Syntheses of Some Benzimidazoles from N-Arylamidines
Motoi OHOSONE, Shigeo Tanimoto, Ryohei Oda
Abstract
Open-access reader
Motoi OHOSONE, Shigeo Tanimoto, Ryohei Oda
Abstract
Open-access reader
Grenda's method to convert arylamidine hydrochloride into benzimidazole with the aid of sodium hypochloride and a base has been applied to the previously untried N-arylamidines to synthesize the following : 5-chloro-2-phenylbenzimidazole (Y=96%), 5-methyl-2-phenylbenzimidazole (Y=96%), 2-benzylbenzimidazole (Y=50%), 2-benzyl-5-chlorobenzimidazole (Y=70%), 2-(2'-naphthyl)-benzimidazole (Y=75%), 5-chloro-2-(2'-naphthyl)-benzimidazole (Y=90%), 2-(p-tolyl)-benzimidazole (Y=95%), 5-chloro-2-(p-tolyl)-benzimidazole (Y=80%), 5-methyl-2-(p-tolyl)-benzimidazole (Y=80%).
OpenAlex reports 5 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Grenda's method to convert arylamidine hydrochloride into benzimidazole with the aid of sodium hypochloride and a base has been applied to the previously untried N-arylamidines to synthesize the following : 5-chloro-2-phenylbenzimidazole (Y=96%), 5-methyl-2-phenylbenzimidazole (Y=96%), 2-benzylbenzimidazole (Y=50%), 2-benzyl-5-chlorobenzimidazole (Y=70%), 2-(2'-naphthyl)-benzimidazole (Y=75%), 5-chloro-2-(2'-naphthyl)-benzimidazole (Y=90%), 2-(p-tolyl)-benzimidazole (Y=95%), 5-chloro-2-(p-tolyl)-benzimidazole (Y=80%), 5-methyl-2-(p-tolyl)-benzimidazole (Y=80%).
Key concepts: Benzimidazole, Chemistry, Hydrochloride, Sodium, Medicinal chemistry, Organic chemistry