Abstract

The 2‐amino‐7‐methoxypyrimido[4,5‐b]quinoline (1) on treatment with bis(methylthio)methylene malononitrile (2) in ethyl alcohol and catalytic amount of TEA gives 3‐cyano‐4‐imino‐9‐methoxy‐2‐methythio‐4H‐pyrimido[2,1‐b]pyrimido[4,5‐b]quinoline (3). The latter were further reacted with selected N‐, O‐, and C‐nucleophiles such as aryl amines, hetryl amines, substituted phenols, and compounds containing an active methylene group.

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