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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713661Generated: November 4, 2026

Sodium Thiosulfate → HCID 118113337, compound

https://huagongshe.com/reaction/713661

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 118113334HCID 118113334—
SolventChloroformHCID 6212—
ProductHCID 118113337HCID 118113337—

Reaction Steps

0.18 g of m-chloroperbenzoic acid (purity of 68%) was added to a mixture of 0.12 g of 3-ethylsulfanyl-N-methyl-N-(5-pentafluoroethylpyridin-2-yl)picolinamide (Compound of Present Invention 31) and 5 mL of chloroform under ice cooling, and the mixture was stirred at room temperature for 3 hours. A saturated aqueous sodium bicarbonate solution and a saturated aqueous sodium thiosulfate solution were poured to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and then concentrated under reduced pressure, and the resulting residue was applied to a silica gel column chromatography to obtain 0.13 g of 3-ethylsulfonyl-N-methyl-N-(5-pentafluoroethylpyridin-2-yl) picolinamide (hereinafter, referred to as Compound of Present Invention 30).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09185910B2
Source datasetuspto-grants-2015_11
ORD IDord-56754e9ca2664b1ba051be1883970458
Source noteuspto-grants-2015_11