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
Link To Document :
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