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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272905Generated: October 31, 2026

Sodium Thiosulfate → HCID 117974257, compound

https://huagongshe.com/reaction/2272905

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 117974430HCID 117974430—
SolventChloroformHCID 6212—
ProductHCID 117974257HCID 117974257—

Reaction Steps

0.81 g of 3-chloroperoxybenzoic acid (purity of 65% or more) was added to a mixture of 0.56 g of 2-(5-ethylthiothiazol-4-yl)-3-methyl-6-trifluoromethyl-3H-imidazo[4,5-b]pyridine and 10 ml of chloroform, under ice cooling, and the mixture was stirred at room temperature for 5 hours and then allowed to stand overnight. A 10% aqueous sodium thiosulfate solution was poured into 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 0.6 g of 2-(5-ethylsulfonylthiazol-4-yl)-3-methyl-6-trifluoromethyl-3H-imidazo[4,5-b]pyridine (Compound of Present Invention (22)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120792B2
Source datasetuspto-grants-2015_09
ORD IDord-06c65b421a2440b88e125d1b5eb62a4d
Source noteuspto-grants-2015_09