期刊文献+

咪唑并吡啶类化合物的合成及其应用 被引量:9

Advances in Synthesis and Application of Imidazopyridine Derivatives
原文传递
导出
摘要 咪唑并吡啶类化合物具有与吲哚、氮杂吲哚等类似的特殊结构和良好的生物活性,在医药和农药工业有着广泛的应用,成为有机化学家和药物化学家的研究热点。咪唑并吡啶类化合物主要有咪唑并[4,5-b]吡啶、咪唑并[4,5-c]吡啶、咪唑并[1,2-a]吡啶和咪唑并[1,5-a]吡啶等4个类型。本文阐述了近年来咪唑并吡啶类化合物的合成研究进展和应用情况,主要介绍了咪唑并[4,5-b]吡啶和咪唑并[4,5-c]吡啶这两类化合物的合成方法和在医药及农药领域的应用。 Imidazopyridine derivatives are of great importance for their remarkable biological properties.Their structrues are similar to those of indoles and azaindoles,two important heterocycles involved in many alkaloids.Many of them have been demonstrated as inhibitors of the target enzymes and used as medicines,herbicides and fungicides.The imidazopyridines comprise four important isomers:imidazo[4,5-b]pyridine,imidazo[4,5-c] pyridine,imidazo[1,2-a]pyridine,imidazo[1,5-a]pyridine.This paper reviews the advances in synthesis and application on imidazopyridines such as imidazo[4,5-b]pyridine and imidazo[4,5-c]pyridine derivatives in recent years.
出处 《化学进展》 SCIE CAS CSCD 北大核心 2010年第4期631-638,共8页 Progress in Chemistry
基金 中国博士后科学基金项目(No.20080431024) 中南大学博士后科学基金 湖南省科技计划博士后专项(No.2009RS3029)资助
关键词 咪唑并吡啶 杂环化合物 合成 imidazopyridine derivatives heterocycles synthesis
  • 相关文献

参考文献1

二级参考文献14

  • 1Wang, J.; Mason, R.; VanDerveer, D.; Feng, K.; Bu, X. R. J. Org. Chem. 2003, 68(13), 5415.
  • 2Wang, J.; Dyers, L.; Mason, R.; Amoyaw, P.; Bu, X. R. J. Org. Chem. 2005, 70(6), 2353.
  • 3Kappe, C. O. Angew. Chem., Int. Ed. 2004, 43(46), 6250.
  • 4Bourdais, J.; Omar, A.-M. E. J. Heterocycl. Chem. 1980, 17(3), 555.
  • 5Benincori, T.; Brenna, E.; Sannicolo, F. J. Chem. Soc., Perkin Trans. 1 1993, 675.
  • 6Browne, L. J.; Gude, C.; Rodriguez, H. J. Med. Chem. 1991, 34(2), 725.
  • 7Durant, G. J.; Loynes, J. M.; Wright, S. H. B. J. Med. Chem. 1973, 16(11), 1272.
  • 8Ford, N. F.; Browne, L. J.; Campell, T.; Gemenden, C.; Goldstein, R.; Gude, C.; Waley, J. W. F. J. Med. Chem. 1985, 28(2), 164.
  • 9Gueiffier, A.; Lhassani, M.; Elhakmaoui, A.; Snoeck, R.; Andrei, G.; Chavignon, O.; Teulade, J.-C.; Kerbal, A.; Essassi, E. M.; Debouzy, J.-C.; Witvrouw, M.; Blache, Y.; Balzarini, J.; Clercq, E. D.; Chapet, J.-P. J. Med. Chem. 1996, 39(14), 2856.
  • 10Kaminki, J. J.; Bristol, J. A.; Lovey, R. G.; Elliot, A. J.;Duzik, H.; Solomon, D. M.; Conn, D. J.; Domalski, M. S.; Wong, S.-C.; Gold, E. H.; Long, J. F.; Chiu, P. J. S.; Steinberg, M.; McPhail, A. T. J. Med. Chem. 1985, 28(7), 876.

共引文献3

同被引文献69

  • 1江镇海.吡啶类化合物在农药中的发展动态[J].农药市场信息,2009(17):28-28. 被引量:2
  • 2李英奇,彭雨春.合成芳基硼酸及其酯的研究进展[J].化学试剂,2006,28(3):149-152. 被引量:13
  • 3邓毅,赵爱华,尹龙萍,邱明丰,贾伟.黄芩苷-铬(Ⅲ)配合物的合成与表征[J].中国天然药物,2007,5(1):38-41. 被引量:22
  • 4任青云,贺红武,刘建超.四氢苯并[4',5']噻吩并[3',2':5,6]吡啶并[4,3-d]嘧啶-4(3H)-酮的合成、晶体结构及杀菌活性[J].有机化学,2007,27(3):397-401. 被引量:13
  • 5John E S,Thomas A M,Alfred R C,et al.Synthesis and biological activity of 3-substituted imidazo[1,2-a]pyridines as antiulcer agents[J].Journal of Medicinal Chemistry,1989,32(9):2204-2210.
  • 6Patricia C Lima,Mitchell A Avery,Babu L Tekwani,et al.Synthesis and biological evaluation of new imidazo[1,2-a]pyridine derivatives designed as mefloquineanalogues[J].Farmaco,2002,57(10):825-832.
  • 7Zaesung No,Jaeseung Kim,Priscille Brodin Brodin,et al.Preparation of imidazopyridine derivatives as anti-infective compounds[P].WO2011113606,2011.
  • 8Garrett C M,Lowell D M,Philip A H,et al.Advent of imidazo[1,2-a]pyridine-3-carboxamides with potent multi-and extended drug resistant antituberculosis activity[J].ACS Medicinal Chemistry Letters,2011,2(6):466-470.
  • 9Gudmundsson Kristjan,Turner Elizabeth Madalena.Imidazo[1,2-a]pyridine-3-carboxamides as anti-HIV agents and their preparation,pharmaceutical compositions and their use in monotherapy and in combination therapy of diseases[P].WO2007087548,2007.
  • 10Orazio A.Attanasi,Luca Bianchi,Linda A.Campisi,et al.A novel solvent-free approach to imidazole containing nitrogen-bridgehead heterocycles[J].Organic Letters,2013,15(14):3646-3649.

引证文献9

二级引证文献7

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部