HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1473929Generated: October 30, 2026
Sodium Thiosulfate → HCID 71246869, compound
https://huagongshe.com/reaction/1473929
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 71246825 | HCID 71246825 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 71246869 | HCID 71246869 | 67.9% |
Reaction Steps
To a mixture of 2-(3-ethylsulfonyl-pyridin-2-yl)-3-methyl-6-trifluoromethylsulfanyl-3H-imidazo[4,5-b]pyridine (500 mg) and chloroform (10 ml) was added m-chloroperbenzoic acid (purity: not less than 65%) (429 mg) while ice-cooling, and the mixture was stirred at room temperature for 1 hour and at 50° C. for 2 hours. To the reaction mixture were poured aqueous sodium thiosulfate solution and aqueous sodium hydrogen carbonate solution, and the mixture was extracted with chloroform. The organic layer was dried over sodium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 2-(3-ethylsulfonyl-pyridin-2-yl)-3-methyl-6-trifluoromethylsulfinyl-3H-imidazo[4,5-b]pyridine (353 mg), which is hereinafter referred to as “the present compound 20”.
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-5e270535cabd4cd7861c1560e339d3e9 |
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| Source note | uspto-grants-2015_04 |
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