Issue 5, 2015

Nickel nanoparticles assisted regioselective synthesis of pyrazoloquinolinone and triazoloquinazolinone derivatives

Abstract

Biologically important pyrazoloquinolinone and triazoloquinazolinone derivatives were synthesized by the condensation reaction of 3-amino-1H-1,2,4-triazole/3-amino-5-methyl-1H-pyrazole, dimedone and aryl aldehydes using catalytic amount of magnetically retrievable nickel nanoparticles under reflux condition. This protocol eliminates the usage of toxic reagents, complex work-up conditions, etc., with the added benefit of reusability of the catalyst without compromising the yield or purity of the product.

Graphical abstract: Nickel nanoparticles assisted regioselective synthesis of pyrazoloquinolinone and triazoloquinazolinone derivatives

Supplementary files

Article information

Article type
Paper
Submitted
22 Dec 2014
Accepted
24 Feb 2015
First published
25 Feb 2015

New J. Chem., 2015,39, 3908-3915

Nickel nanoparticles assisted regioselective synthesis of pyrazoloquinolinone and triazoloquinazolinone derivatives

N. G. Singh, R. Nagarajaprakash, J. W. S. Rani, C. Kathing, R. Nongrum and R. Nongkhlaw, New J. Chem., 2015, 39, 3908 DOI: 10.1039/C4NJ02372B

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