HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552864Generated: October 30, 2026
Sodium Dithionite → HCID 178466115, compound
https://huagongshe.com/reaction/552864
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Hydrogen chloride-ethyl acetate | HCID 21866389 | — |
| Reactant | HCID 178503671 | HCID 178503671 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178466115 | HCID 178466115 | — |
Reaction Steps
To a solution of 2-[2-(methylthio)ethyl]-5-{5-[3-(trifluoromethyl)-4-(2,2,2-trifluoro-1-methylethoxy)phenyl]-1,2,4-oxadiazol-3-yl}-1H-benzimidazole (400 mg) in dichloromethane (8.0 ml) was added mCPBA (534 mg), followed by stirring at room temperature for 3 hours. To the reaction mixture was added a Na2S2O4 aqueous solution, followed by stirring for 1 hour. The reaction solution was extracted three times with EtOAc, and the organic layer was combined, dried over anhydrous MgSO4, filtered, and then concentrated. The residue was purified by silica gel chromatography (chloroform:CH3OH=10:1) to obtain a yellow oily substance. This was dissolved in EtOAc, and a 4M-HCl/EtOAc solution was added thereto, followed by concentration. The residue was washed with IPE to obtain 2-[2-(methylsulfonyl)ethyl]-5-{5-[3-(trifluoromethyl)-4-(2,2,2-trifluoro-1-methylethoxy)phenyl]-1,2,4-oxadiazol-3-yl}-1H-benzimidazole hydrochloride (146 mg) as pale yellow powders.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07951825B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-4e6956af8a4d4b8ca07698a475644bfa |
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| Source note | uspto-grants-2011_05 |
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