Triethylamine → Methyl bis-(cyclohexylmethyl)acetyl-(alpha-methyl-D-tryptophan)

HRID 976053Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 976053
C[NH:2][C@@:3]([CH3:17])([C:14]([OH:16])=[O:15])[CH2:4][C:5]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[NH:7][CH:6]=1.[CH:18]1([CH2:24][CH:25]([CH2:29][CH:30]2[CH2:35][CH2:34][CH2:33][CH2:32][CH2:31]2)[C:26](Cl)=[O:27])[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]1.[CH3:36]CN(CC)CC>C1COCC1.CCOC(C)=O>[CH3:36][C:25]([CH2:29][CH:30]1[CH2:35][CH2:34][CH2:33][CH2:32][CH2:31]1)([CH2:24][CH:18]1[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]1)[C:26]([NH:2][C@@:3]([CH3:17])([C:14]([OH:16])=[O:15])[CH2:4][C:5]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[NH:7][CH:6]=1)=[O:27]

Komponenten

6

Versuchsvorschrift

To a solution of 0.69 g (3.0 mmol) of methyl α-methyl-D-tryptophan in 20 mL THF was added 0.8 g (3.0 mmol) of bis-(cyclohexylmethyl)acetyl chloride followed by 0.5 mL of Et3N and the suspension stirred at room temperature for 3 days. The mixture was diluted with EtOAc and washed with 1N citric acid, H2O, and saturated NaCl. Drying over MgSO4 and removal of the solvent under reduced pressure left 1.4 g of the crude product as a foam. Chromatography on silica gel, eluting with CHCl3 /EtOAc (95/5) gave 0.91 g (65% yield) of the product as a white foam. The structure was confirmed by NMR and mass spectroscopy.

Aufarbeitung

  1. washwashed with 1N citric acid, H2O, and saturated NaCl
  2. dry with materialDrying over MgSO4 and removal of the solvent under reduced pressure
  3. waitleft 1.4 g of the crude product as a foam
  4. washChromatography on silica gel, eluting with CHCl3 /EtOAc (95/5)

Quellen und Nachweise

ORD-Eintrag
ord-9702d1d0a4924757ac1441109fbcf099
Quelldatensatz
uspto-grants-1997_03
Patentnummer
US05610177

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