有机化学 ›› 2025, Vol. 45 ›› Issue (7): 2625-2629.DOI: 10.6023/cjoc202409009 上一篇    下一篇

研究简报

一种毛兰素的高效合成方法

王烁圻, 王成明*()   

  1. 暨南大学化学与材料学院 广州 511443
  • 收稿日期:2024-10-24 修回日期:2024-11-14 发布日期:2024-12-26
  • 基金资助:
    中央高校基本科研业务费(21620318); 中央高校基本科研业务费(2019QNGG22)

An Efficient Synthetic Route to Erianin

Shuoqi Wang, Chengming Wang*()   

  1. College of Chemistry and Materials Science, Jinan University, Guangzhou 511443
  • Received:2024-10-24 Revised:2024-11-14 Published:2024-12-26
  • Contact: *E-mail: cmwang2019@jnu.edu.cn
  • Supported by:
    Central University Basic Research Fund of China(21620318); Central University Basic Research Fund of China(2019QNGG22)

毛兰素是一种从石斛中提取出的低分子量天然化合物. 大量体外细胞毒性实验表明, 毛兰素具有显著的抗肿瘤活性, 其高效合成受到众多化学家和药物学家的关注. 以往报道的毛兰素合成步骤冗长、反应条件苛刻、难以在生产中应用. 此研究发展了一种新颖的毛兰素合成方法: 通过经典的Sonagashira偶联来构建二苯乙炔核心骨架, 经催化加氢, 最终以4步反应49%的总收率得到目标分子, 新路线具有反应条件温和、合成步骤简洁、实验操作简单和反应收率高等优点.

关键词: 毛兰素, 合成路线, Sonogashira偶联, 生物活性

Erianin, a low-molecular-weight natural product isolated from dendrobium, has demonstrated significant anti- tumor activity in numerous in vitro cytotoxicity experiments. As a result, its efficient synthesis has garnered considerable attention from chemists and pharmacologists. However, previously reported synthetic routes for Erianin are cumbersome and require harsh reaction conditions, rendering them unsuitable for large-scale industrial applications. This article mainly introduces a novel synthetic method for Erianin with a total yield of 49% (4 steps), featuring the construction of the core diphenyl acetylene motif via the classic Sonogashira coupling reaction, followed by catalytic hydrogenation. The new procedure enjoys mild reaction conditions, short synthetic steps, operational simplicity, and high efficiency.

Key words: Erianin, synthetic route, Sonogashira coupling, bioactive