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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272899Generated: October 30, 2026

Sodium Thiosulfate → HCID 117974277, compound

https://huagongshe.com/reaction/2272899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 117974373HCID 117974373—
SolventChloroformHCID 6212—
ProductHCID 117974277HCID 117974277—

Reaction Steps

0.08 g of 3-chloroperoxybenzoic acid (purity of 65% or more) was added to 3 ml of a solution of 0.07 g of 2-(2-ethylthio-5-trifluoromethylthiophen-3-yl)-3-methyl-6-pentafluoroethyl-3H-imidazo[4,5,b]pyridine in 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 0.07 g of 2-(2-ethylsulfonyl-5-trifluoromethylthiophen-3-yl)-3-methyl-6-pentafluoroethyl-3H-imidazo[4,5,b]pyridine (Compound of Present Invention (10)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120792B2
Source datasetuspto-grants-2015_09
ORD IDord-f473435004a841b0ac05f016a738be5a
Source noteuspto-grants-2015_09