Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2102700Generated: November 3, 2026

Potassium Iodide → HCID 11998152, compound

https://huagongshe.com/reaction/2102700

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(Bromomethyl)-3-chlorobenzeneHCID 69838—
ReactantHCID 57803044HCID 57803044—
SolventAcetoneHCID 180—
SolventEthyl AcetateHCID 8857—
ProductHCID 11998152HCID 11998152—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of rac-6-chloro-3-(2,6-dimethoxy-pyrimidin-4-yl)-1,3-dihydro-indol-2-one (0.23 g, 0.75 mmol) (from Example 29a supra), 3-chlorobenzyl bromide (0.19 g, 0.9 mmol) (Aldrich), potassium iodide (0.15 g, 0.9 mmol) and potassium carbonate (0.23 g, 1.66 mmol) in acetone (20 mL) was heated at 80° C. for 30 minutes. After cooling, mixture was diluted with ethyl acetate and washed with water and brine. Aqueous layers were back washed with ethyl acetate. The organic layers were combined, dried over Na2SO4 and concentrated. The residue was purified by chromatography (ethyl acetate-hexanes, 1:6, V/V) to give rac-6-chloro-3-(3-chloro-benzyl)-3-(2,6-dimethoxy-pyrimidin-4-yl)-1,3-dihydro-indol-2-one as an orange solid. (Yield 0.21 g, 65%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576082B2
Source datasetuspto-grants-2009_08
ORD IDord-7fb96862416b43a994697da63b1a2570
Source noteuspto-grants-2009_08