Tetrabutylammonium bromide-Cesium carbonate: new reagent system for the synthesis of substituted pyridines at room temperature
Authors
Abstract:
The highly substituted pyridine derivatives are found to exhibit diverse pharmacological activities. They are also emerged as potential medicinal leads in developing therapeutic agents for the treatment of various diseases. In this work, a series of 2-amino-3,5-dicarbonitrile-6-thio-pyridine derivatives have been synthesized at room temperature via one-pot, multi-component reaction of various aromatic aldehydes, malononitrile and thiophenols using catalytic amount of tetrabutylammonium bromide (TBAB) and cesium carbonate in methanol. In the present method, the use of thermal condition is avoided. In addition, the advantages such as operational simplicity, economic viability, ecologically benign nature make this protocol a very efficient alternative to the literature methods.
similar resources
tetrabutylammonium bromide-cesium carbonate: new reagent system for the synthesis of substituted pyridines at room temperature
the highly substituted pyridine derivatives are found to exhibit diverse pharmacological activities. they are also emerged as potential medicinal leads in developing therapeutic agents for the treatment of various diseases. in this work, a series of 2-amino-3,5-dicarbonitrile-6-thio-pyridine derivatives have been synthesized at room temperature via one-pot, multi-component reaction of various a...
full textBi(NO3)3.5H2O: An efficient acidic reagent for synthesis of azo dyes at room temperature
An one-pot method has been developed for the synthesis of azo dyes via sequential diazotization–diazo coupling of aromatic amines with coupling agents at room temperature in the presence of Bi(NO3)3. 5H2O. Short reaction times, high yields, a clean process, simple methodology, easy work-up and green conditions are advantages of this protocol.
full textBi(NO3)3.5H2O: An efficient acidic reagent for synthesis of azo dyes at room temperature
An one-pot method has been developed for the synthesis of azo dyes via sequential diazotization–diazo coupling of aromatic amines with coupling agents at room temperature in the presence of Bi(NO3)3. 5H2O. Short reaction times, high yields, a clean process, simple methodology, easy work-up and green conditions are advantages of this protocol.
full textKaolin-SO3H nanoparticles: A new efficient and reusable catalyst for synthesis of 2-substituted benzimidazoles at room temperature
Kaolinite clay found its application in medicine, in toothpaste, in cosmetic and as a food additive. Recently, a specially formulated spray is used in fruit and vegetable production to repel the insects and prevent sunburn. Kaolin-SO3H nanoparticles were prepared via reaction of kaolin and chlorosulfonic acid and characterized by FT-IR, XRD, FESEM, TEM, XRF, EDS, BET and TGA. 2-Substituted benz...
full textTetrabutylammonium Bromide System
Vapor-liquid equilibrium and density measurements have been performed on 1.00-5.89 m tetrabutylammonium bromide (TBAB) in mixtures of 2-propanoland water. The VLE experiments were performed using a modified Othmer still a t ambient pressure. The effect of salt on the relative volatility of 2-propanol was evaluated at molalities of 1.00,1.79, and 5.89 over the full range of solvent composition. ...
full textbi(no3)3.5h2o: an efficient acidic reagent for synthesis of azo dyes at room temperature
an one-pot method has been developed for the synthesis of azo dyes via sequential diazotization–diazo coupling of aromatic amines with coupling agents at room temperature in the presence of bi(no3)3. 5h2o. short reaction times, high yields, a clean process, simple methodology, easy work-up and green conditions are advantages of this protocol.
full textMy Resources
Journal title
volume 4 issue Issue 2, pp. 133-235
pages 186- 197
publication date 2016-04-01
By following a journal you will be notified via email when a new issue of this journal is published.
Hosted on Doprax cloud platform doprax.com
copyright © 2015-2023