Abstract
Synthesis and preliminary biological evaluation of imidazo (2, 1-b) Thiazole
derivatives is reported. Under Mannich conditions, a series of new imidazo (2, 1-b)
Thiazole derivatives were synthesized. Starting from the reaction of 2- amino
thiazole with 4- bromo phenyl bromide to produce 5-(4-bromo phenyl) imidazo (2,
1-b) thiazoles, following by introduce the substituted aminomethyl at position 6-by
reacting with different aromatic amines under Mannich conditions to afford 6-
secondary amine-5-(4-bromo phenyl) imidazo (2,1-b) thiazole in high yields.
FT-IR, 1H NMR, and 13C NMR techniques were used to characterize the
synthesized derivatives. In addition, all compounds were tested for their antioxidant
activity, and three of them were examined for cytotoxic activity against kidney
cancer using an MTT assay. The product (A9) has shown an excellent anti-cancer
activity with 69.69 value.
derivatives is reported. Under Mannich conditions, a series of new imidazo (2, 1-b)
Thiazole derivatives were synthesized. Starting from the reaction of 2- amino
thiazole with 4- bromo phenyl bromide to produce 5-(4-bromo phenyl) imidazo (2,
1-b) thiazoles, following by introduce the substituted aminomethyl at position 6-by
reacting with different aromatic amines under Mannich conditions to afford 6-
secondary amine-5-(4-bromo phenyl) imidazo (2,1-b) thiazole in high yields.
FT-IR, 1H NMR, and 13C NMR techniques were used to characterize the
synthesized derivatives. In addition, all compounds were tested for their antioxidant
activity, and three of them were examined for cytotoxic activity against kidney
cancer using an MTT assay. The product (A9) has shown an excellent anti-cancer
activity with 69.69 value.
Keywords
1-B) Thiazole Moiety
Anti-cancer and Antioxidant Activities of Some New Synthesized Mannich Bases Containing an Imidazo (2