Multicomponent reaction achieves 73-94% yields in the synthesis of pyrano-pyrazolo-pyridones, suggesting benefits of the bimetallic catalyst and magnetic separation.
A novel series of pyranopyrazolopyridone derivatives was synthesized via multicomponent reaction involving 4-hydroxy-6-methylpyridin-2-ones, aromatic aldehydes, and pyrazolone. To this end, a new high-efficiency bimetallic cobalt-cadmium heterogeneous magnetic catalyst was designed, synthesized, characterized, and used in this reaction. Instrumental techniques such as elemental analysis (CHN), EDX, SEM, TEM, FT-IR, XRD, VSM, and TGA were used to characterize the catalyst. To maximize efficiency, reaction conditions were optimized across all parameters, including temperature, time, and the amount of catalyst used. In the optimized reaction conditions, 78 °C and 10 h in the presence of 25 mol% of the catalyst, 73-94% isolated yields of pyranopyrazolopyridone derivatives were obtained in an ethanolic solution. Key advantages of this synthesis include operational simplicity, relatively short reaction time, use of an environmentally friendly heterogeneous bimetallic catalyst, and easy magnetic separation.
No takes yet. Share an insight, caveat, or question.
Kamali et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: