A series of new piperizine-quinoline derivatives (RB1-10) were designed and synthesized from 4- (bromomethyl)quinolin-2(1H)-one and arylpiperazines. The structure of newly synthesized compounds were characterized by spectral data’s and screened for their cytotoxic activity against barest cancer cell lines. The compound RB1 with trifluoromethoxy substitution on aryl group showed moderate activity.
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