Potassium Carbonate → 3-(1-{[8-Methyl-2,3-dihydrofuro[2,3-f][1,4]benzodioxin-2-yl]methyl}-1,2,3,6-tetrahydro-4-pyridinyl)-1H-indole

HRID 1267242Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1267242
CC1C=CC(S(O[CH2:12][C@H:13]2[CH2:18][O:17][C:16]3[CH:19]=[CH:20][C:21]4OC(C)=C[C:22]=4[C:15]=3[O:14]2)(=O)=O)=CC=1.[NH:27]1[CH2:32][CH:31]=[C:30]([C:33]2[C:41]3[C:36](=[CH:37][CH:38]=[CH:39][CH:40]=3)[NH:35][CH:34]=2)[CH2:29][CH2:28]1.[C:42](=O)([O-])[O-].[K+].[K+].[O:48]1[CH2:52][CH2:51]CC1.CN(C)C=O>>[CH3:42][C:52]1[O:48][C:22]2[C:15]3[O:14][CH:13]([CH2:12][N:27]4[CH2:28][CH:29]=[C:30]([C:33]5[C:41]6[C:36](=[CH:37][CH:38]=[CH:39][CH:40]=6)[NH:35][CH:34]=5)[CH2:31][CH2:32]4)[CH2:18][O:17][C:16]=3[CH:19]=[CH:20][C:21]=2[CH:51]=1

Komponenten

5

Versuchsvorschrift

To a solution of 0.28 g (0.75 mmole) of [(2R)-8-methyl-2,3-dihydrofuro[3,2-f][1,4]benzodioxin-2-yl]methyl 4-methylbenzenesulfonate and 0.45 g (2.3 mmole) of 3-(1,2,3,6-tetrahydro-4-pyridinyl)-1H-indole in 10 mL of 1:1 tetrahydrofuran/dimethylformamide was added 1.5 g (1.1 mmole) of potassium carbonate and the mixture was refluxed under nitrogen for 15 hours. Upon cooling to room temperature, the reaction mixture was filtered and the filtrate concentrated in vacuum. The residue was column chromatographed on silica gel with 50% hexane/ethyl acetate to give 0.13 g of the (S)-enantiomer of the title compound as a yellow solid, m.p. 198-200° C.

Aufarbeitung

  1. temperaturethe mixture was refluxed under nitrogen for 15 hours
  2. filtrationthe reaction mixture was filtered
  3. concentrationthe filtrate concentrated in vacuum
  4. customchromatographed on silica gel with 50% hexane/ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-a9d6cadb4d33475884952b42f1236134
Quelldatensatz
uspto-grants-2003_04
Patentnummer
US06552049B2

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