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PVC-supported ethylenediamine-copper(II) complex: a heterogeneous, efficient, and eco-friendly catalyst for multi-component synthesis of 1,2,3-triazoles by reaction of propargyl bromide, aromatic azides, and amines in water

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Abstract

The PVC-supported ethylenediamine-copper(II) complex (PVC–EDA–Cu+2) has provided a highly efficient, active, and reusable heterogeneous catalyst for click chemistry. In this work, the PVC–EDA–Cu+2 catalyst is readily prepared by the reaction of PVC, ethylenediamine, and CuCl2·2H2O in water. The structure of the catalyst is then characterized via different analytical tools. This catalytic system shows a high activity in the multi-component synthesis of 1,4-disubstituted 1,2,3-triazoles by the click reaction of propargyl bromide, aromatic azides, and amines at room temperature. The advantages of this method are high reaction yield, short reaction time, and capability of recovering and reusing the catalyst. In addition, water, as a green medium, is used not only in the synthesis of 1,2,3-triazoles but also in the preparation of the catalyst. A number of new 1,2,3-triazole derivatives are also screened against two Gram-positive and Gram-negative bacterial strains.

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References

  1. H.C. Kolb, M. Finn, K.B. Sharpless, Angew. Chem. Int. Ed. 40, 11 (2001)

    Google Scholar 

  2. M. Meldal, C.W. Tornøe, Chem. Rev. 108, 8 (2008)

    Article  Google Scholar 

  3. C.W. Tornøe, C. Christensen, M. Meldal, J. Org. Chem. 67, 9 (2002)

    Article  Google Scholar 

  4. V.V. Rostovtsev, L.G. Green, V.V. Fokin, K.B. Sharpless, Angew. Chem. 114, 14 (2002)

    Article  Google Scholar 

  5. D. Dheer, R.K. Rawal, V. Singh, P. Sangwan, P. Das, R. Shankar, Tetrahedron 4295, 73 (2017)

    Google Scholar 

  6. P. Wu, V.V. Fokin, Aldrichim. Acta 40, 1 (2007)

    Google Scholar 

  7. S. Wacharasindhu, S. Bardhan, Z.-K. Wan, K. Tabei, T.S. Mansour, J. Am. Chem. Soc. 131, 12 (2009)

    Article  Google Scholar 

  8. Y. Liu, W. Yan, Y. Chen, J.L. Petersen, X. Shi, Org. Lett. 10, 23 (2008)

    CAS  Google Scholar 

  9. A.R. Katritzky, S. Bobrov, K. Kirichenko, Y. Ji, P.J. Steel, J. Org. Chem. 68, 14 (2003)

    Google Scholar 

  10. H. Nandivada, X. Jiang, J. Lahann, Adv. Mater. 19, 17 (2007)

    Article  Google Scholar 

  11. P. Wu, A.K. Feldman, A.K. Nugent, C.J. Hawker, A. Scheel, B. Voit, J. Pyun, J.M. Fréchet, K.B. Sharpless, V.V. Fokin, Angew. Chem. 116, 30 (2004)

    Article  Google Scholar 

  12. V. Aucagne, K.D. Hänni, D.A. Leigh, P.J. Lusby, D.B. Walker, J. Am. Chem. Soc. 128, 7 (2006)

    Google Scholar 

  13. M.J. Genin, D.A. Allwine, D.J. Anderson, M.R. Barbachyn, D.E. Emmert, S.A. Garmon, D.R. Graber, K.C. Grega, J.B. Hester, D.K. Hutchinson, J. Med. Chem. 43, 5 (2000)

    Google Scholar 

  14. R. Alvarez, S. Velazquez, A. San-Felix, S. Aquaro, E.D. Clercq, C.-F. Perno, A. Karlsson, J. Balzarini, M.J. Camarasa, J. Med. Chem. 37, 24 (1994)

    Article  Google Scholar 

  15. D. Dheer, V. Singh, R. Shankar, Bioorg. Chem. 30, 71 (2017)

    Google Scholar 

  16. A. Emileh, F. Tuzer, H. Yeh, M. Umashankara, D.R. Moreira, J.M. LaLonde, C.A. Bewley, C.F. Abrams, I.M. Chaiken, Biochemistry 52, 13 (2013)

    Article  Google Scholar 

  17. A.E. Wendlandt, A.M. Suess, S.S. Stahl, Angew. Chem. Int. Ed. 50, 47 (2011)

    Article  Google Scholar 

  18. M.E. Crivello, C.F. Pérez, S.N. Mendieta, S.G. Casuscelli, G.A. Eimer, V.R. Elías, E.R. Herrero, Catal. Today 133 (2008)

  19. B. Hu, Y. Yamaguchi, K. Fujimoto, Catal. Commun. 10, 12 (2009)

    Google Scholar 

  20. P. Appukkuttan, W. Dehaen, V.V. Fokin, E. Van der Eycken, Org. Lett. 6, 23 (2004)

    Article  Google Scholar 

  21. L.S. Campbell-Verduyn, L. Mirfeizi, R.A. Dierckx, P.H. Elsinga, B.L. Feringa Chem. Commun. 16 (2009)

  22. Q. Wang, T.R. Chan, R. Hilgraf, V.V. Fokin, K.B. Sharpless, M. Finn, J. Am. Chem. Soc. 125, 11 (2003)

    Google Scholar 

  23. F. Himo, T. Lovell, R. Hilgraf, V.V. Rostovtsev, L. Noodleman, K.B. Sharpless, V.V. Fokin, J. Am. Chem. Soc. 127, 1 (2005)

