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Ethyl bromopyruvate → 4-cyclopentyl-5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinoline-1-carboxylic acid ethyl ester

HRID 500453
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 500453
[CH:1]1([CH:6]2[CH2:15][CH2:14][C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[NH:7]2)[CH2:5][CH2:4][CH2:3][CH2:2]1.Br[CH2:17][C:18](=O)[C:19]([O:21][CH2:22][CH3:23])=[O:20].[Cl-].[Mg+2].[Cl-]>O1CCCC1.COCCO>[CH2:22]([O:21][C:19]([C:18]1[C:9]2=[C:8]3[C:13](=[CH:12][CH:11]=[CH:10]2)[CH2:14][CH2:15][CH:6]([CH:1]2[CH2:2][CH2:3][CH2:4][CH2:5]2)[N:7]3[CH:17]=1)=[O:20])[CH3:23]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 66144Ethyl bromopyruvateHCID 5360315Magnesium Chloride2×HCID 650418282-Cyclopentyl-1,2,3,4-tetrahydroquinoline

Produkt 1

HCID 686766484-cyclopentyl-5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinoline-1-carboxylic acid ethyl esterAusbeute 49,5 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 8019
2-Methoxyethanol
Lösungsmittel
2×
HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

To a solution of 2-cyclopentyl-1,2,3,4-tetrahydroquinoline (4.0 g, 20 mmol) in tetrahydrofuran (15 ml) was added ethyl bromopyruvate (˜90% purity; 1.38 ml, 9.9 mmol) and the reaction stirred for 15 h. The resulting precipitate was filtered and washed with tetrahydrofuran (20 ml). The filtrate was evaporated in vacuo. The resulting residue was dissolved in tetrahydrofuran (10 ml) and 2-methoxyethanol (10 ml) and the solution added dropwise to a refluxing solution of magnesium (II) chloride (1.05 g, 11 mmol) in 2-methoxyethanol (10 ml). The reaction mixture was refluxed for 2 h and then a further portion of magnesium (II) chloride (1.05 g, 11 mmol) added and refluxing continued overnight. The reaction was cooled and the solvent removed in vacuo. The resulting brown oil was dissolved in dichloromethane (150 ml) and washed with 2 M HCl (50 ml), saturated potassium carbonate (50 ml) and brine (50 ml). The organics were dried (MgSO4), filtered and the solvent removed in vacuo. The resulting oil was purified by flash chromatography using 33-67% (v/v) dichloromethane in heptane to give 4-cyclopentyl-5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinoline-1-carboxylic acid ethyl ester (1.45 g, 4.9 mmol).

Aufarbeitung

  1. filtrationThe resulting precipitate was filtered
  2. washwashed with tetrahydrofuran (20 ml)
  3. customThe filtrate was evaporated in vacuo
  4. dissolutionThe resulting residue was dissolved in tetrahydrofuran (10 ml)
  5. temperatureThe reaction mixture was refluxed for 2 h
  6. temperaturerefluxing continued overnight
  7. temperatureThe reaction was cooled
  8. customthe solvent removed in vacuo
  9. dissolutionThe resulting brown oil was dissolved in dichloromethane (150 ml)
  10. washwashed with 2 M HCl (50 ml), saturated potassium carbonate (50 ml) and brine (50 ml)
  11. dry with materialThe organics were dried (MgSO4)
  12. filtrationfiltered
  13. customthe solvent removed in vacuo
  14. customThe resulting oil was purified by flash chromatography

Quellen und Nachweise

ORD-Eintrag
ord-88259a6a1ada4cdfb065d3ce7da4ed13
Quelldatensatz
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07772227B2

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