HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272894Generated: November 1, 2026
Sodium Thiosulfate → HCID 117974275, compound
https://huagongshe.com/reaction/2272894
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 117974290 | HCID 117974290 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 117974275 | HCID 117974275 | — |
Reaction Steps
0.22 g of 3-chloroperoxybenzoic acid (purity of 65% or more) was added to 3 ml of a solution of 0.13 g of 2-(2-ethylthio-3H-imidazol-3-yl)-3-methyl-6-trifluoromethyl-3H-imidazo[4,5,b]pyridine in chloroform under ice cooling, and the mixture was stirred at room temperature for 1 hour. A 10% aqueous sodium thiosulfate solution was poured into the reaction mixture, and the mixture was extracted with chloroform. The organic layer was washed with a saturated aqueous sodium bicarbonate solution, then dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting residue was applied to a silica gel column chromatography to obtain 0.12 g of 2-(2-ethylsulfonyl-3H-imidazol-3-yl)-3-methyl-6-trifluoromethyl-3H-imidazo[4,5,b]pyridine (Compound of Present Invention (2)).
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-359bab8262544379b3a4bb093ade1acb |
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| Source note | uspto-grants-2015_09 |
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