首页> 外文期刊>Chemical and Pharmaceutical Bulletin >An efficient green multi-component reaction strategy for the synthesis of highly functionalised pyridines and evaluation of their antibacterial activities
【24h】

An efficient green multi-component reaction strategy for the synthesis of highly functionalised pyridines and evaluation of their antibacterial activities

机译:一种高效的绿色多组分反应策略,用于合成高度官能化的吡啶并评估其抗菌活性

获取原文
获取原文并翻译 | 示例
           

摘要

An efficient green multi-component reaction (MCR) method has been developed for the synthesis of 2-amino-4-aryl/heteroaryl-6-(pyridin-2-ylthio)pyridine-3, 5-dicarbonitrile(s) via a 3-component reaction of aryl aldehyde(s), malononitrile and 2-mercaptopyridine in the presence of K_2CO _3 under solvent free reaction conditions (SFRC) using grinding technique at room temperature in a single step. The advantages of the present protocol is operationally simple, environmentally benign, solvent-free reaction conditions (SFRC), simple work up, excellent isolated yields of desired products and viable method for large scale applications in pharmaceutical industry. Interestingly, the synthesized compounds showed moderate to excellent antibacterial activities against Gram-positive and Gram-negative bacterial strains.
机译:已开发出一种有效的绿色多组分反应(MCR)方法,可通过3来合成2-氨基-4-芳基/杂芳基-6-(吡啶-2-基硫基)吡啶-3,5-二碳腈在无溶剂反应条件(SFRC)下,在室温下,通过一步研磨技术,在无溶剂反应条件下(SFRC),芳基醛,丙二腈和2-巯基吡啶的芳烃反应。本方案的优点是操作简单,对环境无害,无溶剂反应条件(SFRC),后处理简单,所需产品的优良分离产率以及在制药工业中大规模应用的可行方法。有趣的是,合成的化合物显示出对革兰氏阳性和革兰氏阴性细菌菌株的中等至优异的抗菌活性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号