HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 918787Generated: October 31, 2026
Sodium Thiosulfate → HCID 72703862, compound
https://huagongshe.com/reaction/918787
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 72703864 | HCID 72703864 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 72703862 | HCID 72703862 | — |
Reaction Steps
436 mg of 3-chloroperoxybenzoic acid (purity of 65% or more) was added to a mixture of 236 mg of 2-(2-ethylsulfanyl-4-trifluoromethylphenyl)-6-trifluoromethyl-imidazo[1,2-a]pyridine and 5 ml of chloroform under ice cooling, and the mixture was stirred at room temperature for 4 hours. 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 122 mg of 2-(2-ethylsulfonyl-4-trifluoromethylphenyl)-6-trifluoromethyl-imidazo[1,2-a]pyridine (hereinafter, referred to as Compound of Present Invention 7).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09271500B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-17f073b2feae43b1b261f41d1a66eacb |
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| Source note | uspto-grants-2016_03 |
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