Microwave-Assisted Synthesis of Pyrazinamide Derivatives: The Coupling Reaction of 3-Chloropyrazine-2-Carboxamide and Ring-Substituted Anilines

Title:Microwave-Assisted Synthesis of Pyrazinamide Derivatives: The Coupling Reaction of 3-Chloropyrazine-2-Carboxamide and Ring-Substituted Anilines

Volume: 12 Issue: 2

Author(s): Ondrej Jandourek, Martin Dolezal and Jiri Kunes

Affiliation:

Keywords: Aminodehalogenation, aniline, carboxamide, heterocycles, microwave synthesis, pyrazinamide, tuberculosis.

Abstract: A new approach for aminodehalogenation reaction between 3-chloropyrazine-2-carboxamide and ringsubstituted anilines is described. A series of 16 compounds (15 of them novel) derived from pyrazinamide have been synthesized successfully using the advantage of microwave-assisted reaction. The conditions for this aminodehalogenation reaction have been put to investigation to optimize the conversion, yield and time. The final methodology reduces the time needed for reaction from 24 hours using conventional heating to 30 minutes under microwave irradiation and increases the yield. The synthetic procedure together with analytical data of all compounds is presented. Lipophilicity properties were calculated and experimentally determined.

Cite this article as:

Jandourek Ondrej, Dolezal Martin and Kunes Jiri, Microwave-Assisted Synthesis of Pyrazinamide Derivatives: The Coupling Reaction of 3-Chloropyrazine-2-Carboxamide and Ring-Substituted Anilines, Current Organic Synthesis 2015; 12 (2) . https://dx.doi.org/10.2174/1570179411999141106101501