반응 #46900

ord-87f27d586a1c44ff9b958c8c69d2a23d

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    세척washed with a saturated NaHCO3-solution and with brine
  2. 2
    건조The organic layer was dried over anhydrous MgSO4
  3. 3
    농축concentrated under reduced pressure
  4. 4
    기타After purification by preparative RP-HPLC (CH3CN/H2O gradient and 0.05% formic acid) pure 2-[2-Fluoro-4-(pyrrolidine-1-carbonyl)-phenylcarbamoyl]-1H-benzoimidazole-4-carboxylic acid methyl ester
  5. 5
    기타was obtained in form of a colorless amorphous solid

실험 절차

59.0 mg (0.28 mmol) (4-Amino-3-fluoro-phenyl)-pyrrolidin-1-yl-methanone was dissolved in 6 mL THF and 3 mL water. 238.0 mg (2.83 mmol) NaHCO3 were added. Finally 75.6 mg (0.26 mmol) 2-Trichloromethyl-1H-benzoimidazole-4-carboxylic acid methyl ester were added and the resulting mixture was stirred vigorously for 3 h at RT. The mixture was diluted with 25 mL CH2Cl2 and washed with a saturated NaHCO3-solution and with brine. The organic layer was dried over anhydrous MgSO4 and concentrated under reduced pressure. After purification by preparative RP-HPLC (CH3CN/H2O gradient and 0.05% formic acid) pure 2-[2-Fluoro-4-(pyrrolidine-1-carbonyl)-phenylcarbamoyl]-1H-benzoimidazole-4-carboxylic acid methyl ester was obtained in form of a colorless amorphous solid.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07741341B2uspto-grants-2010_06