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A facile synthesis of annulated azolo[c][1,2,4]thiadiazine S,S-dioxides

Tetrahedron Lett. , 2013, 54 (8), 986-988

DOI: 10.1016/j.tetlet.2012.12.040

Cherepakha A.; Kovtunenko V. O.; Tolmachev A.

Condensations of o-halo-substituted benzenesulfonyl chlorides with 3-aminoazoles give the corresponding azolo[c][1,2,4]benzothiadiazine S,S-dioxides. o-Fluorobenzenesulfonyl chlorides and o-bromobenzenesulfonyl chlorides bearing a nitro group are reactive enough to give the desired azolo[c][1,2,4]benzothiadiazine S,S-dioxides in a one-pot, base-promoted reaction. In all other cases, open-chain sulfonylated 3-aminoazole intermediates are isolated. The latter are converted into the title compounds upon addition of a copper(I) catalyst.

A facile synthesis of annulated azolo[c][1,2,4]thiadiazine S,S-dioxides

Cherepakha A.; Kovtunenko V. O.; Tolmachev A.
Tetrahedron Lett. 2013, 54 (8), 986-988
DOI: 10.1016/j.tetlet.2012.12.040

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