Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 58878512 | HCID 58878512 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 58878511 | HCID 58878511 | — |
Reaction Steps
4-(2-Bromo-5-methoxy-phenylcarbamoyl)-piperidine-1-carboxylic acid tert-butyl ester (0.5 g, 1.21 mmol) was dissolved in dry N,N-dimethylformamide (5.0 mL). To the reaction mixture was then added at 0° C. sodium hydride (60% in mineral oil, 60.0 mg, 1.45 mmol) under nitrogen atmosphere and the reaction mixture was stirred at 0° C. for one hour. To the reaction mixture was then added at 0° C., ethyl iodide (0.226 g, 1.45 mmol). The reaction mixture was stirred at 0° C. for one hour, then at room temperature under nitrogen atmosphere for 18 hours. The reaction mixture was then added into an excess of water-ice and a solid precipitated. The solid was filtered by suction, washed with water and dried to yield a crude solid. The crude solid was purified via flash chromatography (25% ethyl acetate/hexanes) to yield the title compound as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07655670B2 |
|---|
| Source dataset | uspto-grants-2010_02 |
|---|
| ORD ID | ord-b6b578ee66eb436188e41a10dbccfcc2 |
|---|
| Source note | uspto-grants-2010_02 |
|---|