Synthesis of Furo[2,3‑c]pyridazines via Tandem Transition-Metal Catalysis

A general and efficient catalytic approach to synthesis of the furo­[2,3-c]­pyridazine ring system is reported. Building on the easily accessible 2-bromo-3-aminopyridizinone skeleton, a tandem Sonogashira coupling–cycloisomerization provides ready access to functionalized furopyridazines. A wide functional group tolerance was observed in the tandem reaction, which proceeds in high yield in 1–3 h. The structure of the heterocyclic ring system was confirmed through single-crystal X-ray crystallography.