LAUSR.org creates dashboard-style pages of related content for over 1.5 million academic articles. Sign Up to like articles & get recommendations!

Gluconic acid promoted cascade reactions of 2-phenylimidazo[1,2-a] pyridine-3-carbaldehyde with cyclohexane-1,3-dione to create novel fused bisheterocycles

Photo by andreacaramello from unsplash

Abstract Here in, we described the synthesis of novel bisheterocycles imidazopyridine bearing xanthenedione by reacting various substituted 2-phenylimidazo [1,2-a] pyridine-3-carbaldehyde with cyclohexane-1,3-dione in gluconic acid aqueous solution (GAAS) via a… Click to show full abstract

Abstract Here in, we described the synthesis of novel bisheterocycles imidazopyridine bearing xanthenedione by reacting various substituted 2-phenylimidazo [1,2-a] pyridine-3-carbaldehyde with cyclohexane-1,3-dione in gluconic acid aqueous solution (GAAS) via a tandem Knoevenagel followed by Michael, cyclization & tautomerization sequence. The use of GAAS in organic synthesis offers significant benefits like cost-effective, simple operation, reusable catalyst and green method. The reaction completed in 2–12 h to afford white stable solid compounds with very good yield. The structures of the compounds are confirmed by analyzing MS, IR, 1H NMR and 13C NMR spectra. Further, the structure of compound 3 h was confirmed by XRD analysis. GRAPHICAL ABSTRACT

Keywords: novel; pyridine carbaldehyde; phenylimidazo pyridine; gluconic acid; carbaldehyde cyclohexane; cyclohexane dione

Journal Title: Synthetic Communications
Year Published: 2019

Link to full text (if available)


Share on Social Media:                               Sign Up to like & get
recommendations!

Related content

More Information              News              Social Media              Video              Recommended



                Click one of the above tabs to view related content.