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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201367Generated: October 29, 2026

Sodium Thiosulfate → HCID 117989538, compound

https://huagongshe.com/reaction/2201367

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 117989537HCID 117989537—
SolventChloroformHCID 6212—
ProductHCID 117989538HCID 117989538—

Reaction Steps

189 mg of 3-chloroperoxybenzoic acid (purity of 65% or more) was added to a mixture of 130 mg of 2-(4-ethylsulfanylpyrimidin-5-yl)-3-methyl-6-trifluoromethyl-3H-imidazo[4,5-b]pyridine and 4 ml of chloroform, then the mixture was stirred at room temperature for 8 hours. 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, and then concentrated under reduced pressure to obtain 130 mg of 2-(4-ethylsulfonylpyrimidin-5-yl)-3-methyl-6-trifluoromethyl-3H-imidazo[4,5-b]pyridine (hereinafter, referred to as Compound of Present Invention 15).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09364000B2
Source datasetuspto-grants-2016_06
ORD IDord-4da63d978c104cadab6f07f154ae77a4
Source noteuspto-grants-2016_06