Reactions of an imidazo[4,5-c]isoxazole-6-carboxylate with dimethyl acetylenedicarboxylate; formation of the first example of a [1,4]diazepino[2,3-c]isoxazole
A. Taher et al., Reactions of an imidazo[4,5-c]isoxazole-6-carboxylate with dimethyl acetylenedicarboxylate; formation of the first example of a [1,4]diazepino[2,3-c]isoxazole, TETRAHEDR L, 41(48), 2000, pp. 9319-9321
The synthesis of the first example of a [1,4]diazepino[2,3-c]isoxazole deri
vative is reported. Reaction of an imidazo[4,5-c]isoxazole with acetylenic
esters has been shown to lead to the formation of 2-pyrrol-2-yl imidazoles,
Here we report an alter-native reaction pathway in which the fused imidazo
le ring adds a molecule of acetylenic eater, and undergoes ring expansion t
o a fused El, il]diazepine. A mechanism for the reaction is discussed. (C)
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