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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1473923Generated: October 31, 2026

Sodium Thiosulfate → HCID 86725170, compound

https://huagongshe.com/reaction/1473923

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86725168HCID 86725168—
SolventChloroformHCID 6212—
ProductHCID 86725170HCID 86725170—

Reaction Steps

To a mixture of 2-(3-ethylsulfanyl-5-trifluoromethylpyridin-2-yl)-3-methyl-6-trifluoromethyl-3H-imidazo[4,5-b]pyridine (0.61 g) and chloroform (10 ml) was added m-chloroperbenzoic acid (purity: not less than 65%) (0.66 g) while ice-cooling, and the mixture was stirred at room temperature for 10 hours. To the reaction mixture were added aqueous 10% sodium thiosulfate solution and saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with chloroform. The organic layer was washed with water, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to give 2-(3-ethylsulfonyl-5-trifluoromethylpyridin-2-yl)-3-methyl-6-trifluoromethyl-3H-imidazo[4,5-b]pyridine (0.62 g), which is hereinafter referred to as “the present compound 5”.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018134B2
Source datasetuspto-grants-2015_04
ORD IDord-08982c3ae67742e7a8ba57b4fcf7045f
Source noteuspto-grants-2015_04