Synthesis 2005(16): 2673-2676  
DOI: 10.1055/s-2005-872086
PAPER
© Georg Thieme Verlag Stuttgart · New York

A Convenient Synthesis of 3-(1-Aminoalkyl)quinolin-2(1 H )-one Derivatives

Kazuhiro Kobayashi*, Yuhei Fuchimoto, Kazutaka Hayashi, Masaaki Mano, Miyuki Tanmatsu, Osamu Morikawa, Hisatoshi Konishi
Department of Materials Science, Faculty of Engineering, Tottori University, Koyama-minami, Tottori 680-8552, Japan
Fax: +81(857)315263; e-Mail: kkoba@chem.tottori-u.ac.jp;
Further Information

Publication History

Received 29 March 2005
Publication Date:
20 July 2005 (online)

Abstract

Treatment of magnesium enolates of 1-methyl-3,4-dihydroquinolin-2(1H)-ones with nitriles, followed by N-acetylation of the resulting vinylogous urea derivatives with acetic anhydride/pyridine and double bond migration with 1,8-diazabicyclo[5.3.0]undec-7-ene, affords 3-[1-(acetylamino)alkyl]-1-methylquinolin-2(1H)-one derivatives in reasonable overall yields.

    References

  • 1a DeVita RJ. Walsh TF. Young JR. Jiang J. Ujjainwalla F. Toupence RB. Parikh M. Huang SX. Fair JA. Goulet MT. Wyvratt MJ. Lo J.-L. Ren N. Yudkovitz JB. Yang YT. Cheng K. Cui J. Mount G. Rohrer SP. Schaeffer JM. Rohdes L. Drisko JE. McGowan E. Macintyre DE. Vincent S. Carlin JR. Cameron J. Smith RG. J. Med. Chem.  2001,  44:  917 
  • 1b Hewawasam P. Fan W. Knipe J. Moon SL. Boissard CG. Gribkoff VK. Starrett JE. Lodge NJ. Bioorg. Med. Chem. Lett.  2002,  12:  1779 
  • 1c Angibaud P. Bourdrez X. Devine A. End DW. Freyne E. Lingy Y. Muller P. Mannens G. Pilatte I. Poncelet V. Skrzat S. Smets G. Dun JV. Remoortere PV. Venet M. Wouters W. Bioorg. Med. Chem. Lett.  2003,  13:  1543 
  • 1d Hewawasam P. Fan W. Ding M. Cook D. Goggins GD. Mters RA. Gribkoff VK. Boissard CG. Dworetzky SI. Starrett JE. Lodge NJ. J. Med. Chem.  2003,  46:  2819 
  • 1e Jiang J. DeVita RJ. Goulet MT. Wyvratt MJ. Lo J.-L. Ren N. Yudkovitz JB. Cui J. Yang YT. Cheng K. Rohrer SP. Bioorg. Med. Chem. Lett.  2004,  14:  1795 
  • 1f Marcaccini S. Pepino R. Pozo MC. Basurto S. García-Valverde M. Torroba T. Tetrahedron Lett.  2004,  45:  3999 
  • 1g Hewawasam P. Fan W. Cook DA. Newberry KS. Boissard CG. Gribkoff VK. Starrett JE. Lodge NJ. Bioorg. Med. Chem. Lett.  2004,  14:  4479 
  • 1h DeVita RJ. Parikh M. Jiang J. Fair JA. Young JR. Walsh TF. Goulet MT. Lo J.-L. Ren N. Yudkovitz JB. Cui J. Yang YT. Cheng K. Rohrer SP. Wyvratt MJ. Bioorg. Med. Chem. Lett.  2004,  14:  5599 ; and references cited therein
  • See, e.g.:
  • 2a Asherson JL. Young DW. J. Chem. Soc., Chem. Commun.  1977,  916 
  • 2b Jha IS. Kanth AK. Singh L. Orient. J. Chem.  1998,  14:  489 ; Chem. Abstr. 1999, 130, 281972h
  • 3a Hiyama T. Kobayashi K. Tetrahedron Lett.  1982,  23:  1597 
  • 3b Kobayashi K. Suginome H. Bull. Chem. Soc. Jpn.  1986,  59:  2635 
  • 3c Hiyama T. Kobayashi K. Nishide K. Bull. Chem. Soc. Jpn.  1987,  60:  2127 
  • 3d Kobayashi K. Kanno Y. Seko S. Suginome H. J. Chem. Soc., Chem. Commun.  1992,  780 
  • 4 Kobayashi K. Kitamura T. Nakahashi R. Shimizu A. Morikawa O. Konishi H. Heterocycles  2000,  53:  1021 
  • For other recent reports from our laboratory on the heterocycle synthesis utilizing magnesium enolates, see:
  • 5a Kobayashi K. Takabatake H. Kitamura T. Morikawa O. Konishi H. Bull. Chem. Soc. Jpn.  1997,  70:  1697 
  • 5b Kobayashi K. Nakahashi R. Shimizu A. Kitamura T. Morikawa O. Konishi H. J. Chem. Soc., Perkin Trans. 1  1999,  1747 
  • 5c Kobayashi K. Matoba T. Irisawa S. Takanohashi A. Tanmatsu M. Morikawa O. Konishi H. Bull. Chem. Soc. Jpn.  2000,  73:  2805 
  • 5d Kobayashi K. Nakashima T. Mano M. Morikawa O. Konishi H. Chem. Lett.  2001,  602 
  • 5e Kobayashi K. Nakahashi R. Mano M. Morikawa O. Konishi H. Bull. Chem. Soc. Jpn.  2003,  76:  1257 
  • 5f Kobayashi K. Honma K. Kondo S. Morikawa O. Konishi H. Heterocycles  2005,  65:  619 ; and references cited therein
  • 6 2,3-Dihydroquinolin-2(1H)-one was commercially available and the others were prepared by the procedure reported in the following paper: Guaruna A. Machetti F. Occhiato EG. Scarpi D. J. Med. Chem.  2000,  43:  3718 
  • 7 Morfat A. Carta M. Synthesis  1987,  515 
  • 8 Venkov AP. Statkova-Abeghe SM. Tetrahedron  1996,  52:  1451