HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1,3-Bis[4-(4-pyridylthio)butyl]-5,5-dimethylhydantoin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-(4-Chlorobutylthio)pyridine | HCID 15816978 | — |
| Reactant | 3-[4-(4-Pyridylthio)butyl]-5,5-dimethylhydantoin | HCID 19079098 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1,3-Bis[4-(4-pyridylthio)butyl]-5,5-dimethylhydantoin | HCID 19079205 | 80.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05246948 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-a61d1f22e885485180fc72a79cdacf3e |
| Source note | uspto-grants-1993_09 |