Реакция #43997
ord-75b8ec8489e648b0ae41eabd693a6b21
Уравнение реакции
Реактанты
Реагенты
Растворители
Условия реакции
Обработка
- 1ТемператураThe mixture was heated
- 2Температураat reflux under nitrogen for 45 min
- 3Другоеilluminating with a 200 W lamp
- 4Температураthe mixture refluxed for 3 h under nitrogen
- 5Другоеthe reaction evaporated to dryness under vacuum
- 6ДругоеThe product was partially purified by SPE (NH2, 10 g)
- 7Промывкаeluting with methanol
- 8workup.ADDITIONThe fractions containing product
- 9Промывкаwashing with 5% acetic acid in methanol
- 10ДругоеAfter evaporation of the solvents under vacuum
- 11Промывкаeluting with a gradient (1:1 ethyl acetate/cyclohexane to 5% methanol, 1% acetic acid in 1:1 ethyl acetate/cyclohexane)
Методика
To a solution of ethyl 1,4-dimethoxy-2-methylnaphthalene-3-carboxylate (73 mg, 0.266 mmol) in carbon tetrachloride (10 ml) was added N-bromosuccinimide (47 mg, 0.266 mmol) and dibenzylperoxide (5 mg). The mixture was heated at reflux under nitrogen for 45 min, illuminating with a 200 W lamp. The reaction was cooled to room temperature, 4-aminophenyl acetic acid (40 mg, 0.266 mmol), triethylamine (74 μl, 0.53 mmol) and DMF (5 ml) added and the reaction stirred for 48 h. Acetic acid (glacial, 1 ml) was added to the reaction and the mixture refluxed for 3 h under nitrogen. Sodium metabisulphite solution (1 ml) was added and the reaction evaporated to dryness under vacuum. The product was partially purified by SPE (NH2, 10 g) eluting with methanol then 5% acetic acid in methanol. The fractions containing product were passed through a silica plug washing with 5% acetic acid in methanol. After evaporation of the solvents under vacuum, the residue was columned on a silica gel flash column eluting with a gradient (1:1 ethyl acetate/cyclohexane to 5% methanol, 1% acetic acid in 1:1 ethyl acetate/cyclohexane) to give [4-(4,9-dimethoxy-1-oxo-1,3-dihydro-2H-benzo[f]isoindol-2-yl)phenyl]acetic acid (15 mg, 15%).