Reaktion #658268
ord-d00e67e6c0064cadbaed9e1c1d69663e
Reaktionsgleichung
Edukte
Reagenzien
Reaktionsbedingungen
Aufarbeitung
- 1workup.ADDITIONwas added
- 2Temperaturthe reaction mixture was heated
- 3Temperaturat reflux under N2 for 16 hr
- 4Sonstigewas partitioned between EtOAc (100 mL) and water (150 mL)
- 5SonstigeThe organic layer was separated
- 6Waschenwas washed with aq. citric acid solution (10% w/v, 50 mL)
- 7Sonstigedried
- 8Sonstigeevaporated in vacuo
- 9SonstigeThe residue was purified by flash column chromatography (SiO2, 80 g, EtOAc in isohexane, 0-70%, gradient elution)
- 10SonstigeThe impure product so obtained
- 11Filtrationthe resulting precipitate was collected by filtration
Vorschrift
To a solution of 4-iodo-1,2-dimethoxybenzene (1.10 g, 4.17 mmol) in anhydrous toluene (5.0 mL) was added 3-tert-butyl-1H-pyrazol-5-amine (638 mg, 4.58 mmol) followed by (1R,2R)—N1,N2-dimethylcyclohexane-1,2-diamine (130 μL, 0.83 mmol) and potassium carbonate (1.15 g, 8.3 mmol). The mixture was purged with N2, copper(I) iodide (40 mg, 0.21 mmol) was added and the reaction mixture was heated at reflux under N2 for 16 hr. The resulting mixture was cooled to RT and was partitioned between EtOAc (100 mL) and water (150 mL). The organic layer was separated and was washed with aq. citric acid solution (10% w/v, 50 mL) followed by brine (50 mL) and then dried and evaporated in vacuo. The residue was purified by flash column chromatography (SiO2, 80 g, EtOAc in isohexane, 0-70%, gradient elution). The impure product so obtained was dissolved in ether (1.0 mL), isohexane (10 mL) was added and the resulting precipitate was collected by filtration to afford the title compound, Intermediate A19, as a purple solid (364 mg, 31%); Rt 3.55 min (Method 1); m/z 276 (M+H)+ (ES+).