Synthetic Communications p. 2561 - 2571 (2019)
Update date:2022-08-28
Topics:
Bakhta, Saléha
Kabri, Youssef
Crozet, Maxime D.
Nedjar-Kolli, Bellara
Vanelle, Patrice
A series of imidazo[1,2-a]pyridinylpropenenitriles were synthesized via consecutive one-pot Suzuki–Miyaura and Knoevenagel reactions in water/ethanol mixture between imidazo[1,2-a]pyridine-2-carbaldehydes, arylboronic acids and malononitrile, methyl cyanoacetate or ethyl cyanoacetate. This environmental friendly procedure tolerates a wide range of boronic acids and affords a new substituted imidazo[1,2-a]pyridinyl propenenitriles in good yields under microwave irradiation.
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