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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452771Generated: October 26, 2026

Sodium Thiosulfate → 4-(5-methyl-1,3,4-oxadiazol-2-yl)-N-[4-(methylsulfonyl)phenyl]pyridin-2-amine

https://huagongshe.com/reaction/452771

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant4-(5-methyl-1,3,4-oxadiazol-2-yl)-N-[4-(methylthio)phenyl]pyridin-2-amineHCID 68663319—
SolventDimethylacetamideHCID 31374—
Product4-(5-methyl-1,3,4-oxadiazol-2-yl)-N-[4-(methylsulfonyl)phenyl]pyridin-2-amineHCID 6866355743%

Reaction Steps

To a solution of 4-(5-methyl-1,3,4-oxadiazol-2-yl)-N-[4-(methylthio)phenyl]pyridin-2-amine (441 mg, 1.48 mmol) in N,N-dimethylacetamide (5 mL) was added m-chloroperbenzoic acid (70%, 531 mg, 2.22 mmol) at room temperature, and the resulting mixture was stirred for 1 hr. 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 water and saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by basic silica gel column chromatography (ethyl acetate) and recrystallized from hexane/tetrahydrofuran to give the title compound (213 mg, yield 43%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492378B2
Source datasetuspto-grants-2013_07
ORD IDord-14733de5b33f441881869a39470e8a0b
Source noteuspto-grants-2013_07