3,4-dihydropyrimidinones and their derivatives are synthesized via biginelli routes involving an aromatic aldehydes, ethylacetoacetates and urea in one-pot procedure by using cds nanoparticles as efficient heterogeneous catalyst in solvent-free conditions. compared with classical biginelli reaction reported in 1893, this new method provides much improved modification in terms of simplicity. the...

The Biginelli reaction was combined with the Passerini reaction for the first time in a sequential multicomponent tandem reaction approach. After evaluation of all possible linker components and a suitable solvent system, highly functionalized dihydropyrimidone-α-acyloxycarboxamide compounds were obtained in good to excellent yields. In a first reaction step, different 3,4-dihydropyrimidin-2(1H...

Hmim][Tfa] was tested as catalyst for the Biginelli reaction multicomponent reaction under conventional and non conventional heat source i.e. Microwave heating. Low catalyst loading, reduced reaction time and operational simplicity are the main highlights of this proposed protocol. Using our proposed protocol, we tested 30 different biologically active compounds in good yield.

3,4-Dihydropyrimidin-2(1H)-ones were synthesised in high yields by one-pot three-component Biginelli condensation in the presence of room temperature ionic liquids such as 1-n-butyl-3-methylimidazolium tetrafluoroborate (BMImBF4) or hexafluorophosphorate (BMImPF6) as catalysts under solvent-free and neutral conditions. © 2001 Elsevier Science Ltd. All rights reserved. Recently, the interest in ...

Introduction and Aim: An efficient aspect of two step synthesis tetrahydro pyrimidine carboxamide derivatives were developed by Biginelli reaction. The two-step synthesized 1,2,3,4-tetrahydropyrimidinecarboxamide compounds evaluated In-vitro studies like antifungal bacterial activities. Few shown excellent zone inhibition against fungal Microbial In this study showed significant effect action d...