Synthesis 2012(12): 1792-1797  
DOI: 10.1055/s-0031-1289715
PSP
© Georg Thieme Verlag Stuttgart ˙ New York

Copper-Catalyzed Direct Amination of Polyfluoroarenes and Azoles with Hydroxylamines and Its Application to the Synthesis of 3-Aminobenzoheteroles

Naoki Matsuda, Koji Hirano*, Tetsuya Satoh, Masahiro Miura*
Department of Applied Chemistry, Faculty of Engineering, Osaka University, Suita, Osaka 565-0871, Japan
Fax: +81(6)68797362; e-Mail: k_hirano@chem.eng.osaka-u.ac.jp; miura@chem.eng.osaka-u.ac.jp;
Further Information

Publication History

Received 9 January 2012
Publication Date:
15 February 2012 (online)

Abstract

A copper-catalyzed electrophilic, umpolung amination strategy for the direct C-H amination of polyfluoroarenes and 1,3-azoles has been developed. The copper-based amination reaction is robust and can be easily scaled up on a gram scale. Its application to an annulative electrophilic amination of o-alkynylphenols and -anilines for the synthesis of 3-aminobenzofurans and -indoles is also described.

    References

  • 1a Hili R. Yudin AK. Nat. Chem. Biol.  2006,  2:  284 
  • 1b Amino Group Chemistry: From Synthesis to the Life Sciences   Ricci A. Wiley-VCH; Weinheim: 2007. 
  • Reviews:
  • 2a Muci AR. Buchwald SL. Top. Curr. Chem.  2002,  219:  131 
  • 2b Hartwig JF. Acc. Chem. Res.  2008,  41:  1534 
  • 2c Surry DS. Buchwald SL. Angew. Chem. Int. Ed.  2008,  47:  6338 
  • Reviews:
  • 3a Ley SV. Thomas AW. Angew. Chem. Int. Ed.  2003,  42:  5400 
  • 3b Monnier F. Taillefer M. Angew. Chem. Int. Ed.  2009,  48:  6954 
  • 4a Berman AM. Johnson JS. J. Am. Chem. Soc.  2004,  126:  5680 
  • 4b Berman AM. Johnson JS. J. Org. Chem.  2006,  71:  219 
  • 5a Matsuda N. Hirano K. Satoh T. Miura M. Org. Lett.  2011,  13:  2860 
  • For a relevant amination with a chloroamine, see:
  • 5b Kawano T. Hirano K. Satoh T. Miura M. J. Am. Chem. Soc.  2010,  132:  6900 
  • 6a Hirano K. Satoh T. Miura M. Org. Lett.  2011,  13:  2395 
  • 6b Matsuda N. Hirano K. Satoh T. Miura M. J. Org. Chem.  2012,  77:  617 
  • 7 Shen K. Fu Y. Li J.-N. Liu L. Guo Q.-X. Tetrahedron  2007,  63:  1568 
  • 8a Jaime-Figueroa S. Liu Y. Muchowski JM. Putman DG. Tetrahedron Lett.  1998,  39:  1313 
  • 8b Cadierno V. García-Garrido SE. Gimeno J. Nebra N. Chem. Commun.  2005,  4086 
  • 9 Do H.-Q. Khan RMK. Daugulis O. J. Am. Chem. Soc.  2008,  130:  15185 
  • 10 For a relevant heterocycle synthesis based on a similar concept, see: Hiroya K. Itoh S. Sakamoto T. J. Org. Chem.  2004,  69:  1126 
  • 11a Lehmann F. Haile S. Axen E. Medina C. Uppenberg J. Svensson S. Lundbaeck T. Rondahl L. Barf T. Bioorg. Med. Chem. Lett.  2004,  14:  4445 
  • 11b Bahekar RH. Jain MR. Goel A. Patel DN. Prajapati VM. Gupta AA. Jadav PA. Patel PR. Bioorg. Med. Chem.  2007,  15:  3248 
  • 11c Romagnoli R. Baraldi PG. Sarkar T. Carrion MD. Cara CL. Cruz-Lopez O. Preti D. Tabrizi MA. Tolomeo M. Grimaudo S. Di Christina A. Zonta N. Balzarini J. Brancale A. Hseih H.-P. Hamel E. J. Med. Chem.  2008,  51:  1464 
  • Selected work:
  • 12a Chen X. Hao X.-S. Goodhue CE. Yu J.-Q. J. Am. Chem. Soc.  2006,  128:  6790 
  • 12b Uemura T. Imoto S. Chatani N. Chem. Lett.  2006,  35:  842 
  • 12c Monguchi D. Fujiwara T. Furukawa H. Mori A. Org. Lett.  2009,  11:  1607 
  • 12d Wang Q. Schreiber SL. Org. Lett.  2009,  11:  5178 
  • 12e Shuai Q. Deng G. Chua Z. Bohle DS. Li C.-J. Adv. Synth. Catal.  2010,  352:  632 
  • 12f Zhao H. Wang M. Su W. Hong M. Adv. Synth. Catal.  2010,  352:  1301 
  • 12g John A. Nicholas KM. J. Org. Chem.  2011,  76:  4158 
  • 13 Yoneda E. Sugioka T. Hirao K. Zhang SW. Takahashi S. J. Chem. Soc., Perkin Trans. 1  1998,  477