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A series of Michael adducts (5-11) have been synthesized with good yields under solvent-free microwave conditions. Aliphatic and aromatic amines utilized as Michael donors reacted with 1(4,7-dimethoxybenzo[b]thiophen-2-yl)-2-propen-1-one (4), to produce β-aminoketones and azaheterocyclic compounds of potential biological interest.

Solvent-free microwave-promoted Michael addition of aza-nucleophiles to benzo[b]thiophen-2-yl-2-propenone