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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2102692Generated: November 2, 2026

Potassium Iodide → HCID 11998018, compound

https://huagongshe.com/reaction/2102692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(Bromomethyl)-2,6-dichloropyridineHCID 2781829—
ReactantHCID 57803077HCID 57803077—
SolventAcetoneHCID 180—
SolventEthyl AcetateHCID 8857—
ProductHCID 11998018HCID 11998018—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of rac-3-(3-methoxy-phenyl)-6-chloro-1,3-dihydro-indol-2-one (82 mg, 0.3 mmol) (from Example 6b supra), 4-bromomethyl-2,6-dichloro-pyridine (85.3 mg, 0.35 mmol) (Maybridge), potassium iodide (59.2 mg, 0.35 mmol) and potassium carbonate (89.2 mg, 0.645 mmol) in acetone (3 mL) was heated at 60° C. for 3 hours in a capped pressure tube. After cooling, mixture was diluted with ethyl acetate and extracted with water and brine. Aqueous layers were back washed with ethyl acetate. Organic layers were combined, dried (Na2SO4), filtered and concentrated. Residue was recrystallized from dichloromethane-hexanes to give rac-6-chloro-3-(2,6-dichloro-pyridin-4-ylmethyl)-3-(3-methoxy-phenyl)-1,3-dihydro-indol-2-one as a light brown solid. (Yield 60 mg, 45%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576082B2
Source datasetuspto-grants-2009_08
ORD IDord-04d540438bd949d6af4b5bccd7cdc8c8
Source noteuspto-grants-2009_08