Heterocycles [h]-Fused onto 4-Oxoquinoline-3-carboxylic Acid, III. Facile Synthesis and Antitumor Activity of Model Heterocycles [a]-Fused onto Pyrido[2,3-f]quinoxaline-3-carboxylic Acids

Direct interaction between 7-chloro-1-cyclopropyl-6-fluoro-8-nitro-4oxo-1,4-dihydroquinoline-3-carboxylic acid and each of (S)-proline, (2S,4R)-4hydroxyproline and (S)-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid in hot aqueous ethanolic NaHCO 3 yielded the corresponding optically pure N-(4-oxoquinolin-7-yl)-α-amino acids.The latter derivatives underwent reductive lactamization upon treatment with Na 2 S 2 O 4 in aqueous ethanol to afford moderate yields of the respective pyrido[2,3-f]quinoxaline-3-carboxylic acid [fused]-to tetrahydropyrrolo[1,2-a]-, tetrahydrohydroxylpyrrolo[1,2-a]-and tetrahydroisoquinolino[2,3-a]heterocyclics 10-12, respectively.The antitumor activity against four human tumor cell lines showed that 10-12 displayed high levels of cytotoxicity as compared with Cisplatin.Interestingly, these compounds were more potent against breast carcinoma cell lines (MCF-7 and T-47D) than the lymphoid origin tumor cell lines (Jurkat and BHL-89).In particular, the (S)-proline derivative 10 exhibited preferential cytotoxicity to adherent cells (IC 50 = 0.5 µM), indicative of better potential in blocking the growth of solid tumors rather than the disseminated ones.