94822-28-3Relevant academic research and scientific papers
I2-Mediated Intramolecular C-H Amidation for the Synthesis of N-Substituted Benzimidazoles
Hu, Zhiyuan,Zhao, Ting,Wang, Manman,Wu, Jie,Yu, Wenquan,Chang, Junbiao
, p. 3152 - 3158 (2017/03/23)
A practical intramolecular C-H amidation methodology has been developed using molecular iodine under basic conditions. The required imine substrates were readily obtained by condensation of simple o-phenylenediamine derivatives and aldehydes. The transition-metal-free cyclization reaction described here works well with crude imines and allows for the sequential synthesis of N-protected benzimidazoles without purification of the less stable condensation intermediates. This operationally simple synthetic approach is broadly applicable to a variety of aromatic, aliphatic, and cinnamic aldehydes to produce diverse 1,2-disubstituted benzimidazole derivatives in an efficient and scalable fashion.
Benzazoles. 3*. Synthesis and arylsulfonylation of 2-substituted benzimidazoles
Abdireimov,Mukhamedov,Aiymbetov,Shakhidoyatov
, p. 941 - 946 (2011/09/20)
2-Alkylbenzimidazoles have been obtained from o-nitroaniline and aliphatic carboxylic acids by reductive cyclization. Interaction of the former with arenesulfonyl chlorides led to the synthesis of 2-alkyl-1- arylsulfonylbenzimidazoles, the yield of which depended on the structure of the substituent in position 2.
