Material design and biologically activity of some new azetidines and azetidine-2-ones as antioxident

Abstract

The antioxidant activity of the produced compounds was tested in vitro. The DPPH radical scavenging activity of azetidinens and azetidine-2-ones seemed promising. The synthesis of azetidine derivatives is the focus of this research. With modest yields, these compounds were made by reacting alkyl halides with (imines) in ethanol at 70–60 °C (51–75 percent). Also, the response. The main focus of this research is on the synthesis and characterization of Imine compounds. These compounds are made by reacting an amine with an aldehyde or ketones in methanol and then adding drops of glacial acetic acid under reflux. The synthesis and characterisation of Azitidine-2-one 2 are also part of this research (A-). These chemicals are made by combining Schiff's bases with triethylamine and chloroacetyle chloride in the presence of triethylamine. Moderately administer the appropriate beta-lactams in dry dichloromethane withStir at 0 °C.