ABSTRACT The synthesis of a series of functionalized 1-Benzyl-3-[4-Aryl-1-piperazingl] carbonyl-1H-Indoles 6 (af), as a potential new class of bioactive ligands at D 4 receptors is reported. The synthetic strategy took place through a five steps sequence to provide indole amides 6 (af) in 75-92% yield.