Dimethylethylamine → (2-{[2-(4-Ethoxy-3-methoxyphenyl)ethyl]amino}ethyl){2-methyl-6-[(2,4,6-trimethylphenyl)amino]pyrimidin-4-yl}amine
反応式
[CH2:1]([O:3][C:4]1[CH:9]=[CH:8][C:7]([CH2:10][C:11]([NH:13][CH2:14][CH2:15][NH:16][C:17]2[CH:22]=[C:21]([NH:23][C:24]3[C:29]([CH3:30])=[CH:28][C:27]([CH3:31])=[CH:26][C:25]=3[CH3:32])[N:20]=[C:19]([CH3:33])[N:18]=2)=O)=[CH:6][C:5]=1[O:34][CH3:35])[CH3:2].[AlH3].N(CC)(C)C>C1COCC1>[CH2:1]([O:3][C:4]1[CH:9]=[CH:8][C:7]([CH2:10][CH2:11][NH:13][CH2:14][CH2:15][NH:16][C:17]2[CH:22]=[C:21]([NH:23][C:24]3[C:25]([CH3:32])=[CH:26][C:27]([CH3:31])=[CH:28][C:29]=3[CH3:30])[N:20]=[C:19]([CH3:33])[N:18]=2)=[CH:6][C:5]=1[O:34][CH3:35])[CH3:2]参加物
5
反応物 3
生成物 1
試薬・触媒・溶媒 1
実験手順
Heat a solution of 2-(4-ethoxy-3-methoxy-phenyl)-N-{2-[2-methyl-6-(2,4,6-trimethyl-phenylamino)-pyrimidin-4-ylamino]ethyl}-acetamide (0.324 g, 0.68 mmol) in THF (10 mL) with AlH3.NMe2Et (14 mL, 6.78 mmol) to reflux for 14 h. Cool the resulting mixture to ambient temperature, quench with Na2CO3.10H2O (1.0 g) and stir at ambient temperature for 15 min. Filter the solution through Celite and wash with several portions of CH2Cl2. Concentrate the filtrate in vacuo to dryness and purify by preparative TLC (10% MeOH in CH2Cl2) to obtain the title compound.
後処理
- customquench with Na2CO3.10H2O (1.0 g)
- filtrationFilter the solution through Celite
- washwash with several portions of CH2Cl2
- concentrationConcentrate the filtrate in vacuo to dryness
- custompurify by preparative TLC (10% MeOH in CH2Cl2)
出典と根拠
- ORDレコード
- ord-310bc6bdd1744f3698d1fda06b60b62d
- 出典データセット
- uspto-grants-2004_02
- 特許番号
- US06696445B2
反応ノート
読み込み中…