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
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