2,4-Dimethoxybenzylamine → 4-Tert-butyl 2-methyl 2-((2,4-dimethoxybenzylamino)methyl)morpholine-2,4-dicarboxylate
反応式
S(O[CH2:12][C:13]1([C:26]([O:28][CH3:29])=[O:27])[O:18][CH2:17][CH2:16][N:15]([C:19]([O:21][C:22]([CH3:25])([CH3:24])[CH3:23])=[O:20])[CH2:14]1)(C1C=CC(C)=CC=1)(=O)=O.[CH3:30][O:31][C:32]1[CH:37]=[C:36]([O:38][CH3:39])[CH:35]=[CH:34][C:33]=1[CH2:40][NH2:41]>C(#N)C>[CH3:30][O:31][C:32]1[CH:37]=[C:36]([O:38][CH3:39])[CH:35]=[CH:34][C:33]=1[CH2:40][NH:41][CH2:12][C:13]1([C:26]([O:28][CH3:29])=[O:27])[O:18][CH2:17][CH2:16][N:15]([C:19]([O:21][C:22]([CH3:23])([CH3:24])[CH3:25])=[O:20])[CH2:14]1参加物
4
実験手順
E4 (365 mg, 0.850 mmol) was dissolved in acetonitrile (10 mL), (2,4-dimethoxyphenyl)methanamine (700 μL, 4.66 mmol) was added and the solution was stirred for 15 h at reflux temperature. The reaction mixture was concentrated in vacuo, extracted with water/EtOAc and washed twice with water. The organic layer was washed with brine, dried over MgSO4, filtered and concentrated in vacuo. The residue was purified by flash column chromatography from toluene:EtOAc 100:0 to 20:80 which gave the title compound (115 mg, 32%). MS (ES) C21H32N2O7 requires: 424. found: 425.2 [M+H]+.
後処理
- temperatureat reflux temperature
- concentrationThe reaction mixture was concentrated in vacuo
- extractionextracted with water/EtOAc
- washwashed twice with water
- washThe organic layer was washed with brine
- dry with materialdried over MgSO4
- filtrationfiltered
- concentrationconcentrated in vacuo
- customThe residue was purified by flash column chromatography from toluene:EtOAc 100:0 to 20:80 which
出典と根拠
- ORDレコード
- ord-07f5e08bbb254584908b0b4b39998a05
- 出典データセット
- uspto-grants-2015_08
- 特許番号
- US09102676B2
反応ノート
読み込み中…