Potassium Carbonate → HCID 15745003, Verbindung

HRID 1648285Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1648285
[CH2:1]([NH:4][CH:5]1[CH2:14][C:13]2=[CH:15][CH:16]=[CH:17][C:11]3=[C:12]2[N:7]([CH2:8][CH2:9][CH2:10]3)[CH2:6]1)[CH2:2][CH3:3].[CH2:18](I)[CH2:19][CH3:20].C(=O)([O-])[O-].[K+].[K+].[OH-].[Na+]>CN(C)C=O.C(OCC)(=O)C>[CH2:1]([N:4]([CH2:18][CH2:19][CH3:20])[CH:5]1[CH2:14][C:13]2=[CH:15][CH:16]=[CH:17][C:11]3=[C:12]2[N:7]([CH2:8][CH2:9][CH2:10]3)[CH2:6]1)[CH2:2][CH3:3]

Komponenten

7

Reaktionsbedingungen

Temperatur
90 °C

Versuchsvorschrift

A mixture of 2,3,6,7-tetrahydro-N-propyl-1H,5H-benzo(ij)quinolizin-2-amine (2.33 g, 0.01 tool), propyl iodide (5.16 g, 0.03 tool) and anhydrous potassium carbonate (3 g, 0.02 tool) in dimethylformamide (75 mL) was stirred for 5 hours at 90° C. At this time additional propyl iodide (1.72 g, 0.01 mol) and potassium carbonate (0.5 g, 0.0036 mol) were added and the reaction was continued for an additional 2 hours. The reaction was cooled, filtered to remove inorganic material, and the solvent was removed under reduced pressure. The product was partitioned between ethyl acetate (800 mL) and 4N sodium hydroxide (20 mL, 0.08 mol), the organic layer concentrated, filtered, and chromatographed on silica gel in 5-30% ethyl acetate:hexane to give 2.19 g of 2,3,6,7-tetrahydro-N,N-dipropyl-1H,5H-benzo(ij)quinolizin-2-amine.

Aufarbeitung

  1. waitthe reaction was continued for an additional 2 hours
  2. temperatureThe reaction was cooled
  3. filtrationfiltered
  4. customto remove inorganic material
  5. customthe solvent was removed under reduced pressure
  6. concentrationthe organic layer concentrated
  7. filtrationfiltered
  8. customchromatographed on silica gel in 5-30% ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-591497503df14e2286c02fe00b8b16d7
Quelldatensatz
uspto-grants-1995_07
Patentnummer
US05436240

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