Arul Murugesan; Robert M Gengan; Kandasamy G Moodley; Gerhard Gericke
Abstract
Boron nitride nanomaterial based solid acid catalyst is an efficient and reusable sulfonic acid catalyst for the one-pot synthesis of 9-(2-(4-ethylpiperazin-1-yl)quinolin-3-yl)-3,3-dimethyl-3,4,9,10-tetrahydroacridin-1(2H)-one derivatives under microwave irradiation conditionsvia. The Knoevenagel and ...
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Boron nitride nanomaterial based solid acid catalyst is an efficient and reusable sulfonic acid catalyst for the one-pot synthesis of 9-(2-(4-ethylpiperazin-1-yl)quinolin-3-yl)-3,3-dimethyl-3,4,9,10-tetrahydroacridin-1(2H)-one derivatives under microwave irradiation conditionsvia. The Knoevenagel and Michael type reactions. The catalyst was prepared by simply mixing boron nitride and 3-amino-4-methoxybenzenesulfonic acid in a safe method. The morphological properties of the catalyst was determined by using FT-IR, XRD, TEM, SEM and Raman spectroscopy. The synthesised catalyst was employed in a Knoevenagel and Michael type reaction to synthesise novel ethylpiperazinyl-quinolinyl based acridine derivatives. Furthermore, the newly-synthesised compounds was used for molecular docking in Hsp90 protein studies. The method developed in this study has the advantages of good yield, simplicity coupled with safety and short reaction time. Most importantly it was found that the solid acid catalyst can be recycled with minimal loss of activity over five cycles.
T. Muthu; K. Anand; M. Sureshkumar; R. M. Gengan
Abstract
An efficient one-pot multi-component synthesis of medicinally important 2-amino-4H-pyran-3-carbonitrile derivatives using a new heterogeneous calcium loaded boron nitride (CaBNT) catalyst is described herein. This transformation transpires by Knoevenagel condensation, Michael addition and intramolecular ...
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An efficient one-pot multi-component synthesis of medicinally important 2-amino-4H-pyran-3-carbonitrile derivatives using a new heterogeneous calcium loaded boron nitride (CaBNT) catalyst is described herein. This transformation transpires by Knoevenagel condensation, Michael addition and intramolecular cyclization. Alkaline earth metal-based green catalyst was successfully prepared and characterized by XRD, SEM with EDX, Raman spectroscopy, BET, DSC-TGA and FT-IR. The reaction works up is facile and CaBNT catalyst can easily be separated from the reaction mixture and re-used more than five times in subsequent reactions. This methodology offers several advantages such as excellent yields, use of inexpensive solvent and relatively shorter reaction time.
