Citation: Peng Zhao, Zi Zeng, Xiaoming Feng, Xiaohua Liu. Multisubstituted pyrazole synthesis via [3 + 2] cycloaddition/rearrangement/N—H insertion cascade reaction of α-diazoesters and ynones[J]. Chinese Chemical Letters, ;2021, 32(1): 132-135. doi: 10.1016/j.cclet.2020.11.053 shu

Multisubstituted pyrazole synthesis via [3 + 2] cycloaddition/rearrangement/N—H insertion cascade reaction of α-diazoesters and ynones

    * Corresponding authors.
    E-mail addresses: xmfeng@scu.edu.cn (X. Feng), liuxh@scu.edu.cn (X. Liu).
  • Received Date: 17 September 2020
    Revised Date: 16 November 2020
    Accepted Date: 18 November 2020
    Available Online: 30 November 2020

Figures(5)

  • The cascade reactions of alkyl α-diazoesters and ynones using Al(OTf)3 as the catalyst are described. A series of 4-substituted pyrazoles were obtained via [3 + 2] cycloaddition, 1, 5-ester shift, 1, 3-H shift, and N—H insertion process. Deuterium labelling experiments, kinetic studies and control experiments were carried out for the rationalization of the mechanism.
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    1. [1]

      (a) L.Pizzutia, A.G.Barschakb, S.Moura, etal., Curr.Org.Chem.18 (2014) 115-126;
      (b) M.S. Moreno, C. Marín, J. Pitarch, et al., J. Med. Chem. 55 (2012) 4231-4243;
      (c) A. Ansari, A. Ali, M. Asif, Shamsuzzaman, New J. Chem. 41 (2017) 16-41;
      (d) M.E. Monteiro, G. Lechuga, M.C.S. Pereira, et al., Eur. J. Med. Chem.182 (2019) 111610-111623;
      (e) M.S.D. Santos, M.L.V. Oliveira, M.M.C. Cavalheiro, et al., Bioorg. Med. Chem. Lett. 21 (2011) 7451-7454;
      (f)B.F.Ruan, Y.Z.Zhu, W.D.Liu, B.A.Song, Y.P.Tian, Eur.J.Med.Chem.72 (2014) 46-51;
      (g)M.F.Khan, M.M.Alam, M.Shaquiquzzaman, etal., Eur.J.Med.Chem.120 (2016) 170-201;
      (h) J.V. Faria, P.F. Vegi, A.M.R. Bernardino, et al., Bioorg. Med. Chem. 25 (2017) 5891-5903.

    2. [2]

      (a) L. Leroy, S. Cousin, A. Italiano, Eur. J. Cancer 81 (2017) 102-105;
      (b) J.A. Balfour, H.M. Bryson, R.N. Brogden, Drugs 51 (1996) 99-136;
      (c) M.M. Buckley, R.N. Brogden, K.L. Goa, et al., Drugs 44 (1992) 408-444;
      (d) A. Sadurn, G. Kehr, R. Gilmour, et al., Chem. Eur. J. 24 (2018) 2832-2836;
      (e) M.S. McClure, M.B. Berry, J. Powers, et al., Eur. J. Org. Chem. 19 (2012) 3561-3565;
      (f) D.W. Graham, W.T. Ashton, E.F. Rogers, et al., J. Med. Chem. 30 (1987) 1074-1090;
      (g) P.G. Middleton, M.A. Mall, R. Jain, et al., N. Engl. J. Med. 381 (2019) 1809-1819;
      (h) T. Nishina, S. Takahashi, T. Doi, et al., Invest. New Drugs 36 (2018) 424-434.

