1033434-95-5Relevant academic research and scientific papers
Short and efficient access to imidazo[1,2-a]pyrrolo[3,2-c]pyridine derivatives
Gaumet, Vincent,Moreau, Emmanuel,Taleb, Abbass,Leal, Fernand,Neyts, Johan,Paeshuyse, Jan,Lartigue, Claire,Chavignon, Olivier,Gueiffier, Alain,Teulade, Jean-Claude,Métin, Jacques,Chezal, Jean-Michel
supporting information; experimental part, p. 6082 - 6085 (2011/01/04)
Access to N-protected or N-free imidazo[1,2-a]pyrrolo[3,2-c]pyridine derivatives as potential antiviral compounds was achieved in good yields from N-protected 7-amino-8-halo-2-methylimidazo[1,2-a]pyridines by catalytic coupling of terminal acetylenes under mild conditions using [PdCl2(PPh 3)2] or [Cu(Phen)(PPh3)2]NO 3.
IMIDAZO [1, 2-A] PYRROLO [3, 2-C] PYRIDINE COMPOUNDS USEFUL AS PESTIVIRUS INHIBITORS
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Page/Page column 28, (2010/04/30)
The present invention relates to a series of novel imidazo[1,2-α]pyrrolo[3,2-c]pyridines (or also named 6H-1,3a,6-Tri-aza-αy-indacenes) and derivatives thereof, according to formula: (I); The present invention also relates to processes for the preparation of imidazo[1,2-α]pyrrolo[3,2-c]pyridines, their use as. a, medicine, their use to treat or prevent viral infections and their use to manufacture a medicine to treat or prevent viral infections, particularly infections with viruses belonging to the family of the Flaviviridae and more preferably infections with Bovine Viral Diarrhea virus (BVDV).
