首页> 外文期刊>Russian Journal of Organic Chemistry >N-Hetaryl-2-cyanoacetamides in the Synthesis of Substituted (E)-N-Hetaryl-2-cyanoacrylamides, (E)-N-Alkyl-N-hetaryl-2-cyanoacrylamides, and 6-Amino-2-oxo-4-phenyl-1-(pyridin-2-yl)-1,2-dihydropyridine-3,5-dicarbonitriles
【24h】

N-Hetaryl-2-cyanoacetamides in the Synthesis of Substituted (E)-N-Hetaryl-2-cyanoacrylamides, (E)-N-Alkyl-N-hetaryl-2-cyanoacrylamides, and 6-Amino-2-oxo-4-phenyl-1-(pyridin-2-yl)-1,2-dihydropyridine-3,5-dicarbonitriles

机译:合成(E)-N-杂芳基-2-氰基丙烯酰胺,(E)-N-烷基-N-杂芳基-2-氰基丙烯酰胺和6-氨基-2-氧代-4的合成中的N-杂芳基-2-氰基乙酰胺-苯基-1-(吡啶-2-基)-1,2-二氢吡啶-3,5-二腈

获取原文
获取原文并翻译 | 示例
       

摘要

Knoevenagel condensation of N-hetaryl-substituted cyanoacetamides with aldehydes gave the cor-responding (E)-N-hetaryl-2-cyanoacrylamides which were converted into (E)-N-alkyl-N-hetaryl-2-cyanoacryl-amides and 6-amino-2-oxo-4-phenyl-1-(pyridin-2-yl)-1,2-dihydropyridine-3,5-dicarbonitriles. The structure of (E)-N-(pyridin-2-yl)-2-cyano-3-phenylprop-2-enamide was determined by X-ray analysis.
机译:N-杂芳基取代的氰基乙酰胺与醛的Knoevenagel缩合反应生成相应的(E)-N-杂芳基-2-氰基丙烯酰胺,将其转化为(E)-N-烷基-N-杂芳基-2-氰基丙烯酰胺和6 -氨基-2-氧代-4-苯基-1-(吡啶-2-基)-1,2-二氢吡啶-3,5-二碳腈。通过X射线分析来确定(E)-N-(吡啶-2-基)-2-氰基-3-苯基丙-2-烯酰胺的结构。

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