HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1473923Generated: October 31, 2026
Sodium Thiosulfate → HCID 86725170, compound
https://huagongshe.com/reaction/1473923
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 86725168 | HCID 86725168 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 86725170 | HCID 86725170 | — |
Reaction Steps
To a mixture of 2-(3-ethylsulfanyl-5-trifluoromethylpyridin-2-yl)-3-methyl-6-trifluoromethyl-3H-imidazo[4,5-b]pyridine (0.61 g) and chloroform (10 ml) was added m-chloroperbenzoic acid (purity: not less than 65%) (0.66 g) while ice-cooling, and the mixture was stirred at room temperature for 10 hours. To the reaction mixture were added aqueous 10% sodium thiosulfate solution and saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with chloroform. The organic layer was washed with water, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to give 2-(3-ethylsulfonyl-5-trifluoromethylpyridin-2-yl)-3-methyl-6-trifluoromethyl-3H-imidazo[4,5-b]pyridine (0.62 g), which is hereinafter referred to as “the present compound 5”.
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-08982c3ae67742e7a8ba57b4fcf7045f |
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| Source note | uspto-grants-2015_04 |
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