Реакция #43997

ord-75b8ec8489e648b0ae41eabd693a6b21

Уравнение реакции

O=S([O-])S(=O)(=O)[O-].[Na+].[Na+]
Sodium metabisulphite
Nc1ccc(CC(=O)O)cc1
4-aminophenyl acetic acid
CCN(CC)CC
triethylamine
CCOC(=O)c1c(C)c(OC)c2ccccc2c1OC
ethyl 1,4-dimethoxy-2-methylnaphthalene-3-carboxylate
O=C1CCC(=O)N1Br
N-bromosuccinimide
c1ccc(COOCc2ccccc2)cc1
dibenzylperoxide
COc1c2c(c(OC)c3ccccc13)C(=O)N(c1ccc(CC(=O)O)cc1)C2
[4-(4,9-dimethoxy-1-oxo-1,3-dihydro-2H-benzo[f]isoindol-2-yl)phenyl]acetic acid
Выход 15.0%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ТемператураThe mixture was heated
  2. 2
    Температураat reflux under nitrogen for 45 min
  3. 3
    Другоеilluminating with a 200 W lamp
  4. 4
    Температураthe mixture refluxed for 3 h under nitrogen
  5. 5
    Другоеthe reaction evaporated to dryness under vacuum
  6. 6
    ДругоеThe product was partially purified by SPE (NH2, 10 g)
  7. 7
    Промывкаeluting with methanol
  8. 8
    workup.ADDITIONThe fractions containing product
  9. 9
    Промывкаwashing with 5% acetic acid in methanol
  10. 10
    ДругоеAfter evaporation of the solvents under vacuum
  11. 11
    Промывкаeluting 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%).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07732622B2uspto-grants-2010_06