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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530906Generated: October 30, 2026

Sodium Thiosulfate → HCID 86725173, compound

https://huagongshe.com/reaction/530906

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86725171HCID 86725171—
SolventChloroformHCID 6212—
ProductHCID 86725173HCID 867251733%

Reaction Steps

To a mixture of 2-(3-ethylsulfanyl-pyridin-2-yl)-3-methyl-6-pentafluoroethyl-3H-imidazo[4,5-b]pyridine (254 mg) and chloroform (10 ml) was added m-chloroperbenzoic acid (purity: not less than 65%) (266 mg) while ice-cooling. The mixture was heated to room temperature and then stirred for 0.5 hours. To the mixture were poured saturated aqueous sodium hydrogen carbonate solution and saturated aqueous sodium thiosulfate solution, and the mixture was extracted with chloroform. The organic layer was dried over magnesium sulfate and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 2-(3-ethane sulfinyl-pyridin-2-yl)-3-methyl-6-pentafluoroethyl-3H-imidazo[4,5-b]pyridine (8 mg), which is hereinafter referred to as “the present compound 7”), and 2-(3-ethanesulfonyl-pyridin-2-yl)-3-methyl-6-pentafluoroethyl-3H-imidazo[4,5-b]pyridine (235 mg), which is hereinafter referred to as “the present compound 8”.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353110B2
Source datasetuspto-grants-2016_05
ORD IDord-e2e7bf2c3917451da9532cb3ab19874b
Source noteuspto-grants-2016_05