Citation: Liu Yufeng, Cao Zhongzhong, Su Miaodong, Li Hui, Fu Meiqiang, Liu Qiang, Luo Weiping, Guo Cancheng. Iron(Ⅲ) Porphyrin Catalyzed Cyclization of Ketones with Dimethyl Sulfoxide and Ammonium Acetate: One-Pot Synthesis of Pyridines[J]. Chinese Journal of Organic Chemistry, ;2019, 39(1): 129-136. doi: 10.6023/cjoc201809014 shu

Iron(Ⅲ) Porphyrin Catalyzed Cyclization of Ketones with Dimethyl Sulfoxide and Ammonium Acetate: One-Pot Synthesis of Pyridines

  • Corresponding author: Guo Cancheng, ccguo@hnu.edu.cn
  • Received Date: 7 September 2018
    Revised Date: 29 November 2018
    Available Online: 5 January 2018

    Fund Project: the National Natural Science Foundations of China 21572049Project supported by the National Natural Science Foundations of China (No. 21572049)

Figures(2)

  • An iron(Ⅲ)-porphyrin-catalyzed cyclization of ketones with dimethyl sulfoxide (DMSO) and ammonium acetate for the synthesis of unsymmetrical and symmetrical pyridines by employing DMSO as C4 or C6 source has been developed. Various aryl ketone derivatives react readily with DMSO, producing the pyridines in yields of 30%~85%. This method uses non-noble metals and proceeds under mild reaction conditions with operational simplicity, which thus allows the expedient assembly of pyridines from readily available ketones. Based on the preliminary experiments, a plausible mechanism of this transformation is disclosed.
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    1. [1]

      (a) Eicher, T.; Hauptmann, S. The Chemistry of Heterocycles, Wiley-VCH, Weinheim, 2003.
      (b) Katritzky, A. R.; Ramsden, C. A.; Scriven, E. F. V.; Taylor, R. J. Comprehensive Heterocyclic Chemistry, Elsevier, Oxford, 2008.
      (c) Joule, J. A.; Mills, K. Heterocyclic Chemistry, Wiley, Chichester, 2010.

    2. [2]

      (a) Forbes, I. T.; Johnson, C. N.; Jones, G. E.; Loudon, J.; Nicholass, J. M.; Thompson, M.; Upton, N. J. Med. Chem. 1990, 33, 2640.
      (b) Zhmurenko, L. A.; Molodavkin, G. M.; Voronina, T. A.; Lezina, V. P. Pharm. Chem. J. 2012, 46, 15.

    3. [3]

      Bahekar, R. H.; Jain, M. R.; Jadav, P. A.; Prajapati, V. M.; Patel, D. N.; Gupta, A. A.; Sharma, A.; Tom, R.; Bandyopadhya, D.; Modi, H.; Patel, P. R. Bioorg. Med. Chem. 2007, 15, 6782.

    4. [4]

      Rival, Y.; Grassy, G.; Taudou, A.; Ecalle, R. Eur. J. Med. Chem. 1991, 26, 13.  doi: 10.1016/0223-5234(91)90208-5

    5. [5]

      Zhuravel, I. O.; Kovalenko, S. M.; Ivachtchenko, A. V.; Balakin K. V.; Kazmirchuk, V. V. Bioorg. Med. Chem. Lett. 2005, 15, 5483.  doi: 10.1016/j.bmcl.2005.08.081

    6. [6]

      (a) Musonda, C. C.; Whitlock, G. A.; Witty, M. J.; Brun, R.; Kaiser, M. Bioorg. Med. Chem. Lett. 2009, 19, 401.
      (b) Moreno, D.; Plano, D.; Baquedano, Y.; Jimeez-Ruiz, A.; Palop, J. A.; Sanmartn, C. Parasitol. Res. 2011, 108, 233.

