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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1473929Generated: October 30, 2026

Sodium Thiosulfate → HCID 71246869, compound

https://huagongshe.com/reaction/1473929

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 71246825HCID 71246825—
SolventChloroformHCID 6212—
ProductHCID 71246869HCID 7124686967.9%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a mixture of 2-(3-ethylsulfonyl-pyridin-2-yl)-3-methyl-6-trifluoromethylsulfanyl-3H-imidazo[4,5-b]pyridine (500 mg) and chloroform (10 ml) was added m-chloroperbenzoic acid (purity: not less than 65%) (429 mg) while ice-cooling, and the mixture was stirred at room temperature for 1 hour and at 50° C. for 2 hours. To the reaction mixture were poured aqueous sodium thiosulfate solution and aqueous sodium hydrogen carbonate solution, and the mixture was extracted with chloroform. The organic layer was dried over sodium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 2-(3-ethylsulfonyl-pyridin-2-yl)-3-methyl-6-trifluoromethylsulfinyl-3H-imidazo[4,5-b]pyridine (353 mg), which is hereinafter referred to as “the present compound 20”.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018134B2
Source datasetuspto-grants-2015_04
ORD IDord-5e270535cabd4cd7861c1560e339d3e9
Source noteuspto-grants-2015_04