Skip to content
2000
Volume 18, Issue 1
  • ISSN: 1573-4137
  • E-ISSN: 1875-6786

Abstract

Background: Thiazolidinone-4-ones belong to important heterocyclic compounds because of their broad spectrum of biological activities. Several methods for the synthesis of 4- thiazolidinones are reported in the literature. The main synthetic route to synthesize 1,3-thiazolidin- 4-ones is the three-component reaction between amine, a carbonyl compound and a mercapto-acid. Objective: Dapsone-Cu supported on silica coated FeO (FeO@SiO-pr@dapsone-Cu) as a new heterogeneous nanoparticle catalyst was synthesized and the structure and morphology of this catalyst were characterized by Fourier transform infrared spectroscopy (FT-IR), Xray diffraction (XRD), transmission electron microscopy (TEM), field emission scanning electron microscopy (FESEM), energy-dispersive X-ray spectroscopy (EDX), zeta potential, vibrating sample magnetometry (VSM) and thermal gravimetric analysis (TGA). The new synthesized catalyst was applied as an effective nanocatalyst for the synthesis of new derivatives of azo-linked thiazolidinones through one-pot multi-component reaction of various aromatic aldehydes, thioglycolic acid and 4- aminoazobenzene under solvent-free condition. Methods:A mixture of aldehyde, thioglycolic acid, 4-aminoazobenzene (1 mmol) and 0.05 g FeO@SiO@dapsone-Cu MNPs was stirred at room temperature under solvent-free condition. Results: A facile, green, new and efficient method for the synthesis of thiazolidine-4-ones through three component reaction of various aldehydes, thioglycolic acid and 4-aminoazobenzene in the presence of FeO@SiO-propyl@dapsone-Cu complex under solvent-free reaction was reported. Conclusion: This new procedure has notable advantages such as excellent yields, short reaction time, operational simplicity, easy work-up, eco-friendly and using a non-toxic catalyst. Also, the catalyst is easily recoverable in the presence of an enormous magnet and reused for six consecutive reaction cycles without significant loss of activity.

Loading

Article metrics loading...

/content/journals/cnano/10.2174/1573413717666210226120252
2022-01-01
2025-09-28
Loading full text...

Full text loading...

/content/journals/cnano/10.2174/1573413717666210226120252
Loading
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test