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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201351Generated: October 29, 2026

Sodium Thiosulfate → HCID 117988775, compound

https://huagongshe.com/reaction/2201351

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 117988884HCID 117988884—
SolventChloroformHCID 6212—
ProductHCID 117988775HCID 117988775—

Reaction Steps

542 mg of 3-chloroperoxybenzoic acid (purity of 65% or more) was added to a mixture of 416 mg of 2-(2-ethylsulfanyl-6-trifluoromethylpyridin-3-yl)-3-methyl-6-trifluoromethyl-3H-imidazo[4,5-b]pyridine and 5 ml of chloroform, and the mixture was stirred at room temperature for 1 hour, then allowed to stand at room temperature overnight. A 10% aqueous sodium thiosulfate solution was poured 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, then concentrated under reduced pressure to obtain 452 mg of 2-(2-ethylsulfonyl-6-trifluoromethylpyridin-3-yl)-3-methyl-6-trifluoromethyl-3H-imidazo[4,5-b]pyridine (hereinafter, referred to as Compound of Present Invention 5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09364000B2
Source datasetuspto-grants-2016_06
ORD IDord-52f7deaa47e9444ea88dbbedce080a03
Source noteuspto-grants-2016_06