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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452841Generated: October 30, 2026

Sodium Thiosulfate → HCID 68663384, compound

https://huagongshe.com/reaction/452841

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 68663950HCID 68663950—
SolventDimethylacetamideHCID 31374—
ProductHCID 68663384HCID 6866338425%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 4-[5-(methylthio)-1,3,4-oxadiazol-2-yl]-N-[3-(trifluoromethyl)phenyl]pyridin-2-amine (455 mg, 1.29 mmol) in N,N-dimethylacetamide (5 mL) was added m-chloroperbenzoic acid (70%, 619 mg, 2.58 mmol), and the resulting mixture was stirred at room temperature for 2 hr and at 50° C. overnight. A saturated aqueous sodium thiosulfate solution was added to the reaction mixture, and the mixture was stirred for 15 min and extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=9/1-0/1) and recrystallized from hexane/ethyl acetate to give the title compound (126 mg, yield 25%) as yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492378B2
Source datasetuspto-grants-2013_07
ORD IDord-0cad309179b943e29569c1c6c7554cf0
Source noteuspto-grants-2013_07