• Title of article

    A new synthesis of oxcarbazepine using a Friedel–Crafts cyclization strategy

  • Author/Authors

    Kaufmann، نويسنده , , Daniel and Fünfschilling، نويسنده , , Peter C. and Beutler، نويسنده , , Ulrich and Hoehn، نويسنده , , Pascale and Lohse، نويسنده , , Olivier and Zaugg، نويسنده , , Werner، نويسنده ,

  • Issue Information
    هفته نامه با شماره پیاپی سال 2004
  • Pages
    4
  • From page
    5275
  • To page
    5278
  • Abstract
    A novel, simple, and straightforward process for the large-scale synthesis of oxcarbazepine, the active ingredient of Trileptal®, a medicine for the treatment of epilepsy, has been developed. Starting from readily available 1,3-dihydro-1-phenyl-2H-indol-2-one, a Friedel–Crafts cyclization strategy provides a direct route to the tricyclic framework of the target molecule. Crucial to the success of the strategy was the choice of the proper nitrogen-protecting group.
  • Keywords
    Friedel–Crafts acylation , Oxcarbazepine
  • Journal title
    Tetrahedron Letters
  • Serial Year
    2004
  • Journal title
    Tetrahedron Letters
  • Record number

    1842316