
 

Communications

Unexpected transamination between 2-aminoazoles and N-iodoacetyl azoles

N. O. Yarosh, I. A. Dorofeev, L. V. Zhilitskaya, B. A. Shainyan

A.E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, Irkutsk, Russian Federation
Abstract: N-Iodoacetyl-substituted azoles undergo transfer of iodoacetyl group from heterocyclic N atom toward the amino group of amino azoles, unlike the earlier investigated iodomethyl ketones. The proposed mechanism explaining the observed difference in such transamination is confirmed by calculations. The product derived from 2-aminobenzimidazole is cyclized into fused imidazo[1,2-α]benzimidazol- 9-ium salt.
Keywords: aminoazoles, iodoacetyl azoles, transamination, cyclization, imidazo[1,2-a]benzimidazol-9-ium salts, quantum chemical calculations.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (1.2 Mb)


Citation: N. O. Yarosh, I. A. Dorofeev, L. V. Zhilitskaya, B. A. Shainyan, “Unexpected transamination between 2-aminoazoles and N-iodoacetyl azoles”, Mendeleev Commun., 34:2 (2024), 279–281
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