Abstract:
2,6-Di-tert-butyl-4-{[2-(2-aryl-2-oxoethylthio)-1H-imidazol-1-yl]imino}cyclohexa-2,5-dien-1-ones under the action of bases give products of the 2,3-dihydroimidazo[2,1-b]thiazol- 3-ol series by subsequent recyclization reaction of the intermediate imidazo[2,1-b][1,3,4]thiadiazoles. The structure of imidazo[2,1-b]thiazol-3-ol is supported by the X-ray diffraction. The features of the cyclization processes of quinone imine derivatives were stimulated by DFT calculations using the wB97XD/6-311++G** method.
Citation:
A. A. Kolodina, D. V. Steglenko, E. S. Khodykina, N. I. Gaponenko, M. S. Galkina, O. P. Demidov, A. V. Metelitsa, “Unusual cyclization of N-imidazolyl quinone imines with the formation of thiadiazole ring and its subsequent recyclization”, Mendeleev Commun., 32:3 (2022), 386–389
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https://www.mathnet.ru/eng/mendc673
https://www.mathnet.ru/eng/mendc/v32/i3/p386
This publication is cited in the following 1 articles:
Evgenia S. Khodykina, Dmitry V. Steglenko, Elena V. Vetrova, Artem D. Pugachev, Maria S. Galkina, Inna G. Borodkina, Alexander V. Lesin, Oleg P. Demidov, Anatoly V. Metelitsa, Alexandra A. Kolodina, “Intramolecular Cyclization of the ortho‐Substituted N‐arylquinone Imines under Basic and Thermal Conditions”, ChemistrySelect, 8:3 (2023)