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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606262Generated: October 29, 2026

Sodium Thiosulfate → HCID 22248470, compound

https://huagongshe.com/reaction/606262

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant3-(4-(2-fluorobenzylthio)piperidino]methyl-1H-pyrazin-2-oneHCID 22248519—
SolventDichloromethaneHCID 6344—
ProductHCID 22248470HCID 2224847027%

Reaction Steps

After dissolving 57 mg of 3-[4-(2-fluorobenzylthio)piperidino]methyl-1H-pyrazin-2-one in 3 ml of dichloromethane, 31 mg of 3-chloroperbenzoic acid was added at below −70° C., the mixture was stirred for 30 minutes, and then an additional 5 mg of 3-chloroperbenzoic acid was added and the stirring was continued for 20 minutes. Aqueous sodium thiosulfate solution was added to the reaction solution and extraction was performed with dichloromethane. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (solvent: chloroform/methanol/ammonia water) to obtain the title compound (16 mg, 27% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915274B2
Source datasetuspto-grants-2011_03
ORD IDord-0bf441effb6147f18368eef1b32b9ec4
Source noteuspto-grants-2011_03