Reaktion #46806

ord-11753aeeb2984b2f8a99a7765cca0429

Reaktionsgleichung

Nc1ccc(N2CCOCC2=O)cc1
4-(4-amino-phenyl)-morpholin-3-one
O=C([O-])O.[Na+]
NaHCO3
O
H2O
COC(=O)c1cccc2[nH]c(C(Cl)(Cl)Cl)nc12
methyl-2-trichloromethyl-1H-benzoimidazole-4-carboxylate
COC(=O)c1cccc2[nH]c(C(=O)Nc3ccc(N4CCOCC4=O)cc3)nc12
2-[4-(3-Oxo-morpholin-4-yl)-phenylcarbamoyl]-1H-benzoimidazole-4-carboxylic acid methyl ester

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Waschenwashed with 30 mL of a saturated NaHCO3-solution
  2. 2
    ExtraktionThe aqueous solution was extracted with 50 mL CH2Cl2
  3. 3
    Trocknenthe combined organic layers were dried over MgSO4
  4. 4
    Einengenconcentrated under reduced pressure
  5. 5
    Sonstigeto give a brown solid, which

Vorschrift

A solution of 69.4 mg (0.236 mmol) methyl-2-trichloromethyl-1H-benzoimidazole-4-carboxylate in 2 mL THF were slowly added to a mixture containing 50 mg (0.26 mmol) 4-(4-amino-phenyl)-morpholin-3-one, 220 mg (2.62 mmol) NaHCO3, 8 mL THF and 3 mL H2O. The mixture was stirred vigorously for 3 h at room temperature, diluted with 50 mL CH2Cl2 and washed with 30 mL of a saturated NaHCO3-solution. The aqueous solution was extracted with 50 mL CH2Cl2 and the combined organic layers were dried over MgSO4 and concentrated under reduced pressure to give a brown solid, which was pure enough for the following reactions.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07741341B2uspto-grants-2010_06