63581-47-5Relevant articles and documents
Regioselective C2-arylation of imidazo[4,5-b]pyridines
Macdonald, Jonathan,Oldfield, Victoria,Bavetsias, Vassilios,Blagg, Julian
, p. 2335 - 2347 (2013/04/23)
We show that N3-MEM-protected imidazo[4,5-b]pyridines undergo efficient C2-functionalisation via direct C-H arylation. Twenty-two substituted imidazo[4,5-b]pyridines are prepared and iterative, selective elaboration of functionalised imidazo[4,5-b]pyridin
Hit generation and exploration: Imidazo[4,5-b]pyridine derivatives as inhibitors of Aurora kinases
Bavetsias, Vassilios,Sun, Chongbo,Bouloc, Nathalie,Reynisson, Johannes,Workman, Paul,Linardopoulos, Spiros,McDonald, Edward
, p. 6567 - 6571 (2008/04/03)
A hit generation and exploration approach led to the discovery of 31 (2-(4-(6-chloro-2-(4-(dimethylamino)phenyl)-3H-imidazo[4,5-b]pyridin-7-yl)piperazin-1-yl)-N-(thiazol-2-yl)acetamide), a potent, novel inhibitor of Aurora-A, Aurora-B and Aurora-C kinases
Unambiguous structural assignment of monoanils obtained from 2,3-pyridinediamines
Dubey,Kumar, R. Vinod,Kulkarni, Subhash M.,Sunder, G. Hema,Smith, Graham,Kennard, Collin H. L.
, p. 952 - 956 (2007/10/03)
The reaction of 2,3-pyridinediamine la and its 5-bromo analogue lb independently with aromatic aldehydes results in the formation of 2-amino-and 5-bromo-2-amino-3-arylideneaminopyridines (2a and 2b) respectively. The structure of 2 has been confirmed by single crystal X-ray analysis, thereby ruling out the alternate structure for these compounds.
