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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108370Generated: October 30, 2026

Methanol → {4-[6-(2-Phenylethanesulfinyl)pyridazin-3-YL]piperazin-1-YL}-(2-trifluoromethylphenyl)methanone

https://huagongshe.com/reaction/2108370

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant[4-(6-Phenethylsulfanylpyridazin-3-YL)piperazin-1-YL](2-trifluoromethylphenyl)methanoneHCID 11155686—
ReactantSodium periodateHCID 23667635—
SolventWaterHCID 962—
Product{4-[6-(2-Phenylethanesulfinyl)pyridazin-3-YL]piperazin-1-YL}-(2-trifluoromethylphenyl)methanoneHCID 1117929469.2%

Reaction Steps

To an ice-cold solution of sodium periodate (0.025 g, 0.12 mmol) in 1:1 mixture of water and methanol was added [4-(6-phenethylsulfanylpyridazin-3-yl)piperazin-1-yl]-(2-trifluoromethylphenyl)methanone. The reaction mixture was stirred at room temperature over night, diluted with water and then extracted with dichloromethane. The organic layer was washed with water, dried over anhydrous MgSO4 and then concentrated in vacuo. The residue was purified by column chromatography to yield the title compound as a white solid (41 mg, 69.2%). 1H NMR (400 MHz, CDCl3) δ 7.86, 7.75, 7.63-7.66, 7.56-7.59, 7.37, 7.25-7.28, 7.21-7.17, 7.07-7.09, 4.04-4.10, 3.83-3.91, 3.70-3.80, 3.45-3.35, 3.26-3.30, 3.2-3.15.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514436B2
Source datasetuspto-grants-2009_04
ORD IDord-501fbef82eed46088ea185458f802c95
Source noteuspto-grants-2009_04