Sodium Hydroxide → 1-butyl-4,4-bis(5-fluoro-3-methyl-1H-indol-2-yl)-N,N-dimethylcyclohexanamine

HRID 1011623Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1011623
[F:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][CH:6]=[C:5]2[CH3:11].[CH2:12]([C:16]1([N:23]([CH3:25])[CH3:24])[CH2:21][CH2:20][C:19](=O)[CH2:18][CH2:17]1)[CH2:13][CH2:14][CH3:15].F[C:27]([F:33])(F)S(O)(=O)=O.[OH-].[Na+]>ClCCl>[CH2:12]([C:16]1([N:23]([CH3:25])[CH3:24])[CH2:21][CH2:20][C:19]([C:6]2[NH:7][C:8]3[C:4]([C:5]=2[CH3:11])=[CH:3][C:27]([F:33])=[CH:10][CH:9]=3)([C:6]2[NH:7][C:8]3[C:4]([C:5]=2[CH3:11])=[CH:3][C:2]([F:1])=[CH:10][CH:9]=3)[CH2:18][CH2:17]1)[CH2:13][CH2:14][CH3:15]

Komponenten

6

Versuchsvorschrift

5-fluoro-3-methyl indole (596 mg, 4 mmol) together with 4-butyl-4-(dimethylamino)-cyclohexanone (788 mg, 4 mmol, synthesis cf. WO2008009415, ketone unit Ket-4) was dissolved in dichloromethane (30 ml) and mixed with trifluoromethane sulphonic acid (400 μl, 4.6 mmol). The batch was stirred for 24 h at RT. For work up the reaction mixture was mixed with 2N NaOH (30 ml) and stirred for 20 min at RT. After separation of the organic phase the aqueous phase was extracted with dichloromethane (3×15 ml). The combined organic extracts were dried over Na2SO4 and then concentrated to low volume. The raw product obtained (1.4 g) was purified by column chromatography [silica gel 60 (50 g); ethyl acetate (500 ml)].

Aufarbeitung

  1. stirringstirred for 20 min at RT
  2. customAfter separation of the organic phase the aqueous phase
  3. extractionwas extracted with dichloromethane (3×15 ml)
  4. dry with materialThe combined organic extracts were dried over Na2SO4
  5. concentrationconcentrated to low volume

Quellen und Nachweise

ORD-Eintrag
ord-43ab929d60a9407b913402be9632b63b
Quelldatensatz
uspto-grants-2011_07
Patentnummer
US07977370B2

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