پديدآورندگان :
Zolfigol Mohammad Ali mzolfigol@yahoo.com Bu-Ali-Sina University , Zarei Mahmoud Bu-Ali-Sina University , Moosavi-Zare Ahmad Reza Sayyed Jamaleddin Asadabadi University, Asadabad , Noroozizadeh Ehsan Bu-Ali-Sina University
چكيده فارسي :
Quinoline derivatives with a 1,4-dihydropyridine scaffold are promising structures because
of their pharmacological properties.Hexahydroquinolines (HHQs) have used as anti-bacterial,
anti-hypertensive, antimalarial, anti-inflammatory, antiasthamatic, and tyrosine kinase
inhibiting agents [1,2]. Some methods and catalysts have been reported for the preparation of
HHQs [3,4]. In this work, we have used di-Sulfonic acid imidazolium
chloroaluminate[Dsim]AlCl4as an efficient, heterogeneous, and reusable catalyst for the
synthesis of hexahydroquinolines by the One-Pot multi-component condensation reaction of
dimedone aryl aldehydes, (5,5-dimethylcyclohexane-1,3-dione), β-ketoesters and ammonium
acetate under solvent-free conditions (Figure).