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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1684994Generated: October 29, 2026

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

https://huagongshe.com/reaction/1684994

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 numberUS08148378B2
Source datasetuspto-grants-2012_04
ORD IDord-9f61b40927e548a4bbaafdd1e970d17b
Source noteuspto-grants-2012_04