An efficient synthesis and cytotoxic activity of 2‐(4‐chlorophenyl)‐1H–benzo[d]imidazole obtained using a magnetically recyclable Fe3O4 nanocatalyst‐mediated white tea extract

A simple and efficient procedure has been developed for the synthesis of biologically relevant 2‐substituted benzimidazoles through a one‐pot condensation of o‐phenylenediamines with aryl aldehydes catalysed by iron oxide magnetic nanoparticles (Fe3O4 MNPs) in short reaction times with excellent yields. In the present study, Fe3O4 MNPs synthesized in a green manner using aqueous extract of white tea (Camelia sinensis) (Wt‐Fe3O4 MNPs) were applied as a magnetically separable heterogeneous nanocatalyst to synthesize 2‐(4‐chlorophenyl)‐1H–benzo[d]imidazole which has potential application in pharmacology and biological systems. Fourier transform infrared and NMR spectroscopies were used to characterize the 2‐(4‐chlorophenyl)‐1H–benzo[d]imidazole. In vitro cytotoxicity studies on MOLT‐4 cells showed a dose‐dependent toxicity with non‐toxic effect of 2‐(4‐chlorophenyl)‐1H–benzo[d]imidazole, up to a concentration of 0.147 µM. The green synthesized Wt‐Fe3O4 MNPs as recyclable nanocatalyst could be used for further research on the synthesis of therapeutic materials, particularly in nanomedicine, to assist in the treatment of cancer. In this research, the green synthesized Fe3O4 MNPs using aqueous extract of white tea has been applied as magnetically separable heterogeneous nanocatalyst to synthesize 2‐(4‐Chlorophenyl)‐1 H benzo [d] imidazole which has potential application in pharmacology and biological systems. The present study successfully demonstrated a simple, eco‐friendly method for the imidaozol with significant potential anticancer properties.