Benzimidazole nucleus is one of the most important heterocycles exhibiting remarkable pharmacological activities. Numerous method for the synthesis of benzimidazole and also their diverse reactions offer enormous scope in the field of medicinal chemistry. Various reported biological activities (analgesic, anti-inflammatory, anthelmintic, anticancer, anthelmintic, antioxidant, antitubercular, an...

Ni2+ supported on hydroxyapatite-core@shell γ-Fe2O3 nanoparticles (γ-Fe2O3@HAp-Ni2+) was found to be a useful catalyst for the synthesis of benzimidazole derivatives from o-phenylenediamine and aldehydes under solvent and solvent-free conditions at 80 °C. This reaction affords the corresponding benzimidazole derivatives compared with the classical reactions this method consistently gives a high...

An efficient one-pot oxidation/condensation tandem process has been developed for the synthesis of 2-substituted benzimidazole derivatives from benzylic alcohols and 1,2-phenylenediamine with use of urea-hydrogen peroxide/silica phosphoric acid  as a bifunctional catalyst. This method provides a rapid and efficient access to 2-substituted benzimidazoles.

Benzimidazole and its derivatives are molecules that have diverse biological properties, therefore we synthesized studied a new benzimidazole to understand their physical/chemical properties. The compound was obtained through synthetic route, using graphite oxide, in the absence of solvent, with crystalline packaging supported by C–H…N C–H…π interactions. According frontier molecular orbitals, ...

Cancer is one of the most serious lifethreatening diseases for which there presently no cure. According to current World Health Organization (WHO) reports cancer responsible out every six deaths worldwide. Benzimidazole a heterocyclic, aromatic molecule that acts as biological scaffold with anticancer, antitumor, and antiproliferative activities, among other effects. benzimidazole oxazole are i...

ni2+ supported on hydroxyapatite-core@shell γ-fe2o3 nanoparticles (γ-fe2o3@hap-ni2+) was found to be a useful catalyst for the synthesis of benzimidazole derivatives from o-phenylenediamine and aldehydes under solvent and solvent-free conditions at 80 °c. this reaction affords the corresponding benzimidazole derivatives compared with the classical reactions this method consistently gives a high...

An efficient synthesis of the angiotensin II receptor antagonist Telmisartan (1) is presented involving a cross coupling of 4-formylphenylboronic acid 10 with 2-(2-bromophenyl)-4,4-dimethyl-2-oxazoline (11) as the key step (90% yield). The benzimidazole moiety 15 was constructed regioselectively via a reductive amination-condensation sequence, replacing the alkylation of the preformed benzimida...

Benzimidazole, which is a heterocyclic nucleus, plays an important role in various medicines. A number of therapeutic agents such as H1 antihistaminic agent clemizole, a potent opioid analgesic etonitazene, nonnucleoside antiviral compound enviroxime, for promotion of excretion of uric acid irtemazole, non sedating antihistaminic agent astemizole, anti ulcer drugs omeprazole and pentoprazole, a...

Boc-protected benzimidazole-pyrrole, benzimidazole-imidazole, and benzimidazole-methoxypyrrole amino acids were synthesized and incorporated into DNA binding polyamides, comprised of N-methyl pyrrole and N-methyl imidazole amino acids, by means of solid-phase synthesis on an oxime resin. These hairpin polyamides were designed to determine the DNA recognition profile of a side-by-side benzimidaz...

a one-pot multicomponent reaction of aryl aldehydes, 2-amino benzimidazole and ethyl 2-mercaptoacetate is described as an efficient and environmentally method for the synthesis of  some  novel  ethyl  2-((1h-benzo[d]imidazol-2-ylamino)(aryl)methylthio)  acetates  in  the presence of nano-copper y zeolite (ncz) as a catalyst in ethanol at room temperature. after optimizing of reaction conditions...