A simple and convenient procedure was adopted for the synthesis of N-(3-acridin-9-yl-4-chloro/hydroxy-phenyl-alkyl)-arylamides/imides starting from 5-(arylamido/imido-alkyl)-2-chloro/2-hydroxy benzoic acids. The compounds were obtained in the yields ranging from 40 to 45% and exhibited less pronounced antiviral activity.
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