HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530906Generated: October 30, 2026
Sodium Thiosulfate → HCID 86725173, compound
https://huagongshe.com/reaction/530906
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 86725171 | HCID 86725171 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 86725173 | HCID 86725173 | 3% |
Reaction Steps
To a mixture of 2-(3-ethylsulfanyl-pyridin-2-yl)-3-methyl-6-pentafluoroethyl-3H-imidazo[4,5-b]pyridine (254 mg) and chloroform (10 ml) was added m-chloroperbenzoic acid (purity: not less than 65%) (266 mg) while ice-cooling. The mixture was heated to room temperature and then stirred for 0.5 hours. To the mixture were poured saturated aqueous sodium hydrogen carbonate solution and saturated aqueous sodium thiosulfate solution, and the mixture was extracted with chloroform. The organic layer was dried over magnesium sulfate and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 2-(3-ethane sulfinyl-pyridin-2-yl)-3-methyl-6-pentafluoroethyl-3H-imidazo[4,5-b]pyridine (8 mg), which is hereinafter referred to as “the present compound 7”), and 2-(3-ethanesulfonyl-pyridin-2-yl)-3-methyl-6-pentafluoroethyl-3H-imidazo[4,5-b]pyridine (235 mg), which is hereinafter referred to as “the present compound 8”.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09353110B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-e2e7bf2c3917451da9532cb3ab19874b |
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| Source note | uspto-grants-2016_05 |
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