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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864406Generated: November 1, 2026

Water → HCID 25028839, compound

https://huagongshe.com/reaction/1864406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-Chlorobenzenesulphonyl chlorideHCID 17909—
ReactantSodium hydrideHCID 24758—
Reactant(RS)-5-[4-(2,5-dimethyl-phenyl)-piperazine-1-carbonyl]-1-phenyl-imidazolidin-2-oneHCID 67142096—
SolventDimethylacetamideHCID 31374—
ProductHCID 25028839HCID 25028839—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (RS)-5-[4-(2,5-dimethyl-phenyl)-piperazine-1-carbonyl]-1-phenyl-imidazolidin-2-one (0.050 g) in dimethylacetamide (1 ml) under an argon atmosphere was added sodium hydride (55% in mineral oil, 6.3 mg) at 0° C. The mixture was stirred at 0° C. for 30 min. 3-Chlorobenzenesulfonyl chloride was added. The mixture was stirred at 0° C. for 30 min and at room temperature for 2 h. Water was added and the mixture was extracted with ethyl acetate. The organic phase was washed with water and concentrated. The product was purified by chromatography ((SiO2, cyclohexane=>cyclohexane/ethyl acetate 1:2) to give (RS)-1-(3-chloro-benzenesulfonyl)-4-[4-(2,5-dimethyl-phenyl)-piperazine-1-carbonyl]-3-phenyl-imidazolidin-2-one (0.049 g) as a colorless solid. MS: 552.7 ([M+H]+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625902B2
Source datasetuspto-grants-2009_12
ORD IDord-3fffdbc2c15a4136a42ed34fd755b2ef
Source noteuspto-grants-2009_12