    Article  Google Scholar 

  24. B.R. Buckley, R. Butterworth, S.E. Dann, H. Heaney, E.C. Stubbs, ACS Catal. 5, 2 (2014)

    Google Scholar 

  25. A.K. Feldman, B. Colasson, V.V. Fokin, Org. Lett. 6, 22 (2004)

    Google Scholar 

  26. P. Siemsen, R.C. Livingston, F. Diederich, Angew. Chem. Int. Ed. 39, 15 (2000)

    Article  Google Scholar 

  27. M. Meldal, C.W. Tornøe, Chem. Rev. 108, 8 (2008)

    Article  Google Scholar 

  28. M.E. Letelier, S. Sánchez-Jofré, L. Peredo-Silva, J. Cortés-Troncoso, P. Aracena-Parks, Chem. Biol. Interact. 188, 1 (2010)

    Article  Google Scholar 

  29. R. Hudson, C.-J. Li, A. Moores, Green Chem. 14, 3 (2012)

    Article  Google Scholar 

  30. K. Jacob, A. Stolle, B. Ondruschka, K.D. Jandt, T.F. Keller, Appl. Catal. A Gen. 451 (2013)

  31. S. Chassaing, A. Sani Souna Sido, A. Alix, M. Kumarraja, P. Pale, J. Sommer, Chem. A Eur. J. 14, 22 (2008)

    Article  Google Scholar 

  32. C. Girard, E. Önen, M. Aufort, S. Beauvière, E. Samson, J. Herscovici, Org. Lett. 8, 8 (2006)

    Article  Google Scholar 

  33. T. Miao, L. Wang, Synthesis 363 (2008)

  34. B.H. Lipshutz, B.R. Taft, Angew. Chem. 118, 48 (2006)

    Google Scholar 

  35. M.L. Kantam, V.S. Jaya, B. Sreedhar, M.M. Rao, B. Choudary, J. Mol. Catal. A Chem. 256, 1 (2006)

    Article  Google Scholar 

  36. K. Yamaguchi, T. Oishi, T. Katayama, N. Mizuno, Chem. A Eur. J. 15, 40 (2009)

    Article  Google Scholar 

  37. P. Siemsen, R.C. Livingston, F. Diederich, Angew. Chem. Int. Ed. 39, 15 (2000)

    Article  Google Scholar 

  38. S. Adimurthy, C.C. Malakar, U. Beifuss, J. Org. Chem. 74, 15 (2009)

    Article  Google Scholar 

  39. A. Keivanloo, M. Bakherad, B. Bahramian, M. Rahmani, S.A.N. Taheri, Synthesis 2011 (2011)

  40. M. Bakherad, A. Keivanloo, B. Bahramian, S. Jajarmi, Appl. Catal. A 390, 1 (2010)

    Article  Google Scholar 

  41. A. Keivanloo, M. Bakherad, S.A.N. Taheri, S. Samangooei, C. R. Chim. 16, 3 (2013)

    Article  Google Scholar 

  42. M. Bakherad, A. Keivanloo, S. Samangooei, Tetrahedron Lett. 53, 43 (2012)

    Google Scholar 

  43. R. Slimi, R. Ben Othman, N. Sleimi, A. Ouerghui, C. Girard, Polymers 187, 8 (2016)

    Google Scholar 

  44. Y. Zhang, Z. Zhang, Y. Chen, Y. Li, Res. Chem. Intermed. 7307, 43 (2017)

    Google Scholar 

  45. X.-L. Shi, Q. Hu, F. Wang, W. Zhang, P. Duan, J. Catal. 233, 337 (2016)

    Google Scholar 

  46. A. Singh, M. Rawat, C. Pande, J. Appl. Polym. Sci. 876, 118 (2010)

    Google Scholar 

  47. G.R. Krishnan, K.S. Niveditha, K. Sreekumar, Indian J. Chem. 428, 52B (2013)

    Google Scholar 

  48. B. Balakrishnan, D. Kumar, Y. Yoshida, A. Jayakrishnan, Biomaterials 3495, 26 (2005)

    Google Scholar 

  49. L. Shao, C. Qi, X.-M. Zhang, RSC Adv. 53105, 4 (2014)

    Google Scholar 

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Acknowledgement

The authors wish to express their thanks to the Research Council of Shahrood University of Technology for the financial support of this research work.

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Correspondence to Ali Keivanloo.

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Keivanloo, A., Bakherad, M., Khosrojerdi, M. et al. PVC-supported ethylenediamine-copper(II) complex: a heterogeneous, efficient, and eco-friendly catalyst for multi-component synthesis of 1,2,3-triazoles by reaction of propargyl bromide, aromatic azides, and amines in water. Res Chem Intermed 44, 2571–2583 (2018). https://doi.org/10.1007/s11164-017-3247-2

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