Affiliation:
1. School of Chemistry College of Science University of Tehran Tehran Iran
2. Endocrinology and Metabolism Research Center Endocrinology and Metabolism Clinical Sciences Institute Tehran University of Medical Sciences Tehran Iran
3. Department of Biotechnology Faculty of Science Bartin University 74100- Bartin Turkey
Abstract
AbstractThis study reported an efficient two‐step method based on the sequential post‐Ugi hydroamination reaction for synthesizing a novel class of benzimidazole‐pyrazines with high yields. First, a Ugi fourcomponent reaction (Ugi‐4CR) is carried out using readily available starting materials, i. e., 1H‐benzo[d]imidazole‐2‐carboxylic acid, aldehydes, propargylamine, and isocyanides, in methanol at ambient temperature. Afterward, the Ugi products undergoes a sequential intramolecular hydroamination/cyclization reaction between a nitrogen of imidazole and alkyne functional group in aqua media in the presence of AuCl3 as a catalyst to obtain benzimidazole‐pyrazine products. These heterocyclic compounds may have a potential to be utilized in designing modern drugs with desirable features.