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

被引:2
|
作者
Jandourek, Ondrej [1 ]
Dolezal, Martin [1 ]
Kunes, Jiri [2 ]
机构
[1] Charles Univ Prague, Fac Pharm Hradec Kralove, Dept Med Chem & Pharmaceut Anal, Hradec Kralove 50005, Czech Republic
[2] Charles Univ Prague, Fac Pharm Hradec Kralove, Dept Organ & Inorgan Chem, Hradec Kralove 50005, Czech Republic
关键词
Aminodehalogenation; aniline; carboxamide; heterocycles; microwave synthesis; pyrazinamide; tuberculosis; ORGANIC-SYNTHESIS; MYCOBACTERIUM-TUBERCULOSIS; ARYL HALIDES; AMINATION; ACID; ANTIMYCOBACTERIAL; CHLORIDES;
D O I
10.2174/1570179411999141106101501
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A new approach for aminodehalogenation reaction between 3-chloropyrazine-2-carboxamide and ring-substituted 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.
引用
收藏
页码:189 / 196
页数:8
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