AN UNEXPECTED SYNTHESIS OF β-AMINO-α-MESYL-γ-SULTAMS UPON MESYLATION OF HINDERED α-AMINONITRILES
DOI:
https://doi.org/10.1007/5476Ключевые слова:
aminonitriles, spiro compounds, sulfonamides, cyclization, X-ray studyАннотация
We report one-pot procedure for an unexpected synthesis of previously unknown 4-amino-5-methylsulfonyl-2,3-dihydroisothiazole 1,1-dioxides (also called β-amino-α-mesyl-γ-sultams). Thus, the reaction of mesyl chloride with hindered α-aminonitriles is accompanied by the formation of interim N-(1-cyanoalkyl)(methylsulfonyl)methanesulfonamides which, in turn, undergo the сarbanion-mediated sulfonate (sulfonamido) intramolecular cyclization reaction yielding β-amino-α-mesyl-γ-sultams. The structure of the title compounds was confirmed by X-ray diffraction study. The proposed mechanistic insights of the reaction are in accordance with the results of additional experiments and literature data.Загрузки
Опубликован
2020-04-01
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Оригинальные статьи