    3. [3]

      (a) S. Fustero, M.S. Rosello, P. Barrio, A.S. Fuentes, Chem. Rev. 111 (2011) 6984-7034;
      (b) K. Karrouchi, M. Ansar, et al., Molecules 23 (2018) 134-220;
      (c) J.S.S. Neto, G. Zeni, Chem. Eur. J. 26 (2020) 8175-8189;
      (d) Y.L. Janin, Chem. Rev. 112 (2012) 3924-3958;
      (e) B. Eftekhari-Sis, M. Zirak, A. Akbari, Chem. Rev. 113 (2013) 2958-3043.

    4. [4]

      (a) A. Lévai, A.M.S. Silva, J. Jeko, et al., Eur. J. Org. Chem. 12 (2006) 2825-2832;
      (b) S.K. Singh, M.S. Reddy, Y.K. Rao, et al., Tetrahedron Lett. 45 (2004) 7679-7682;
      (c) Z.X. Wang, H.L. Qin, Green Chem. 6 (2004) 90-92;
      (d) M.C. Bagley, M.C. Lubinu, C. Mason, Synlett 5 (2007) 704-708;
      (e) G. Cabarrocas, M. Ventura, J.M. Villalgordo, Tetrahedron: Asymmetry 11 (2000) 2483-2493;
      (f) D.B. Grotjahn, S. Van, L. Mejorad, et al., J. Org. Chem. 67 (2002) 9200-9209.

    5. [5]

      (a) K. Mohanan, A.R. Martin, J.J. Vasseur, et al., Angew. Chem. Int. Ed. 49 (2010) 3196-3199;
      (b) Z. Chen, Y. Zhang, J. Nie, J.A. Ma, Org. Lett. 20 (2018) 2120-2124;
      (c) P.K. Mykhailiuk, Eur. J. Org. Chem. 33 (2015) 7235-7239.

    6. [6]

      D. Drikermann, V. Kerndl, H. Görls, I. Vilotijevic, Synlett 31 (2020) 1158-1162.  doi: 10.1055/s-0040-1707111

    7. [7]

      (a) M.P. Doyle, M.A. McKervey, T. Ye, Modern Catalytic Methods for Organic Synthesis With Diazo Compounds: From Cyclopropanes to Ylides, Wiley, New York, 1998;
      (b) A. Ford, H. Miel, M.A. McKervey, et al., Chem. Rev. 115 (2015) 9981-10080.

    8. [8]

      (a) A. Padwa, W.H. Pearson, Synthetic Applications of 1, 3-Dipolar Cycloaddition Chemistry Toward Heterocycles and Natural Products, John Wiley and Sons, New York, 2002;
      (b) A. Arrieta, J.R. Carrillo, A. Morenn, et al., Tetrahedron 54 (1998) 13167-13168;
      (c) S. Kobayashi, R. Hirabayashi, Y. Yamashita, etal., Tetrahedron Lett. 44 (2003) 3351-3354;
      (d) L. Wu, M. Shi, J. Org. Chem. 75 (2010) 2296-2301;
      (e) N. Jiang, C.J. Li, Chem. Commun. (2004) 394-395;
      (f) Y. Li, L. Liu, J. Zhang, Org. Lett. 20 (2018) 6444-6448.

    9. [9]

      (a) P.R. Krishna, E.R. Sekhar, F. Mongin, Tetrahedron Lett. 49 (2008) 6768-6772;
      (b) X. Qi, J.M. Ready, Angew. Chem. Int. Ed. 46 (2007) 3242-3244;
      (c) N.A. McGrath, R.T. Raines, Chem. Sci. 3 (2012) 3237-3240;
      (d) P. Zhao, S. Wu, C. Ke, X. Liu, X. Feng, Chem. Commun. 54 (2018) 9837-9840.

    10. [10]

      X. Yi, J. Feng, F. Huang, J.B. Baell, Chem. Commun. 56 (2020) 1243-1246.  doi: 10.1039/C9CC08389H

    11. [11]

      J. Shao, W. Chen, M. Zhao, et al., Org. Lett. 20 (2018) 3992-3995.  doi: 10.1021/acs.orglett.8b01562

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