Synthesis of Novel Substituted Bis(benzimidazole)amine, N-Benzimidazole (benzothiazole)amine, and N-Benzimidazole(benzoxazole)amine Under Ultrasound Irradiation via Copper-Catalyzed Reaction

In this work, novel bis(benzimidazole)amine, N-benzimidazole(benzothiazole)amine, and N-benzimidazole(benzoxazole)amine have been synthesized via a one-pot, intramolecular cyclization of 2-iodoaniline and 2-aminobenzimidazoles (thiazoles and oxazoles)-trichloroacetonitrile adduct using copper(I) iodide and DMF under ultrasound-assisted reaction with moderate to good yields. Using basic materials and simple and available reagents, gentle copper-catalyzed reaction conditions, easy purification with the help of solvent, good yields, non-addition of ligands, application of a simple and efficient sonochemical method, short reaction times, and the synthesis of 15 new heterocycle compounds have been appreciable features of this protocol.

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Journal
Letters in Organic Chemistry
Published
2025-02-18
DOI
https://doi.org/10.2174/0115701786365139250130094121
Primary Topic
Synthesis and biological activity
Type
article
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article

Synthesis of Novel Substituted Bis(benzimidazole)amine, N-Benzimidazole (benzothiazole)amine, and N-Benzimidazole(benzoxazole)amine Under Ultrasound Irradiation via Copper-Catalyzed Reaction

Manijeh Nematpour
2 links
Letters in Organic Chemistry
Synthesis and biological activity
article

Synthesis of Novel Substituted Bis(benzimidazole)amine, N-Benzimidazole (benzothiazole)amine, and N-Benzimidazole(benzoxazole)amine Under Ultrasound Irradiation via Copper-Catalyzed Reaction

Manijeh Nematpour
article en

Abstract

In this work, novel bis(benzimidazole)amine, N-benzimidazole(benzothiazole)amine, and N-benzimidazole(benzoxazole)amine have been synthesized via a one-pot, intramolecular cyclization of 2-iodoaniline and 2-aminobenzimidazoles (thiazoles and oxazoles)-trichloroacetonitrile adduct using copper(I) iodide and DMF under ultrasound-assisted reaction with moderate to good yields. Using basic materials and simple and available reagents, gentle copper-catalyzed reaction conditions, easy purification with the help of solvent, good yields, non-addition of ligands, application of a simple and efficient sonochemical method, short reaction times, and the synthesis of 15 new heterocycle compounds have been appreciable features of this protocol.

Letters in Organic ChemistryVol. 22(9)
Farhangian University (IR)
Openalex Percentile: Top 98%
Synthesis and biological activity
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