Triethylamine → [4-(4,9-dimethoxy-1-oxo-1,3-dihydro-2H-benzo[f]isoindol-2-yl)phenyl]acetic acid

HRID 1375140

반응식

HRID 1375140 반응식
[CH3:1][O:2][C:3]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[C:6]([O:13][CH3:14])=[C:5]([C:15]([O:17]CC)=O)[C:4]=1[CH3:20].BrN1C(=O)CCC1=O.C(OOCC1C=CC=CC=1)C1C=CC=CC=1.[NH2:45][C:46]1[CH:51]=[CH:50][C:49]([CH2:52][C:53]([OH:55])=[O:54])=[CH:48][CH:47]=1.C(N(CC)CC)C.S(S([O-])=O)([O-])(=O)=O.[Na+].[Na+]>C(Cl)(Cl)(Cl)Cl.C(O)(=O)C.CN(C=O)C>[CH3:1][O:2][C:3]1[C:4]2[CH2:20][N:45]([C:46]3[CH:47]=[CH:48][C:49]([CH2:52][C:53]([OH:55])=[O:54])=[CH:50][CH:51]=3)[C:15](=[O:17])[C:5]=2[C:6]([O:13][CH3:14])=[C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][C:12]=12

참가 물질

10

반응물 6

HCID 8471TriethylamineHCID 145334-Aminophenylacetic acidHCID 67184N-bromobutanimideHCID 656671Sodium PyrosulfiteHCID 11229634Benzyl PeroxideHCID 11369352Ethyl 1,4-dimethoxy-3-methyl-2-naphthoate

생성물 1

HCID 9864500[4-(4,9-dimethoxy-1-oxo-1,3-dihydro-2H-benzo[f]isoindol-2-yl)phenyl]acetic acid수율 15%

시약·촉매·용매 3

HCID 176Acetic Acid용매HCID 5943Carbon Tetrachloride용매HCID 6228Dimethylformamide용매

실험 절차

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%).

후처리

  1. temperatureThe mixture was heated
  2. temperatureat reflux under nitrogen for 45 min
  3. customilluminating with a 200 W lamp
  4. temperaturethe mixture refluxed for 3 h under nitrogen
  5. customthe reaction evaporated to dryness under vacuum
  6. customThe product was partially purified by SPE (NH2, 10 g)
  7. washeluting with methanol
  8. additionThe fractions containing product
  9. washwashing with 5% acetic acid in methanol
  10. customAfter evaporation of the solvents under vacuum
  11. washeluting with a gradient (1:1 ethyl acetate/cyclohexane to 5% methanol, 1% acetic acid in 1:1 ethyl acetate/cyclohexane)

출처 및 근거

ORD 기록
ord-9e96867c226b40268b16bb68b689190b
출처 데이터셋
uspto-grants-2007_01
특허 번호
US07166631B2

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