研究论文

一锅法合成多取代色酮并双环吡啶类化合物

  • 陈亮 ,
  • 王保取 ,
  • 赵宇澄 ,
  • 严胜骄 ,
  • 林军
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  • 云南大学化学科学与工程学院 教育部自然资源药物化学重点实验室 昆明 650091

收稿日期: 2016-12-12

  修回日期: 2017-01-21

  网络出版日期: 2017-02-20

基金资助

国家自然科学基金(Nos.U1202221,21362042,21262042,21662042)、云南省后备人才(No.2012HB001)、云南大学青年英才计划(No.XT412003)资助项目.

One-Pot Synthesis of Multisubstituted Chromone-Fused Bicyclic Pyridine Compounds

  • Chen Liang ,
  • Wang Baoqu ,
  • Zhao Yucheng ,
  • Yan Shengjiao ,
  • Lin Jun
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  • Key Laboratory of Medicinal Chemistry for Natural Resource, Ministry of Education, School of Chemical Science andTechnology, Yunnan University, Kunming 650091

Received date: 2016-12-12

  Revised date: 2017-01-21

  Online published: 2017-02-20

Supported by

Project supported by the National Natural Science Foundation of China (Nos. U1202221, 21362042, 21262042, 21662042), the Talent Found in Yunnan Province (No. 2012HB001), and the Excellent Young Talents of Yunnan University (No. XT412003).

摘要

建立了一种简捷、绿色合成多取代色酮并双环吡啶类化合物的合成方法.该方法是利用色酮-3-甲醛1N-苄基硝基烯酮缩胺(NBNKAs,2)在乙醇中反应,一步合成色酮并双环吡啶化合物.通过直接抽滤得目标产物3,无需额外的后处理操作.该方法具有合成成本低,反应溶剂生物相容性好,反应条件温和,原子经济性,高产率(93~98%)及产物具有潜在的生物活性等显著优势.

本文引用格式

陈亮 , 王保取 , 赵宇澄 , 严胜骄 , 林军 . 一锅法合成多取代色酮并双环吡啶类化合物[J]. 有机化学, 2017 , 37(6) : 1433 -1442 . DOI: 10.6023/cjoc201612038

Abstract

A concise and environment friendly route for the synthesis of multisubstituted chromone-fused bicyclic pyridine compounds via one-step reaction of chromone-3-carboxaldehyde 1 and N-benzyl nitro ketene aminals (NBNKAs, 2) in ethanol media has been developed. The targeted compounds 3 can efficiently obtain by filter without extra post-treatment. The reaction is particularly attractive due to following features: low-cost and biocompatibility solvent, mild temperature, atom economy, high yields, and potential biological activity.

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