摘要

A novel and efficient preparation of pyrazolo[3,4-b]pyridine (5) and pyrazolo[3,4-b]pyridin-6-one (8) derivatives from the condensation of arylidenecyanothioacetamide (1) or arylidenecyanoacetamide (7) with 5-amino3-methyl-1-phenylpyrazole (4) in [bmim]BF4 is reported for the first time. The mechanism for the formation of 5 from I and 4, or 8 from 7 and 4, and the comparison between the reactivity of thioamide group versus amide group are briefly discussed.

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