The synthesis and anticancer activity of a series of new 3-amido derivatives of 3-chloro-10H-pyrido[3,2-b][1,4]benzoxazine and 3-chloro-10H-pyrido[3,2-b][1,4]benzothiazine is presented. The synthesized structures were characterized by UV-visible, FT-IR, 1H NMR spectroscopy and elemental analytical data. The in silico physicochemical properties disclosed that neither 3-chloro-10H-pyrido[3,2-b][1,4]benzoxazine and 3-chloro-10H-pyrido[3,2-b][1,4]benzothiazine intermediates nor their carboxyamido derivatives violate Lipinski’s rule of five. In addition, molecular docking studies showed that they exhibited good interaction with cancer receptors. 1,3-di-10H-Pyrido[3,2-b][1,4]benzothiazin-3-ylurea which showed a significant interaction with all the employed receptors possessed the highest anticancer activity.
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