Abstract
α-(5-Nitrofuryl-2) quinoxaline, and its α′-cyano- and α′-oxyderivative were synthesized by nitration of the respective furylquinoxalines with a nitrating mixture. When 2-oxy-3-(furyl-2) quinoxaline is subjected to nitration with excess of nitric acid a dinitro-derivative is formed which is presumably 6-nitro-3-(5-nitrofuryl-2)-2-oxyquinoxaline. The antibacterial, tuberculostatic, and fungistatic activities of the α-(furyl-2)- and α-(5-nitrofuryl-2) quinoxalines and their derivatives were studied “in vitro.”
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