HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521682Generated: October 29, 2026
Sodium Thiosulfate → 6-(2-ethylsulfonylphenyl)-3-methyl-2-trifluoromethyl-3H-imidazo[4,5-b]pyridine
https://huagongshe.com/reaction/521682
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 6-(2-ethylsulfanylphenyl)-3-methyl-2-trifluoromethyl-3H-imidazo[4,5-b]pyridine | HCID 118034991 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 6-(2-ethylsulfonylphenyl)-3-methyl-2-trifluoromethyl-3H-imidazo[4,5-b]pyridine | HCID 118034977 | — |
Reaction Steps
0.70 g of 3-chloroperbenzoic acid (purity of 65% or more) was added to a mixture of 0.35 g of 6-(2-ethylsulfanylphenyl)-3-methyl-2-trifluoromethyl-3H-imidazo[4,5-b]pyridine and 10 ml of chloroform under ice cooling, and then the mixture was stirred at room temperature for 4 hours. A 10% aqueous sodium thiosulfate solution and a saturated aqueous sodium bicarbonate solution were added to the reaction mixture, and the mixture was extracted with ethyl acetate and then dried with anhydrous sodium sulfate. The mixture was concentrated under reduced pressure, and the resulting residue was applied to a silica gel column chromatography to obtain 0.31 g of 6-(2-ethylsulfonylphenyl)-3-methyl-2-trifluoromethyl-3H-imidazo[4,5-b]pyridine (Compound of Present Invention 25).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09328121B1 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-01a5a8cf5b3548e899f4b155dec7d837 |
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| Source note | uspto-grants-2016_05 |
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