Synthesis 2011(3): 409-412  
DOI: 10.1055/s-0030-1258376
PAPER
© Georg Thieme Verlag Stuttgart ˙ New York

An Improved Synthesis of Phenylethynyl[1,2,4]methyltriazines

Jeremy P. Olson, F. Ivy Carroll*
Center for Organic and Medicinal Chemistry, Research Triangle Institute, Research Triangle Park, NC, 27709, USA
Fax: +1(919)5418868; e-Mail: fic@rti.org;
Further Information

Publication History

Received 22 September 2010
Publication Date:
20 December 2010 (online)

Abstract

An improved synthesis of phenylethynyl[1,2,4]methyltriazines is described. In this method, 5-methyl-3-methyl­thio[1,2,4]triazine is cross-coupled with various phenylacetylenes using microwave conditions to produce phenylethynyl[1,2,4]methyltriazines in increased yields. Interest in the phenylethynyl[1,2,4]methyltriazine scaffold stems from recent reports demonstrating their potency as mGluR5 antagonists.

    References

  • 1 Carroll FI. Kotturi SV. Navarro HA. Mascarella SW. Gilmour BP. Smith FL. Gabra BH. Dewey WL. J. Med. Chem.  2007,  50:  3388 
  • 2a Chiamulera C. Epping-Jordan MP. Zocchi A. Marcon C. Cottiny C. Tacconi S. Corsi M. Orzi F. Conquet F. Nat. Neurosci.  2001,  4:  873 
  • 2b Rasmussen K. Martin H. Berger JE. Seager MA. Neuropharmacology  2005,  48:  173 
  • 2c Ghasemzadeh MB. Nelson LC. Lu X.-Y. Kalivas PW. J. Neurochem.  1999,  72:  157 
  • 2d Freeman WM. Brebner K. Lynhc WJ. Robertson DJ. Roberts DCS. Vrana KE. Neuroscience  2001,  108:  371 
  • 3 Gabra BH. Smith FL. Navarro HA. Carroll FI. Dewey WL. Brain Res.  2008,  1187:  58 
  • 4 Carroll FI. Ann. N. Y. Acad. Sci.  2008,  1141:  211 
  • 5a Gasparini F. Lingenhohl K. Stoehr N. Flor PJ. Heinrich M. Vranesic I. Biollaz M. Allgeier H. Heckendorn R. Urwyler S. Varney MA. Johnson EC. Hess SD. Rao SP. Sacaan AI. Santori EM. Veliçelebi G. Kuhn R. Neuropharmacology  1999,  38:  1493 
  • 5b Cosford ND. Tehrani L. Roppe J. Schweiger E. Smith ND. Anderson J. Bristow L. Brodkin J. Jiand X. McDonald I. Rao S. Washburn M. Varney MAL. J. Med. Chem.  2003,  46:  204 
  • 6 Negishi EI. Anastasia L. Chem. Rev.  2003,  103:  1979 
  • 7a Liebeskind LS. Srogl J. Org. Lett.  2002,  4:  979 
  • 7b Egi M. Liebeskind L. Org. Lett.  2003,  5:  801 
  • 7c Alphonse FA. Suzenet F. Keromnes A. Lebret B. Guillaumet G. Org. Lett.  2003,  5:  803 
  • 8a Mehta VP. Sharma A. Van der Eycken E. Org. Lett.  2008,  10:  1147 
  • 8b Shook BC. Chakravarty D. Jackson PF. Tetrahedron Lett.  2009,  50:  1013