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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1479939Generated: October 28, 2026

3-Bromo-6-chloroimidazo(1,2-b)pyridazine → HCID 71491984, compound

https://huagongshe.com/reaction/1479939

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-6-chloroimidazo(1,2-b)pyridazineHCID 12872323—
ReactantHCID 131735053HCID 131735053—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventTetrahydrofuranHCID 8028—
ProductHCID 71491984HCID 7149198457.3%

Reaction Steps

In an inert atmosphere, 3.0 g (12.9 mmol) of 3-bromo-6-chloroimidazo[1,2-b]-pyridazine, 6.85 g (16.8 mmol) of the crude 2-stannylfuro[3,2-b]pyridine, 246 mg (1.29 mmol) copper (I) iodide and 453 mg (0.645 mmol) bis(triphenylphosphine) palladium(II)chloride in 100 mL of THF was stirred over night at 85° C. in a sealed pressure tube. The solvent was evaporated, the obtained solid was digested in dichloromethane/methanol and filtered off. The solid was washed with methanol and hexane to give 2 g of the title compound as solid material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409889B2
Source datasetuspto-grants-2016_08
ORD IDord-a254b561af9d40b09179aed2b539a346
Source noteuspto-grants-2016_08