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Three-component synthesis of C2F5-substituted pyrazoles from C2F5CH2NH2•HCl, NaNO2 and electron-deficient alkynes

Beilstein J. Org. Chem. 2015, 11 16-24

DOI: 10.3762/bjoc.11.3

Mykhailiuk P. K.

A one-pot reaction between C2F5CH2NH2•HCl, NaNO2 and electron-deficient alkynes gives C2F5-substituted pyrazoles in excellent yields. The transformation smoothly proceeds in dichloromethane/water, tolerates the presence of air, and requires no purification of products by column chromatography. Mechanistically, C2F5CH2NH2•HCl and NaNO2 react first in water to generate C2F5CHN2, that participates in a [3 + 2] cycloaddition with electron-deficient alkynes in dichloromethane.

Three-component synthesis of C2F5-substituted pyrazoles from C2F5CH2NH2•HCl, NaNO2 and electron-deficient alkynes

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