Developing a straightforward route toward the synthesis of arylaminomaleimides by palladium-catalyzed arylation of one-pot synthesized aminomaleimides

3-Aryl-4-aminomaleimides have well-demonstrated applications, such as being used as fluorophores and inhibitors. However, their previous synthesis methods have involved tedious multi-step procedures or methods that need pre-functionalized maleimides and toxic or unstable reagents. Here, a feasible method is developed to synthesize these useful compounds. This includes the one-pot preparation of 3-aminomaleimides, followed by their direct arylation through a palladium-catalyzed Heck reaction with various aryl iodides regioselectively at the beta-position of their amine substituents. The results show that this method efficiently exhibits a broad scope. 3-Aryl-4-aminomaleimides are synthesized by one-pot preparation of 3-aminomaleimides, followed by their direct arylation regioselectively at the beta-position through a palladium-catalyzed Heck reaction with various iodoarenes.