Abstract
In this work, the multi-step synthesis and characterization of novel 2-(3-methoxy-9H-carbazol-9-yl)-N-phenyl acetamide analogues is presented. These analogues were synthesized from 2-(3-methoxy-9H-carbzol-9-yl)acetyl chloride with substituted aromatic primary amines in the presence of organic base such as triethylamine and methylene dichloride under reflux conditions. The elemental analysis and structures of these novel compounds were elucidated by analyzing spectral data obtained through 1H NMR, 13C NMR and LCMS techniques. The bioevaluation of these newly synthesized compounds has been studied by evaluating their antibacterial and antifungal activities against various kinds of bacterial and fungal strains, respectively.
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