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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437291Generated: November 1, 2026

Sodium Thiosulfate → HCID 57940688, compound

https://huagongshe.com/reaction/1437291

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 57940615HCID 57940615—
SolventDichloromethaneHCID 6344—
ProductHCID 57940688HCID 57940688—

Reaction Steps

At 0° C., 3-chloroperbenzoic acid (0.260 g) was added to a solution of 4-[1-(6-methoxy-3-pyridyl)-5-(4-methylthio-2-pyridyl)pyrazole-3-carbonyl]piperazine-1-carboxylic acid tert-butyl ester (0.366 g) obtained in Example 47 in methylene chloride (7.3 mL), and the mixture was stirred for 20 minutes. Subsequently, the mixture was stirred at room temperature for a further 2 hours. At 0° C., 3-chloroperbenzoic acid (0.124 g) was added thereto, and the resultant mixture was stirred for 2 hours. Saturated aqueous sodium thiosulfate (10 mL) and saturated aqueous sodium hydrogencarbonate (10 mL) were added to the reaction mixture, followed by stirring. The reaction mixture was partitioned between water and chloroform. The organic layer was dried over sodium sulfate anhydrate. After filtration, the solvent was removed under reduced pressure. The residue was purified through silica gel column chromatography (chloroform-methanol), to thereby give the title compound as an amorphous product (0.387 g, 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622471B2
Source datasetuspto-grants-2009_11
ORD IDord-03db52cf3c6f430dba8e7930b29be409
Source noteuspto-grants-2009_11