HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → HCID 59631366, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 59631383 | HCID 59631383 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59631366 | HCID 59631366 | — |
Reaction Steps
The 4-(4-bromo-5,7-difluoro-3-methylquinolin-2-yl)piperazin-2-one (70 mg, 0.20 mmol) was dissolved in THF (2.0 mL). To the solution was added sodium hydride (24.0 mg, 1.00 mmol) (60% dispersion) followed by addition of ethyl iodide (0.16 mL, 2.00 mmol). The reaction was stirred overnight. The reaction was quenched with water and the mixture was extracted with EtOAc (2×50 mL). The combined organic layers were washed with brine (1×25 mL) and dried over magnesium sulfate. The crude product was purified by medium pressure chromatography (silica gel, 0 to 100% EtOAc:hexanes) to give 4-(4-bromo-5,7-difluoro-3-methylquinolin-2-yl)-1-ethylpiperazin-2-one. Mass Spectrum (ESI) m/e=384.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08940724B2 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-fcdc618ba7554c7b84553ffdde040e7b |
| Source note | uspto-grants-2015_01 |