HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256599Generated: October 31, 2026
Sodium Thiosulfate → HCID 66612071, compound
https://huagongshe.com/reaction/1256599
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 66611813 | HCID 66611813 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 66612071 | HCID 66612071 | — |
Reaction Steps
To a mixture of 0.60 g of 1-methyl-2-(3-methylthiopyridin-4-yl)-5-trifluoromethyl-1H-benzimidazole and 9 ml of chloroform was added 1.40 g of 69% m-chloroperbenzoic acid under ice cool, then, the mixture was stirred for 2 hours at room temperature. Thereafter, a saturated sodium hydrogen carbonate aqueous solution and a saturated sodium thiosulfate aqueous solution were poured, and the mixture was extracted three times with chloroform. The combined organic layers were dried over magnesium sulfate, then, concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 0.52 g of 2-(3-methanesulfonylpyridin-4-yl)-1-methyl-5-trifluoromethyl-1H-benzimidazole (hereinafter, referred to as present active compound 19).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08461181B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-4b80650378794d3b8778edee4d120548 |
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| Source note | uspto-grants-2013_06 |
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