4-Fluoro-N-methylaniline → N'-{[4-(3,4-Dichlorobenzyl)morpholin-2-yl]methyl}-N-(4-fluorophenyl)-N-methylurea
反応式
[F:1][C:2]1[CH:9]=[CH:8][C:5]([NH:6][CH3:7])=[CH:4][CH:3]=1.[Cl:10][C:11]1[CH:12]=[C:13]([CH:35]=[CH:36][C:37]=1[Cl:38])[CH2:14][N:15]1[CH2:20][CH2:19][O:18][CH:17]([CH2:21][NH:22][C:23](=[O:34])OC2C=CC([N+]([O-])=O)=CC=2)[CH2:16]1>N1C=CC=CC=1>[Cl:10][C:11]1[CH:12]=[C:13]([CH:35]=[CH:36][C:37]=1[Cl:38])[CH2:14][N:15]1[CH2:20][CH2:19][O:18][CH:17]([CH2:21][NH:22][C:23](=[O:34])[N:6]([C:5]2[CH:8]=[CH:9][C:2]([F:1])=[CH:3][CH:4]=2)[CH3:7])[CH2:16]1参加物
4
反応条件
- 温度
- 110 °C
実験手順
4-Fluoro-N-methylaniline (0.007 ml) was added to a solution of Intermediate 10 (0.025 g) in anhydrous pyridine (1 ml). The mixture was heated at 110° C. in a thick walled glass vial (Reactivial) for 20 h. The mixture was evaporated to remove the pyridine, and partitioned between ethyl acetate (10 ml) and saturated aqueous sodium bicarbonate solution (10 ml). The organic layer was washed with further sodium bicarbonate (10 ml×5), brine (10 ml), dried (MgSO4), concentrated in vacuo. The residue was purified by chromatography on silica gel (Trikonex flash tube 2002, 2 g), eluting with 70% ethyl acetate in cyclohexane to give the title compound as a pale yellow gum 0.014 g. LCMS (system A) Rt 2.52 min, Mass Spectrum m/z 426 [MH+].