HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1473933Generated: October 30, 2026
Sodium Thiosulfate → HCID 86725175, compound
https://huagongshe.com/reaction/1473933
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 86725176 | HCID 86725176 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 86725175 | HCID 86725175 | — |
Reaction Steps
To a mixture of 2-(3-ethylsulfanyl-5-trifluoromethyl-pyridin-2-yl)-3-methyl-6-trifluoromethylsulfanyl-3H-imidazo[4,5-b]pyridine (299 mg) and chloroform (30 ml) was added m-chloroperbenzoic acid (purity: not less than 65%) (0.34 g) while ice-cooling, and the mixture was stirred while ice-cooling for 5 hours. To the reaction mixture were poured saturated aqueous sodium hydrogen carbonate solution and saturated aqueous sodium thiosulfate solution, and the mixture was extracted with chloroform. The organic layer was dried over magnesium sulfate and concentrated under reduced pressure. The resulting residue was subjected to silica gel column chromatography to give 2-(3-ethylsulfonyl-5-trifluoromethyl-pyridin-2-yl)-3-methyl-6-trifluoromethylsulfanyl-3H-imidazo[4,5-b]pyridine (0.24 g), which is hereinafter referred to as “the present compound 44”.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09018134B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-1430070573964109a0d70f8bbda8d5d8 |
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| Source note | uspto-grants-2015_04 |
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