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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521684Generated: October 30, 2026

Sodium Thiosulfate → 6-(2-Ethylsulfonylphenyl)-2-trifluoromethylimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/521684

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant6-(2-Ethylsulfanylphenyl)-2-trifluoromethylimidazo[1,2-a]pyridineHCID 72549031—
SolventChloroformHCID 6212—
Product6-(2-Ethylsulfonylphenyl)-2-trifluoromethylimidazo[1,2-a]pyridineHCID 118205833—

Reaction Steps

220 mg of 3-chloroperbenzoic acid (purity of 65% or more) was added to a mixture of 134 mg of 6-(2-ethylsulfanylphenyl)-2-trifluoromethylimidazo[1,2-a]pyridine and 4 ml of chloroform, under ice cooling, and the mixture was stirred at room temperature for 4 hours. A 10% aqueous sodium thiosulfate solution was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was washed with a saturated aqueous sodium bicarbonate solution and dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. 93 mg of 6-(2-ethylsulfonylphenyl)-2-trifluoromethylimidazo[1,2-a]pyridine (Compound of Present invention 27) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328121B1
Source datasetuspto-grants-2016_05
ORD IDord-d3fbaa1deff74de4a37b6e599a6fe25c
Source noteuspto-grants-2016_05