摘要:
N-(Vinyloxyalkyl)enaminoketones were obtained by the condensation of vinyloxyalkyl-amines with acetylacetone or ethyl acetoacetate. Their subsequent reactions with 1,4-benzoquinone produce the corresponding 5-hydroxy-2-methyl-N-(2-vinyloxyalkyl)indoles in 17-43% yields. The structures of the compounds obtained were confirmed by IR and H-1 NMR spectroscopy.