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Copper-Promoted One-Pot Approach: Synthesis of Benzimidazoles

A facile, one-pot, and proficient method was developed for the production of various 2-arylaminobenzimidazoles. This methodology is based for the first time on a copper catalyst promoted domino C–N cross-coupling reaction for the generation of 2-arylaminobenzimidazoles. Mechanistic investigations re...

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Detalles Bibliográficos
Autores principales: Boddapati, S. N. Murthy, Tamminana, Ramana, Gollapudi, Ravi Kumar, Nurbasha, Sharmila, Assal, Mohamed E., Alduhaish, Osamah, Siddiqui, Mohammed Rafiq H., Bollikolla, Hari Babu, Adil, Syed Farooq
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7221555/
https://www.ncbi.nlm.nih.gov/pubmed/32295143
http://dx.doi.org/10.3390/molecules25081788
Descripción
Sumario:A facile, one-pot, and proficient method was developed for the production of various 2-arylaminobenzimidazoles. This methodology is based for the first time on a copper catalyst promoted domino C–N cross-coupling reaction for the generation of 2-arylaminobenzimidazoles. Mechanistic investigations revealed that the synthetic pathway involves a copper-based desulphurization/nucleophilic substitution and a subsequent domino intra and intermolecular C–N cross-coupling reactions. Some of the issues typically encountered during the synthesis of 2-arylaminobezimidazoles, including the use of expensive catalytic systems and the low reactivity of bromo precursors, were addressed using this newly developed copper-catalyzed method. The reaction procedure is simple, generally with excellent substrate tolerance, and provides good to high yields of the desired products.