    7. [7]

      Rupert, K. C.; Henry, J. R.; Dodd, J. H.; Wadsworth, S. A.; Cavender, D. E.; Olini, G. C.; Fahmy, B.; Siekierka, J. J. Bioorg. Med. Chem. Lett. 2003, 13, 347.  doi: 10.1016/S0960-894X(02)01020-X

    8. [8]

      Kouznetsov, V. V.; Mendez, L. Y. V.; Tibaduiza, B.; Ochoa, C.; Pereira, D. M.; Ruiz, J. J. N.; Portillo, C. F.; Serrano, S. M.; Barrio, A. G.; Bahsas, A.; Amaro-Luis, J. Arch. Pharm. Pharm. Med. Chem. 2004, 337, 127.  doi: 10.1002/(ISSN)1521-4184

    9. [9]

      (a) Gibson, V. C.; Redshaw, C.; Solan, G. A. Chem. Rev. 2007, 107, 1745.
      (b) Rycke, N. D.; Couty, F.; David, O. R. P. Chem.-Eur. J. 2011, 17, 12852.

    10. [10]

      (a) Allais, C.; Grassot, J. M.; Rodriguez, J.; Constantieux, T. Chem. Rev. 2014, 114, 10829.
      (b) Zhao, M. N.; Hui, R. R.; Ren, Z. H.; Wang, Y. Y.; Guan, Z. H. Org. Lett. 2014, 16, 3082.
      (c) Bai, Y.; Tang, L. C.; Huang, H. W.; Deng, G. J. Org. Biomol. Chem. 2015, 13, 4404.
      (d) Yan, Y. Z.; Li, H. Y.; Li, Z.; Niu, B.; Shi, M. M.; Liu, Y. Q. J. Org. Chem. 2017, 82, 8628.

    11. [11]

      (a) Meunier, B. Biomimetic Oxidations Mediated by Metal Complexes, Imperial College Press, London, 2000.
      (b) Meunier, B.; de Visser, S. P.; Shaik, S. Chem. Rev. 2004, 104, 3947.
      (c) Zhou, X. T.; Ji, H. B.; Pei, L. X.; She, Y. B.; Xu, J. C.; Wang, L. F. Chin. J. Org. Chem. 2007, 27, 1039(in Chinese).
      (周贤太, 纪红兵, 裴丽霞, 佘远斌, 徐建昌, 王乐夫, 有机化学, 2007, 27, 1039.)

    12. [12]

      (a) Collman, J. P.; Wang, Z.; Straumanis, A.; Quelquejeu, M.; Rose, E. J. Am. Chem. Soc. 1999, 121, 460.
      (b) Yu, X. Q.; Huang, J. S.; Yu, W. Y.; Che, C. M. J. Am. Chem. Soc. 2000, 122, 5337.
      (c) Au, S. M.; Huang, J. S.; Yu, W. Y.; Fung, W. H.; Che, C. M. J. Am. Chem. Soc. 1999, 121, 9120.

    13. [13]

      (a) Li, Y.; Huang, J. S.; Zhou, Z. Y.; Che, C. M. J. Am. Chem. Soc. 2001, 123, 4843.
      (b) Bartoli, J. F.; Mansuy, V. M.; Barch-Ozette, K. L.; Palacio, M.; Battioni, P.; Mansuy, D. Chem. Commun. 2000, 827.
      (c) Yang, J.; Weinberg, R.; Breslow, R. Chem. Commun. 2000, 531.
      (d) Yu, W. Y.; Huang, J. S.; Zhou, Z. Y.; Che, C. M. Org. Lett. 2000, 2, 2233.

    14. [14]

      (a) Li, Y. F.; Guo, C, C.; Yan, X. H.; Liu, Q. J. Porphyrins Phthalocyanines 2006, 10, 942.
      (b) Jiang, Q.; Sheng, W. B.; Tian, M.; Tang, J. S.; Guo, C. C. Eur. J. Org. Chem. 2013, 10, 1861.
      (c) Sheng, W. B.; Jiang, Q.; Luo, W. P.; Guo, C. C. J. Org. Chem. 2013, 78, 5691.

    15. [15]

      (a) Pan, X. J.; Liu, Q.; Chang, L. M.; Yuan, G. Q. RSC Adv. 2015, 5, 51183.
      (b) Wu, X.; Zhang, J. H.; Liu, S.; Gao, Q. H.; Wu, A. X. Adv. Synth. Catal. 2016, 358, 218.

    16. [16]

      Liu, Y. F.; Ji, P. Y.; Xu, J. W.; Hu, Y. Q.; Liu, Q.; Luo, W. P.; Guo, C. C. J. Org. Chem. 2017, 82, 7159.  doi: 10.1021/acs.joc.7b00619

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