4.4 Article

First Synthesis of 3-Amino-2-arylimidazo[1,2-b]pyridazines by Groebke-Blackburn Reaction

Journal

SYNLETT
Volume -, Issue 12, Pages 1740-1744

Publisher

GEORG THIEME VERLAG KG
DOI: 10.1055/s-0030-1260940

Keywords

multicomponent reaction; Groebke-Blackburn reaction; heterocycles; imidazopyridazines; ring closure

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The Groebke-Blackburn transformation of an 3-aminopyridazine, a benzaldehyde, and an isocyanide allows the onestep assembly of so far unknown 3-amino-2-arylimidazo[1,2-b]pyridazines. Diversely substituted aldehydes and isocyanides can be used for this reliable three-component condensation, delivering biheterocyclic products with a broad range of different substituents in the imidazole moiety.

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