有机化学 ›› 2025, Vol. 45 ›› Issue (9): 3361-3369.DOI: 10.6023/cjoc202503008 上一篇    下一篇

研究论文

氧化铝促进的咪唑并[1,2-a]吡啶与α,β-不饱和酮的Michael加成

孙亚栋a,c,*(), 周海a, 郑土才a, 王守才b, 及方华b,*()   

  1. a 衢州学院化学与材料工程学院 衢州 324000
    b 桂林理工大学化学与生物工程学院 桂林 541004
    c 新疆大学化学与化工学院 乌鲁木齐 830046
  • 收稿日期:2025-03-07 修回日期:2025-05-06 发布日期:2025-06-06
  • 基金资助:
    国家自然科学基金(21662032); 国家自然科学基金(22061013); 衢州学院科研启动基金(BSYJ202108)

Alumina-Promoted Michael Addition of Imidazo[1,2-a]pyridines with α,β-Unsaturated Ketones

Yadong Suna,c,*(), Hai Zhoua, Tucai Zhenga, Shoucai Wangb, Fanghua Jib,*()   

  1. a College of Chemical and Material Engineering, Quzhou University, Quzhou 324000
    b College of Chemistry and Bioengineering, Guilin University of Technology, Guilin 541004
    c College of Chemistry and Chemical Engineering, Xinjiang University, Urumqi 830046
  • Received:2025-03-07 Revised:2025-05-06 Published:2025-06-06
  • Contact: E-mail: syd19791016@163.com; fanghuaji@glut.edu.cn
  • Supported by:
    National Natural Science Foundation of China(21662032); National Natural Science Foundation of China(22061013); Startup Funds of Quzhou University(BSYJ202108)

开发了一种以酸性氧化铝为路易斯酸, 咪唑并[1,2-a]吡啶与α, β-不饱和酮的直接Michael加成反应. 酸性氧化铝表面丰富的路易斯酸位点(Al3⁺)能够高效活化α,β-不饱和酮的羰基, 显著提高β-碳的亲电性, 从而促进咪唑并[1,2-a]吡啶C3位的选择性烷基化. 该方法具有优异的官能团兼容性、温和的反应条件、低廉的试剂成本和操作方便等特点, 为烷基化的咪唑并[1,2-a]吡啶的高效合成提供了新策略.

关键词: 路易斯酸, 咪唑并[1,2-a]吡啶, α,β-不饱和酮, Michael加成

A direct Michael addition reaction between imidazo[1,2-a]pyridines and α,β-unsaturated ketones using acidic alumina as a C(sp3)—H acid catalyst has been developed. The abundant C(sp3)—H acid sites (Al3⁺) on the acidic alumina surface effectively activate the carbonyl group of α,β-unsaturated ketones, significantly enhancing the electrophilicity of the β-carbon and thereby facilitating selective alkylation at the C3 position of imidazo[1,2-a]pyridines. This method demonstrates excellent functional group compatibility, mild reaction conditions, low reagent costs, and operational simplicity, providing a novel strategy for the efficient synthesis of alkylated imidazo[1,2-a]pyridine derivatives.

Key words: C(sp3)—H acid, imidazo[1,2-a]pyridine, α,β-unsaturated ketone, Michael addition