Issue 42, 2018

Electrophilic halogenation of hydrazones of CF3-ynones. Regioselective synthesis of 4-halo-substituted 3-CF3-pyrazoles

Abstract

An efficient approach for the synthesis of 4-halo-3-CF3-pyrazoles was elaborated using the cyclization of hydrazones of CF3-ynones induced by electrophilic halogenation. This method can be used for the regioselective synthesis of 3-CF3-pyrazoles substituted at the 4-position with any halogen (I, Br or Cl). The high (up to quantitative) yields, mild conditions and simplicity of the reaction protocol are the advantages of the proposed method. It was demonstrated that cross-coupling with 4-iodo-3-CF3-pyrazoles can be used for the synthesis of a broad family of tetrasubstituted pyrazoles. Moreover, it was found that this method is suitable for the synthesis of 4-substituted derivatives of Celebrex and SC-560.

Graphical abstract: Electrophilic halogenation of hydrazones of CF3-ynones. Regioselective synthesis of 4-halo-substituted 3-CF3-pyrazoles

Supplementary files

Article information

Article type
Paper
Submitted
11 Sep 2018
Accepted
28 Sep 2018
First published
28 Sep 2018

Org. Biomol. Chem., 2018,16, 7935-7946

Electrophilic halogenation of hydrazones of CF3-ynones. Regioselective synthesis of 4-halo-substituted 3-CF3-pyrazoles

V. M. Muzalevskiy and V. G. Nenajdenko, Org. Biomol. Chem., 2018, 16, 7935 DOI: 10.1039/C8OB02247J

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