Ethanol → 3-(3-Hexyl-6-isopropyl-3-azabicyclo[3.1.0]hex-6-yl)aniline

HRID 1826451Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1826451
[CH2:1]([N:7]1[CH2:12][CH:11]2[CH:9]([C:10]2([CH:22]([CH3:24])[CH3:23])[C:13]2[CH:18]=[CH:17][CH:16]=[C:15]([N+:19]([O-])=O)[CH:14]=2)[CH2:8]1)[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6].C(O)C.[Cl-].[Ca+2].[Cl-]>O.[Fe]>[CH2:1]([N:7]1[CH2:12][CH:11]2[CH:9]([C:10]2([C:13]2[CH:14]=[C:15]([CH:16]=[CH:17][CH:18]=2)[NH2:19])[CH:22]([CH3:24])[CH3:23])[CH2:8]1)[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6]

Komponenten

6

Versuchsvorschrift

To a stirred suspension of 3-hexyl-6-isopropyl-6-(3-nitrophenyl)-3-azabicyclo[3.1.0]hexane (Preparation 60, 0.18 g, 0.54 mmol), ethanol (15 ml) and iron powder (0.27 g, 4.88 mmol) was added calcium chloride (0.06 gm 0.54 mmol) in water (3 ml). The reaction mixture was heated under reflux for 3 h and then filtered through a pad of Celite®, the mother liquors were concentrated in vacuo. The residue was dissolved in dichloromethane and filtered again through a Sep-Pak® Plus cartridge containing silica (1.5 g), (Water Division Millipore), to remove any residual iron salts and then concentrated to give the crude title compound as a yellow solid (0.17 g, 100%).

Aufarbeitung

  1. temperatureThe reaction mixture was heated
  2. temperatureunder reflux for 3 h
  3. filtrationfiltered through a pad of Celite®
  4. concentrationthe mother liquors were concentrated in vacuo
  5. dissolutionThe residue was dissolved in dichloromethane
  6. filtrationfiltered again through a Sep-Pak® Plus cartridge
  7. additioncontaining silica (1.5 g), (Water Division Millipore),
  8. customto remove any residual iron salts
  9. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-3ef871c7b0b9423d8691b73add77e472
Quelldatensatz
uspto-grants-2006_05
Patentnummer
US07049444B2

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