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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373699Generated: October 31, 2026

Iodoethane → HCID 21075345, compound

https://huagongshe.com/reaction/1373699

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 21075346HCID 21075346—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 21075345HCID 2107534563.8%

Reaction Conditions

Temperature50 °C

Reaction Steps

In a 4 mL screw cap vial fitted with a small egg-shaped stir bar, were combined 5-fluoro-2-(4-fluoro-2-hydroxybenzoylamino)-N-(5-chloropyridin-2-yl)benzamide (200 mg, 0.49 mmol) and powdered anhydrous K2CO3 (103 mg, 0.74 mmol, 1.5 eq) in 0.5 mL of dry dimethylformamide (DMF). Ethyl iodide (115 mg, 0.74 mmol) was then added, the vial was capped, and the slurry heated to 50° C. with vigorous stirring overnight. The slurry was diluted with 20 mL water and extracted into 15 mL of dichloromethane. The organic layer was then washed with 20 mL portions of saturated NaHCO3, water, and brine; then dried over Na2SO4 and concentrated in vacuo. The residue was dissolved in a few mL of dichloromethane and purified by radial chromatography, eluting using hexanes, then 4:1 hexanes:EtOAc, to provide 135 mg (63%) of the title compound as pinkish-white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07163938B2
Source datasetuspto-grants-2007_01
ORD IDord-eb8c5ca016bf4ce7a4ffaba58c696d5b
Source noteuspto-grants-2007_01