Issue 123, 2015

Facile synthesis of pyranopyrazoles and 3,4-dihydropyrimidin-2(1H)-ones by a Ti-grafted polyamidoamine dendritic silica hybrid catalyst via a dual activation route

Abstract

A simple, highly efficient and ecofriendly approach for the preparation of biologically potent pyranopyrazoles and 3,4-dihydropyrimidin-2(1H)-ones are described here. A Ti-grafted polyamidoamine dendritic silica hybrid catalyst was successfully synthesized, and its catalytic performance was studied in two important multicomponent reactions such as Biginelli reaction and pyranopyrazole synthesis. Studies demonstrate that the crystalline pore wall structure of the dendritic silica hybrid catalyst makes adsorption of reactants easy. Combining the Lewis acidic and Lewis basic properties of the silica surface facilitates and accelerates the synthesis of the desired products in high yields. The key advantages of the present method are the excellent yield of the products, low catalyst loading, shorter reaction times, facile work-up, and purification of the products by non-chromatographic methods and the reusability of the catalyst.

Graphical abstract: Facile synthesis of pyranopyrazoles and 3,4-dihydropyrimidin-2(1H)-ones by a Ti-grafted polyamidoamine dendritic silica hybrid catalyst via a dual activation route

Supplementary files

Article information

Article type
Paper
Submitted
19 Aug 2015
Accepted
13 Nov 2015
First published
16 Nov 2015

RSC Adv., 2015,5, 101776-101788

Facile synthesis of pyranopyrazoles and 3,4-dihydropyrimidin-2(1H)-ones by a Ti-grafted polyamidoamine dendritic silica hybrid catalyst via a dual activation route

P. S. Sinija and K. Sreekumar, RSC Adv., 2015, 5, 101776 DOI: 10.1039/C5RA16723J

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