Phosphorus tribromide → (+/-)-trans-2-Bromo-6-propyl-5,5a,6,7,8,9,9a,10-octahydropyrido[2,3-g]quinoline dihydrobromide

HRID 1110704Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1110704
P(Br)(Br)[Br:2].O=[C:6]1[NH:22][C:10]2[CH2:11][C@H:12]3[C@H:17]([CH2:18][C:9]=2[CH:8]=[CH:7]1)[N:16]([CH2:19][CH2:20][CH3:21])[CH2:15][CH2:14][CH2:13]3>CN(C)C=O>[BrH:2].[BrH:2].[Br:2][C:6]1[CH:7]=[CH:8][C:9]2[CH2:18][C@H:17]3[C@@H:12]([CH2:13][CH2:14][CH2:15][N:16]3[CH2:19][CH2:20][CH3:21])[CH2:11][C:10]=2[N:22]=1

Komponenten

4

Versuchsvorschrift

Phosphorus tribromide (30.7 mL, 87.5 g, 324 mMol) was added dropwise over 22 hours to a solution of (±)-trans-2-oxo-6-propyl-1,2,5,5a,6,7,8,9,9a,10-decahydropyrido[2,3-g]quinoline (1.50 g, 6.06 mMol) in dimethylformamide (100 mL) at 100° C. The reaction was quenched by the dropwise addition of water (50 mL). This mixture was poured over ice and made basic by addition of NH4OH and extracted with methylene chloride. The extract was dried (Na2SO4) and concentrated to give a brown oil. Purification by flash chromatography (7% methanol in methylene chloride, 0.5% NH4OH) gave the desired product as an orange oil (Rf =0.54, 1.22 g, 65% yield).

Aufarbeitung

  1. customThe reaction was quenched by the dropwise addition of water (50 mL)
  2. additionThis mixture was poured over ice
  3. additionmade basic by addition of NH4OH
  4. extractionextracted with methylene chloride
  5. dry with materialThe extract was dried (Na2SO4)
  6. concentrationconcentrated
  7. customto give a brown oil
  8. customPurification by flash chromatography (7% methanol in methylene chloride, 0.5% NH4OH)

Quellen und Nachweise

ORD-Eintrag
ord-1b0a53bb39be4be188fc1a09ca291899
Quelldatensatz
uspto-grants-1990_12
Patentnummer
US04977149

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