Title of article :
New and Efficient Synthesis oflmidazo[4,5-b]pyridine-5-ones
Author/Authors :
Zaki، Magdi E. A. نويسنده , , Proenca، M. Fernanda نويسنده , , Booth، Brian L. نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2005
Pages :
-2428
From page :
2429
To page :
0
Abstract :
l-Aryl-5-amino-4-cyanoformimidoylimidazoles 1 were reacted with methyl cyanoacetate, under mild experimental conditions, leading to 3-aryl-6,7-dicyanoimidazo[4,5-b]pyridine-5-ones 5, isolated after neutralization of their ammonium salts 4. A reaction intermediate, imidazole 3d, the precursor of the bicyclic structure 5d, could be isolated under carefully controlled experimental conditions and was shown to cyclize to imidazo[4,5-b]pyridine-5-one (4d, isolated as the DBU salt) after reflux in ethanol, in the presence of DBU.
Keywords :
neighboring-group effect , imidazole , nitriles , Heterocycles , diaminomaleonitrile
Journal title :
Synlett
Serial Year :
2005
Journal title :
Synlett
Record number :
110826
Link To Document :
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