Sodium Carbonate → HCID 86748237, Verbindung

HRID 2379444Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2379444
[CH2:1]1[C@@H:6]2[C:7]3[CH:19]=[CH:18][CH:17]=[CH:16][C:8]=3[CH2:9][C:10]3[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=3[N:5]2[CH2:4][CH2:3][NH:2]1.Cl[CH2:21][CH2:22][O:23][CH2:24][C:25]([O:27][CH2:28][CH3:29])=[O:26].C(=O)([O-])[O-].[Na+].[Na+]>[I-].[Na+].CC(C)CC(=O)C>[CH2:1]1[C@@H:6]2[C:7]3[CH:19]=[CH:18][CH:17]=[CH:16][C:8]=3[CH2:9][C:10]3[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=3[N:5]2[CH2:4][CH2:3][N:2]1[CH2:21][CH2:22][O:23][CH2:24][C:25]([O:27][CH2:28][CH3:29])=[O:26]

Komponenten

6

Versuchsvorschrift

32.48 g of (S)-1,2,3,4,10,14b-hexahydrodibenzo[c,f]pyrazino[1,2-a]azepine (prepared as described in Preparation 3), 22.7 g of ethyl 2-chloroethoxyacetate, 48.9 g of sodium carbonate and 0.79 g of sodium iodide were added to 340 ml of 4-methyl-2-pentanone, and the mixture was heated under reflux for 16 hours. At the end of this time, it was cooled to room temperature and was filtered using a Celite filter aid, and the filtrate was concentrated by evaporation under reduced pressure. The resulting residue was subjected to column chromatography through silica gel eluted with a 1:1 by volume mixture of ethyl acetate and hexane, to give 44.85 g (yield 91%) of the title compound as a pale yellow oil.

Aufarbeitung

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 16 hours
  3. filtrationwas filtered
  4. filtrationfilter aid
  5. concentrationthe filtrate was concentrated by evaporation under reduced pressure
  6. washeluted with a 1:1 by volume mixture of ethyl acetate and hexane

Quellen und Nachweise

ORD-Eintrag
ord-b875e032fc4549799fc97eb4dfef0786
Quelldatensatz
uspto-grants-1994_11
Patentnummer
US05362725

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