HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606262Generated: October 29, 2026
Sodium Thiosulfate → HCID 22248470, compound
https://huagongshe.com/reaction/606262
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 3-(4-(2-fluorobenzylthio)piperidino]methyl-1H-pyrazin-2-one | HCID 22248519 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22248470 | HCID 22248470 | 27% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07915274B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-0bf441effb6147f18368eef1b32b9ec4 |
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| Source note | uspto-grants-2011_03 |
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