Title of article
Efficient synthesis of arylsulfamides by reaction of amines with arylsulfamoyl imidazolium triflate
Author/Authors
Lee، نويسنده , , Hyeon Kyu and Bang، نويسنده , , Miyeon and Pak، نويسنده , , Chwang Siek Pak، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2005
Pages
4
From page
7139
To page
7142
Abstract
Arylsulfamoyl imidazolium triflates, readily prepared from the corresponding chlorides, react with amines under neutral conditions to form arylsulfamides in high yields. This methodology, which contrasts with the slow and inefficient reactions of amines with arylsulfamoyl chlorides, is applied to the synthesis of arylsulfamide 3a, a bioisotere of muraglitazar.
Keywords
PPAR agonist , Arylsulfamoyl chloride , Arylsulfamide , Arylsulfamoyl imidazolium triflate
Journal title
Tetrahedron Letters
Serial Year
2005
Journal title
Tetrahedron Letters
Record number
1846908
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