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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552864Generated: October 30, 2026

Sodium Dithionite → HCID 178466115, compound

https://huagongshe.com/reaction/552864

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium DithioniteHCID 24489—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHydrogen chloride-ethyl acetateHCID 21866389—
ReactantHCID 178503671HCID 178503671—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 178466115HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951825B2
Source datasetuspto-grants-2011_05
ORD IDord-4e6956af8a4d4b8ca07698a475644bfa
Source noteuspto-grants-2011_05