Dimethylformamide → HCID 58615353, Verbindung

HRID 852998Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 852998
Br[C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[CH:7][CH:6]=[C:5]2[N:12]1[CH2:17][CH2:16][O:15][CH2:14][CH2:13]1.C([Li])CCC.CN(C)[CH:25]=[O:26]>C1COCC1.[Cl-].[NH4+]>[N:12]1([C:5]2[C:4]3[C:9](=[CH:10][CH:11]=[C:2]([CH:25]=[O:26])[CH:3]=3)[N:8]=[CH:7][CH:6]=2)[CH2:17][CH2:16][O:15][CH2:14][CH2:13]1

Komponenten

6

Edukt 3

HCID 6228DimethylformamideHCID 220314084-(6-Bromoquinolin-4-yl)morpholineHCID 178418339Butyllithium

Produkt 1

HCID 58615353HCID 58615353, VerbindungAusbeute 44,5 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 8028TetrahydrofuranLösungsmittel2×HCID 25517Ammonium ChlorideLösungsmittel

Versuchsvorschrift

To a solution of 6-bromo-4-morpholin-4-ylquinoline (1.06 g, 3.62 mmol) in THF (22 mL) was added dropwise a 2.5M solution of n-butyllithium in hexanes (1.74 mL, 4.34 mmol, 1.2 equiv.) at −70° C. During the addition, the color of the solution was turned into red and this solution was stirred for 1 h at this temperature. Then, a solution of dimethylformamide (0.558 mL, 7.23 mmol) in THF (2 mL) was added dropwise. After addition, the mixture was allowed to warm to room temperature and stirred for 2 h. Then, the mixture was diluted with saturated ammonium chloride solution and the two layers were separated. The aqueous layer was extracted with ethyl acetate (3×50 mL). The combined organic extracts were washed with brine solution and dried over anhydrous magnesium sulfate. Filtration of the drying agent and removal of the solvent under the vacuum gave the crude residue which was purified by using a Biotage silica gel column chromatography to afford 0.390 g (44.5% yield) of 4-morpholin-4-yl-quinoline-6-carbaldehyde as a white solid: EI-LRMS m/e calcd for C14H14N2O2 (M+) 243.1, found 243.1.

Aufarbeitung

  1. additionDuring the addition
  2. additionAfter addition
  3. stirringstirred for 2 h
  4. customthe two layers were separated
  5. extractionThe aqueous layer was extracted with ethyl acetate (3×50 mL)
  6. washThe combined organic extracts were washed with brine solution
  7. dry with materialdried over anhydrous magnesium sulfate
  8. filtrationFiltration of the drying agent and removal of the solvent under the vacuum
  9. customgave the crude residue which
  10. customwas purified

Quellen und Nachweise

ORD-Eintrag
ord-9e64c4704af84ef4a5ae92a26b1bad02
Quelldatensatz
uspto-grants-2007_08
Patentnummer
US07253285B2

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