Reaktion #3772

ord-f3c835216c0344d1af2af2f75940e898

Reaktionsgleichung

O=C([O-])O.[Na+]
sodium bicarbonate
O=S(=O)(O)O
sulfuric acid
O=C(OC(=O)C(F)(F)F)C(F)(F)F
trifluoroacetic anhydride
O=C([C@H](Cc1ccccc1)N1C(=O)c2ccccc2C1=O)N1C=CCC=C1
(S)-N-[2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-oxo-3-phenylpropyl]-1,4-dihydro-pyridine
O=C1[C@@H](N2C(=O)c3ccccc3C2=O)Cc2ccccc2C2CCC=CN12
title compound
O=C1[C@@H](N2C(=O)c3ccccc3C2=O)Cc2ccccc2C2CCC=CN12
(S)-7-[(1,3-Dihydro-1,3-dioxo-2H-isoindol-2-yl)]-1,2,6,7,8,12b-hexahydro-6-oxopyrido[2,1-a][2]benzazepine

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONpour the reaction mixture
  2. 2
    ExtraktionExtract with ethyl acetate
  3. 3
    Filtrationfilter through a plug of silica gel
  4. 4
    WaschenRinse the silica gel with dichloromethane
  5. 5
    SonstigeEvaporate the filtrate in vacuo
  6. 6
    Sonstigeto give a residue

Vorschrift

Combine sulfuric acid (3.0 mL, 96%) and trifluoroacetic anhydride (300 mL). Add (S)-N-[2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-oxo-3-phenylpropyl]-1,4-dihydro-pyridine (1.0 mmol). After 30 minutes, pour the reaction mixture into a mixture of saturated aqueous sodium bicarbonate and ice. Extract with ethyl acetate and then with methylene chloride. Combine the organic layers and filter through a plug of silica gel. Rinse the silica gel with dichloromethane. Evaporate the filtrate in vacuo to give a residue. Chromatograph the residue on silica gel eluting sequentially with 10% ethyl acetate/hexane and then 25% ethyl acetate/hexane to give the title compound.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05734049uspto-grants-1998_03