研究简报

微波辐射下一步合成4-芳基-2,6-二(3,3'-香豆素基)吡啶衍生物

  • 周建峰 ,
  • 娄风文 ,
  • 孙小军 ,
  • 安礼涛 ,
  • 支三军 ,
  • 霍娟娟 ,
  • 郑丽 ,
  • 王星帅
展开
  • 淮阴师范学院化学化工学院, 江苏省低维材料化学重点建设实验室, 淮安 223300

收稿日期: 2012-02-05

  修回日期: 2012-03-22

  网络出版日期: 2012-04-10

基金资助

江苏省低维材料化学重点建设实验室开放基金(JSKC11101)资助项目.

One-Pot Synthesis of 3,3'-(4-arylpyridine-2,6-diyl)-bis (2H-chromen-2-one) Derviatives under Microwave Irradiation

  • Zhou ,
  • Jianfeng Lou ,
  • Fengwen Sun ,
  • Xiaojun An ,
  • Litao Zhi ,
  • Sanjun Huo ,
  • Juanjuan Zheng ,
  • Li Wang
Expand
  • School of Chemistry and Chemical Engineering, Jiangsu Key Laboratory for Chemistry of Low-Dimensional Materials, Huaiyin Normal University, Huai’an 223300

Received date: 2012-02-05

  Revised date: 2012-03-22

  Online published: 2012-04-10

Supported by

Project supported by Jiangsu Key Laboratory for Chemistry of Low-Dimensional Materials (JSKC11101 ).

摘要

3-乙酰基香豆素、芳醛和醋酸铵在醋酸溶剂中经微波辐射, 一步合成了4-芳基-2,6-二(3,3'-香豆素基)吡啶衍生物,反应在5~8 分钟内完成,产率60~86%,具有反应时间短、操作简便和环境友好等优点.所以产物经红外光谱、氢谱、质谱和元素分析表征.

本文引用格式

周建峰 , 娄风文 , 孙小军 , 安礼涛 , 支三军 , 霍娟娟 , 郑丽 , 王星帅 . 微波辐射下一步合成4-芳基-2,6-二(3,3'-香豆素基)吡啶衍生物[J]. 有机化学, 2012 , 32(06) : 1112 -1115 . DOI: 10.6023/cjoc1202054

Abstract

A series of 3,3'-(4-arylpyridine-2,6-diyl)bis(2H-chromen-2-one) derviatives were synthesized by the one-pot three-component reaction of 3-acetyl coumarin, aromatic aldehydes, and ammonium acetate in acetic acid under microwave irradiation. The reactions were completed in 5~8 min with 60%~86% yields, and the procedure has the advantages of short reaction time, easy work-up and environmental begin. Their structures were confirmed by 1H NMR, IR, MS techniques and elemental analysis.

参考文献

[1] Ferrer J. M.; Leiton M. J. Zaton, A. M. L. J. Protein Chem. 1998, 17, 115.  
[2] Janis, R. A.; Siler, P. J.; Triggle, D. D. Adv. Drug Res. 1987, 16, 309.
[3] Soine, T. O. J. Pharm. Sci. 1964, 53, 1543.  
[4] Mitra, A. K.; De, A.; Karchaudhuri, N.; Misra, S. K.; Mukhopadhyay, A. K. J. Indian Chem. Soc. 1998, 75, 666.
[5] Lin, Z.; Chen, W.; Zhang, X.; Gao, Y. Chin. J. Org. Chem. 2011, 31, 1905. (林志兰, 陈文秀, 张雪利, 高原. 有机化学, 2011, 31, 1905.)
[6] Yan, Sh.; Lin, J. Chin. J. Org. Chem. 2010, 30, 465. (严胜骄, 林军. 有机化学, 2010, 30, 465.)
[7] Romine, K. R.; Morris, J. K.; Howe, W. J.; Tomich, P. K.; Horng, M. M.; Chong, K. T.; Hinshaw, R. R.; Anderson, D.J.; Strohbach, J. W.; Turner, S. R.; Mizsak, S. A. J. Med. Chem. 1996, 39, 4125.  
[8] Sreenivasulu, B.; Sundaramurthy, V.; Rao, N. V. S. Proc. Ind. Acad. Sci., Sec. A , 1974, 79, 41.
[9] Wu, P.; Cai, X.-M.; Yan, C.-G. Chin. J. Appl. Chem. 2006, 23, 1377. (吴萍, 蔡习美, 颜朝国. 应用化学. 2006, 23, 1377.)
[10] Patel, A. K.; Patel,N. H.; Patel, M. A and Brahmbhatt, D. I. ARKIVOC, 2010, (xi), 28.  
[11] Verma, A. K.; Koul, S.; Kapoor, K.K.; Razdan, T. K. Aust. J. Chem., 2007, 60, 883.
[12] Zhou, J. F; Gong,G. X; An, L. T. Synlett. 2008, 3163.
[13] Zhou, J. F; Song, Y. Zh; Lv, J. Sh. Synth. Commun. 2009, 39, 1443.  
[14] Zhou, J; Gong, G.; An, L.; Sun, X.; Zhu, F. Chin. J. Org. Chem. 2009, 29, 1988. (周建峰, 贡桂霞, 安礼涛, 孙小军, 朱凤霞. 有机化学, . 2009, 29, 1988.)
[15] Olayinka, O. A. and Obinn, C. N. J. Heter. Chem., 2010, 47, 181.
文章导航

/