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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390473Generated: November 2, 2026

Sodium Thiosulfate → HCID 66612071, compound

https://huagongshe.com/reaction/2390473

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 numberUS08273764B2
Source datasetuspto-grants-2012_09
ORD IDord-e03bec67f0324d9386f983613aec62e3
Source noteuspto-grants-2012_09