HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452841Generated: October 30, 2026
Sodium Thiosulfate → HCID 68663384, compound
https://huagongshe.com/reaction/452841
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 68663950 | HCID 68663950 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 68663384 | HCID 68663384 | 25% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08492378B2 |
|---|
| Source dataset | uspto-grants-2013_07 |
|---|
| ORD ID | ord-0cad309179b943e29569c1c6c7554cf0 |
|---|
| Source note | uspto-grants-2013_07 |
|---|