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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480202Generated: October 30, 2026

Potassium Iodide → HCID 59111303, compound

https://huagongshe.com/reaction/480202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-1-[4-(4-fluoro-benzyl)-(2R,5S)-2,5-dimethyl-piperazin-1-yl]-ethanoneHCID 11358461—
Reactant5-Chloro-2-hydroxy-N-methyl-benzenesulfonamideHCID 18768102—
SolventMethyl Ethyl KetoneHCID 6569—
SolventEthyl AcetateHCID 8857—
ProductHCID 59111303HCID 5911130353%

Reaction Steps

To a solution of (2R, 5S)-2-Chloro-1-[4-(4-fluoro-benzyl)-2,5-dimethyl-piperazin-1-yl]-ethanone (375 mg, 1.26 mmol) in butanone (12 ml) was added 5-Chloro-2-hydroxy-N-methyl-benzenesulfonamide (280 mg, 1.26 mmol), potassium carbonate (348 mg, 2.52 mmol) and potassium iodide (209 mg, 1.26 mmol). The resulting reaction mixture was refluxed for 4 hours. It was allowed to cool, diluted with ethyl acetate and washed with brine. The organic layer was separated, dried over magnesium sulfate, filtered and concentrated in vacuo. Chromatography on silica gel gave the above titled compound (320 mg, 53% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06649611B2
Source datasetuspto-grants-2003_11
ORD IDord-b94ae8813efb4a7abd959af2e8abea53
Source noteuspto-grants-2003_11