Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 4-Nitrobenzoyl chloride | HCID 8502 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Reactant | HCID 53965189 | HCID 53965189 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 54189901 | HCID 54189901 | 94.2% |
Reaction Steps
(S)-(+)-4-phenyl-1-(indoline-5-sulfonyl)-4,5-dihydro-2-imidazolone (0.72 g, 2.09 mmol) prepared in Preparation 8 was dissolved in 20 m of dichloromethane. Then, pyridine (186 μ, 2.23 mmol) and 4-nitrobenzoyl chloride (413 mg, 2.23 mmol) were added thereto at 0° C. under nitrogen atmosphere one after another. The reaction mixture was stirred at 5° C. for 2 hours and further stirred at room temperature for 3 hours. Then, the reaction mixture was diluted with 20 m of dichloromethane, washed with water, dried over anhydrous magnesium sulfate, concentrated and finally purified by silica gel column chromatography (eluent: ethylacetate/hexane=2/1, v/v) to afford 0.97 g (Yield: 93%) of (S)-(+)-4-phenyl-l-[N-(4-nitrobenzoyl)-indoline-5 -sulfonyl]-4,5-dihydro-2-imidazolone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05929103 |
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| Source dataset | uspto-grants-1999_07 |
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| ORD ID | ord-c97be6fc6b9546d49d08e89f4f4c8629 |
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| Source note | uspto-grants-1999_07 |
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