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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 964158Generated: October 30, 2026

Water → 1,3-Bis[4-(4-pyridylthio)butyl]-5,5-dimethylhydantoin

https://huagongshe.com/reaction/964158

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant4-(4-Chlorobutylthio)pyridineHCID 15816978—
Reactant3-[4-(4-Pyridylthio)butyl]-5,5-dimethylhydantoinHCID 19079098—
SolventDimethylformamideHCID 6228—
Product1,3-Bis[4-(4-pyridylthio)butyl]-5,5-dimethylhydantoinHCID 1907920580.7%

Reaction Steps

To a suspension of 96 mg (2.4 mmol) of 60% sodium hydride (oily) in 15 ml of dimethylformamide, 587 mg (2.0 mmol) of 3-[4-(4-pyridylthio)butyl]-5,5-dimethylhydantoin was added, and the mixture was stirred at room temperature for 10 minutes. To this reaction mixture, 807 mg (4.0 mmol) of 4-(4-chlorobutylthio)pyridine was added with stirring under ice-cooling, and the mixture was stirred at 80° C. for 16 hours. After cooling, water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was dried and the solvent was distilled off. The residue was purified by column chromatography (eluent: ethyl acetate/ethanol=10:1) to give 0.74 g of the desired product (80.7% yield, yellow oil).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05767121
Source datasetuspto-grants-1998_06
ORD IDord-4ad1c0925bc54ccdb15eb6e24beeef4f
Source noteuspto-grants-1998_06