《Solvent-mediated Highly Efficient Synthesis of [1,2,4]triazolo/benzimidazoloquinazolinone Derivatives》 was written by Malamiri, Fatemeh; Khaksar, Samad; Badri, Rashid; Tahanpesar, Elham. Safety of 1H-Benzo[d]imidazol-2-amineThis research focused ontriazoloquinazolinone preparation; aminotriazole dimedone benzaldehyde cyclocondensation trifluoroethanol mediated; benzimidazoloquinazolinone preparation; aminobenzimidazole dimedone benzaldehyde cyclocondensation trifluoroethanol mediated; Fluorinated alcohols; anticancer; green chemistry; heterocyclic; multicomponent; triazole. The article conveys some information:
An efficient and catalyst-free procedure for the synthesis of triazoloquinazolinones I [Ar = Ph, 4-MeC6H4, 2,4-di-ClC6H3, etc.] and benzimidazoloquinazolinones II [R = Ph, 4-ClC6H4, 4-O2NC6H4, etc.] was developed in 2,2,2-trifluoroethanol or deep eutectic solvent(DESs) as a clean and reusable media. Various products were obtained in good to excellent yields under reaction conditions. The results came from multiple reactions, including the reaction of 1H-Benzo[d]imidazol-2-amine(cas: 934-32-7Safety of 1H-Benzo[d]imidazol-2-amine)
1H-Benzo[d]imidazol-2-amine(cas: 934-32-7) can be used in the hydrolysis of a choline carbonate. It was also used in the synthesis of imidazo[1,2-a]benzimidazoles.Safety of 1H-Benzo[d]imidazol-2-amine
Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem