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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 918787Generated: October 31, 2026

Sodium Thiosulfate → HCID 72703862, compound

https://huagongshe.com/reaction/918787

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 72703864HCID 72703864—
SolventChloroformHCID 6212—
ProductHCID 72703862HCID 72703862—

Reaction Steps

436 mg of 3-chloroperoxybenzoic acid (purity of 65% or more) was added to a mixture of 236 mg of 2-(2-ethylsulfanyl-4-trifluoromethylphenyl)-6-trifluoromethyl-imidazo[1,2-a]pyridine and 5 ml of chloroform under ice cooling, and the mixture was stirred at room temperature for 4 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, then concentrated under reduced pressure. The resulting residue was applied to a silica gel column chromatography to obtain 122 mg of 2-(2-ethylsulfonyl-4-trifluoromethylphenyl)-6-trifluoromethyl-imidazo[1,2-a]pyridine (hereinafter, referred to as Compound of Present Invention 7).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09271500B2
Source datasetuspto-grants-2016_03
ORD IDord-17f073b2feae43b1b261f41d1a66eacb
Source noteuspto-grants-2016_03