Abstract
In this study, we present a highly efficient and environmentally benign protocol for synthesizing biologically important quinoxaline derivatives. The synthesis involves the reaction of 1,2-diamines with substituted phenacyl bromides or benzil, taking place at room temperature in N,N-dimethylformamide (DMF) solvent. The reaction is facilitated by a bifunctional heterogeneous catalyst composed of Al2O3–ZrO2 binary metal oxide. Our method offers numerous advantages, including excellent product yield, renewable catalytic conditions, minimal catalyst usage, safer chemistry, short reaction time, and a simple work-up procedure. To determine the chemical structure of the synthesized derivatives, we employed characterization techniques such as nuclear magnetic resonance (NMR) and high-resolution mass spectrometry (HRMS). Additionally, the Al2O3–ZrO2 catalyst was characterized using X-ray diffraction (XRD), scanning electron microscopy with energy-dispersive X-ray analysis (SEM-EDAX), and thermogravimetric analysis (TGA).
Graphical Abstract
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Acknowledgements
We are very much thankful to Chhatrapati Shahu Maharaj Research, Training and Human Development Institute (SARTHI), Pune for Junior Research Fellowship.
Disclosure statement
No potential conflict of interest was reported by the author(s).