HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272907Generated: October 30, 2026
Sodium Thiosulfate → HCID 117974507, compound
https://huagongshe.com/reaction/2272907
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 117974191 | HCID 117974191 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 117974507 | HCID 117974507 | — |
Reaction Steps
0.5 g of 3-chloroperoxybenzoic acid (purity of 65% or more) was added to a mixture of 0.32 g of 2-(2-ethylthiopyrrol-1-yl)-3-methyl-6-trifluoromethyl-3H-imidazo[4,5-b]pyridine and 8 ml of chloroform, under ice cooling, and the mixture was stirred at room temperature for 3 hours and then allowed to stand overnight at room temperature. A 10% aqueous sodium thiosulfate solution was poured to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was washed with a saturated aqueous sodium bicarbonate solution and dried over anhydrous magnesium sulfate, then concentrated under reduced pressure. The resulting residue was applied to a silica gel column chromatography to obtain 0.33 g of 2-(2-ethylsulfonylpyrrol-1-yl)-3-methyl-6-trifluoromethyl-3H-imidazo[4,5-b]pyridine (Compound of Present Invention (24)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09120792B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-2f89a66bffe6492d80c54bd5126eb804 |
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| Source note | uspto-grants-2015_09 |
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