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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256599Generated: October 31, 2026

Sodium Thiosulfate → HCID 66612071, compound

https://huagongshe.com/reaction/1256599

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 66611813HCID 66611813—
SolventChloroformHCID 6212—
ProductHCID 66612071HCID 66612071—

Reaction Steps

To a mixture of 0.60 g of 1-methyl-2-(3-methylthiopyridin-4-yl)-5-trifluoromethyl-1H-benzimidazole and 9 ml of chloroform was added 1.40 g of 69% m-chloroperbenzoic acid under ice cool, then, the mixture was stirred for 2 hours at room temperature. Thereafter, a saturated sodium hydrogen carbonate aqueous solution and a saturated sodium thiosulfate aqueous solution were poured, and the mixture was extracted three times with chloroform. The combined organic layers were dried over magnesium sulfate, then, concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 0.52 g of 2-(3-methanesulfonylpyridin-4-yl)-1-methyl-5-trifluoromethyl-1H-benzimidazole (hereinafter, referred to as present active compound 19).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461181B2
Source datasetuspto-grants-2013_06
ORD IDord-4b80650378794d3b8778edee4d120548
Source noteuspto-grants-2013_06