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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1619699Generated: October 30, 2026

Cesium fluoride → 6-Chloro-3'-fluoro-4-(pyridazin-4-yl)biphenyl-3-ol

https://huagongshe.com/reaction/1619699

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium fluorideHCID 25953—
Reactant4-(Tributylstannyl)pyridazineHCID 6409733—
Reactant6-Chloro-3'-fluoro-4-iodobiphenyl-3-olHCID 58042308—
CatalystCopper iodideHCID 83717—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product6-Chloro-3'-fluoro-4-(pyridazin-4-yl)biphenyl-3-olHCID 13620087785.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

Caesium fluoride (219 mg, 1.44 mmol) was added to a solution of 6-chloro-3′-fluoro-4-iodobiphenyl-3-ol (Preparation 99, 251 mg, 0.72 mmol) and 4-(tributylstannyl)pyridazine (345 mg, 0.93 mmol) in acetonitrile (5 mL). The reaction mixture was degassed and copper iodide (28 mg, 0.15 mmol) and tetrakistriphenylphosphinepalladium (0) (83 mg, 0.07 mmol) were added. The reaction mixture was stirred at 80° C. for 3 hours. The cooled reaction mixture was diluted with ethyl acetate (20 mL) and quenched with a solution of ammonia (10%, 10 mL) and stirred for a further 10 minutes. The organic layer was separated and washed with brine (1×10 mL), dried over MgSO4, filtered and concentrated in vacuo. The residue was purified using silica gel chromatography (Biotage) eluting with heptane:ethyl acetate (93:7 to 0:100) to give the title compound (185 mg, 62%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772293B2
Source datasetuspto-grants-2014_07
ORD IDord-b9c241deedde462cbf745ecbe0469d05
Source noteuspto-grants-2014_07