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A practical method, NaOCl-mediated, to prepare thiabendazoles via intramolecular amination reaction
Journal article   Peer reviewed

A practical method, NaOCl-mediated, to prepare thiabendazoles via intramolecular amination reaction

Vikrant Patil, Enrique Barragan, Shivaputra A Patil, Siddappa A Patil and Alejandro Bugarin
Tetrahedron letters, Vol.58(35), pp.3474-3477
08-30-2017

Abstract

Bleach Characterization Single-crystal X-ray diffraction Synthesis Thiabendazole
[Display omitted] •A practical method for the synthesize several thiabendazole derivatives.•A metal-free protocol is documented.•Good functional group tolerance.•Easy access to structurally complex heterocycles.•Fully characterized adducts are reported. A series of new chlorinated thiabendazoles (6a–m) have been synthesized from readily available anilines and 4-cyanothiazole in moderate to good yields. All synthesized compounds were fully characterized using 1H NMR, 13C NMR, IR, and mass spectrometry. Additionally, the structure of the compound (6f) was confirmed by single-crystal X-ray diffraction. In addition, synthesis of 2-substituted benzimidazoles and 2-phenyl benzothiazole was investigated using our optimized conditions and the outcome is presented herein.

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