HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 4-phenyl-1-(N-chloroacetyl-2-methylindoline-5-sulfonyl)-2-imidazolone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | HCID 21224941 | HCID 21224941 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-phenyl-1-(N-chloroacetyl-2-methylindoline-5-sulfonyl)-2-imidazolone | HCID 21224872 | 94% |
Reaction Steps
4-Phenyl-1-(2-methylindoline-5-sulfonyl)-2-imidazolone (300 mg, 0.85 mmol) prepared in Preparation 3 was dissolved in 10 m of dichloromethane. Pyridine (75 μ, 0.93 mmol) and chloroacetylchloride (74 μ, 0.93 mmol) were added thereto one after another, and then the reaction mixture was stirred at room temperature under nitrogen atmosphere for 2 hours. After stirring, the reaction mixture was diluted with 50 m of dichloromethane, washed with water, dried over anhydrous magnesium sulfate, and then concentrated. The residue was purified by silica gel column chromatography (eluent:dichloromethane/methanol=10/1, v/v) to afford 342 mg of the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05929103 |
| Source dataset | uspto-grants-1999_07 |
| ORD ID | ord-1c1248fd31b9462a8283dcef0b96fc2a |
| Source note | uspto-grants-1999_07 |