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Lithium Carbonate → HCID 18671697, Verbindung

HRID 1057610
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1057610
C1C=C[NH+]=CC=1.Br[Br-]Br.[CH2:10]([N:17]1[C:29]2[CH2:28][CH2:27][CH2:26][C:25](=[O:30])[C:24]=2[C:23]2[C:18]1=[C:19]([F:31])[CH:20]=[CH:21][CH:22]=2)[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.[Br-].[Li+].C(=O)([O-])[O-].[Li+].[Li+]>C1COCC1.CN(C=O)C>[CH2:10]([N:17]1[C:29]2[CH:28]=[CH:27][CH:26]=[C:25]([OH:30])[C:24]=2[C:23]2[C:18]1=[C:19]([F:31])[CH:20]=[CH:21][CH:22]=2)[C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 11125Lithium CarbonateHCID 82050Lithium BromideHCID 18671682HCID 18671682, Verbindung

Produkt 1

HCID 18671697HCID 18671697, VerbindungAusbeute 52 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6228DimethylformamideLösungsmittel2×
HCID 8028
Tetrahydrofuran
Lösungsmittel

Reaktionsbedingungen

Temperatur
75 °C

Versuchsvorschrift

Pyridinium bromide perbromide (2.9945 g, 0.0094 mol) is added to a mixture of 9-benzyl-8-fluoro-1,2,3,9-tetrahydro-4H-carbazol-4-one (2.1145 g, 0.0072 mol) in THF (22 mL) and DMF (16 mL) and the mixture is heated to 75° C. After stirring for 5.5 h, THF is removed under reduced pressure and the residue is partitioned between ethyl acetate and brine. The combined organic layers are washed with dilute sodium thiosulfate/brine and the aqueous layer is backwashed with ethyl acetate. The combined organic layers are dried over magnesium sulfate and concentrated under reduced pressure to give a residue. The residue is recrystallized from ethyl acetate/heptane and the resulting solids are combined with lithium bromide (1.1338 g, 0.013 mol), lithium carbonate (0.8831 g, 0.012 mol), and DMF (24 mL) and heated to 120° C. After 1.5 h, the mixture is partitioned between ethyl acetate and brine. The combined organic layers are washed with dilute brine and then dried over sodium sulfate and concentrated to an oil. The oil is chromatographed on silica gel (150 mL) using dichloromethane (100) to give 1.0857 g (52%) of the title compound; mp 155-156° C.; MS (ESI−) for C19H14FNO m/z 290.1 (M−H)−; IR (drift) 3524, 1581, 1498, 1456, 1432, 1343, 1318, 1272, 1239, 1134, 966, 790, 731, 714, 698 cm−1; 1H NMR (CDCl3) δ5.33, 5.69, 6.59, 6.98, 7.14, 7.25, 8.10. Anal. Calcd for C19H14FNO: C, 78.33; H, 4.84; N, 4.81. Found: C, 77.67; H, 4.90; N, 4.71.

Aufarbeitung

  1. customTHF is removed under reduced pressure
  2. customthe residue is partitioned between ethyl acetate and brine
  3. washThe combined organic layers are washed with dilute sodium thiosulfate/brine
  4. dry with materialThe combined organic layers are dried over magnesium sulfate
  5. concentrationconcentrated under reduced pressure
  6. customto give a residue
  7. customThe residue is recrystallized from ethyl acetate/heptane
  8. temperatureheated to 120° C
  9. waitAfter 1.5 h
  10. customthe mixture is partitioned between ethyl acetate and brine
  11. washThe combined organic layers are washed with dilute brine
  12. dry with materialdried over sodium sulfate
  13. concentrationconcentrated to an oil
  14. customThe oil is chromatographed on silica gel (150 mL)

Quellen und Nachweise

ORD-Eintrag
ord-a15abd2a5823416d86650ea97084f1f3
Quelldatensatz
uspto-grants-2003_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06514968B1

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