Synthesis 2017; 49(16): 3794-3800
DOI: 10.1055/s-0036-1588426
paper
© Georg Thieme Verlag Stuttgart · New York

Synthesis of [1]Benzothieno[2,3-b]quinolines via Transition-Metal-Free [3+3] Annulation of Nitroarenes and Benzo[b]thiophen-3-ylacetonitrile or 3-(Phenylsulfonylmethyl)benzo[b]thiophene Carbanions

Michał Nowacki
Institute of Organic Chemistry, Polish Academy of Sciences, ul. Kasprzaka 44/52, 01-224 Warszawa, Poland   Email: krzysztof.wojciechowski@icho.edu.pl
,
Krzysztof Wojciechowski*
Institute of Organic Chemistry, Polish Academy of Sciences, ul. Kasprzaka 44/52, 01-224 Warszawa, Poland   Email: krzysztof.wojciechowski@icho.edu.pl
› Author Affiliations
This work was financially supported by National Scientific Center grant No 2012/07/B/ST5/00813.
Further Information

Publication History

Received: 08 March 2017

Accepted after revision: 22 April 2017

Publication Date:
30 May 2017 (online)


Abstract

Benzo[b]thiophen-3-ylacetonitriles or 3-(phenylsulfonylmethyl)benzo[b]thiophenes react with nitrobenzene derivatives in the presence of potassium tert-butoxide and chlorotrimethylsilane to form, in good yields, 11-cyano- or 11-(phenylsulfonyl)[1]benzothieno[2,3-b]quinolines, respectively.

Supporting Information

 
  • References

    • 1a Mąkosza M. Wojciechowski K. Chem. Rev. 2004; 104: 2631
    • 1b Mąkosza M. Wojciechowski K. Top. Heterocycl. Chem. 2014; 37: 51
    • 1c Mąkosza M. Wojciechowski K. Heterocycles 2014; 88: 75
    • 2a Wróbel Z. Eur. J. Org. Chem. 2000; 521
    • 2b Wróbel Z. Synlett 2004; 1929
    • 2c Anczkiewicz K. Królikiewicz M. Wróbel Z. Wojciechowski K. Tetrahedron 2015; 71: 3924
    • 2d Bujok R. Cmoch P. Wróbel Z. Wojciechowski K. Org. Biomol. Chem. 2017; 15: 2397
  • 3 Bobin M. Kwast A. Wróbel Z. Tetrahedron 2007; 63: 11048
  • 4 Nowacki M. Wojciechowski K. RSC Adv. 2015; 5: 94296
  • 5 Nowacki M. Wojciechowski K. ChemistrySelect 2016; 1: 4886
  • 6 Klemm LH. McCoy DR. Klopfenstein CE. J. Heterocycl. Chem. 1971; 8: 383
  • 7 Benati L. Leardini R. Minozzi M. Nanni D. Spagnolo P. Zanardi G. J. Org. Chem. 2000; 65: 8669
  • 8 Bu X. Deady LW. Denny WA. Aust. J. Chem. 2000; 53: 143
  • 9 Camoutsis C. Catsoulacos P. Salem G. Terzis A. Filippakis SE. J. Heterocycl. Chem. 1981; 18: 1405
  • 10 Iaroshenko VO. Wang Y. Zhang B. Volochnyuk D. Sosnovskikh VY. Synthesis 2009; 2393
  • 11 Hayes CO. Bell WK. Cassidy BR. Willson CG. J. Org. Chem. 2015; 80: 7530
  • 12 Efange SM. N. Mash DC. Khare AB. Ouyang Q. J. Med. Chem. 1998; 41: 4486
    • 13a Wojciechowski K. Eur. J. Org. Chem. 2001; 3587
    • 13b Elferink VH. M. Bos HJ. T. J. Chem. Soc., Chem. Commun. 1985; 882