Novel and Efficient Synthesis of Benzimidazole and Benzthiazole Moieties Mediated by Triflic Anhydride and 2-Nitropyridine

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Abstract

In the present report, inter and intramolecular C−N bond formation between the carbonyl carbon of urea or amide functional group with various amines mediated by triflic anhydride and 2-nitropyridine is successfully investigated for the first time. The versatility of the method is demonstrated by exploring it on a wide range of substrates to synthesize diversified 2-aminobenzimidazole, 2-aminopyridoimidazole and 2-substituted benzimidazole and benzthiazoles. Short reaction time, high yields and applicability in milder metal free reaction conditions are the highlights of the present methodology.

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Quadri, S. A. I., Das, T. C., & Farooqui, M. (2017). Novel and Efficient Synthesis of Benzimidazole and Benzthiazole Moieties Mediated by Triflic Anhydride and 2-Nitropyridine. ChemistrySelect, 2(5), 1802–1807. https://doi.org/10.1002/slct.201602049

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