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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272897Generated: October 30, 2026

Sodium Thiosulfate → HCID 117974529, compound

https://huagongshe.com/reaction/2272897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 72203603HCID 72203603—
SolventChloroformHCID 6212—
ProductHCID 117974529HCID 117974529—

Reaction Steps

0.08 g of 3-chloroperoxybenzoic acid (purity of 65% or more) was added to a solution of 0.06 g of 2-(3-ethylthio-5-trifluoromethylthiophen-2-yl)-3-methyl-6-t rifluoromethyl-3H-imidazo[4,5,b]pyridine in 3 ml of chloroform under ice cooling, and the mixture was stirred for 2 hours and at room temperature for 1 hour. 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, then dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting residue was applied to a silica gel column chromatography to obtain 0.06 g of 2-(3-ethylsulfonyl-5-trifluoromethylthiophen-2-yl)-3-methyl-6-trifluoromethyl-3H-imidazo[4,5,b]pyridine (Compound of Present Invention (6)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120792B2
Source datasetuspto-grants-2015_09
ORD IDord-486c7fa54d08420caf22519799861b68
Source noteuspto-grants-2015_09