Ethanol → 4-(4-Amino-6,7-dimethoxyquinazolin-2-yl)piperazine-1-imidic Acid Ethyl Ester
反応式
[CH2:1]([OH:3])[CH3:2].[Na].[C:5]([N:7]1[CH2:12][CH2:11][N:10]([C:13]2[N:22]=[C:21]([NH2:23])[C:20]3[C:15](=[CH:16][C:17]([O:26][CH3:27])=[C:18]([O:24][CH3:25])[CH:19]=3)[N:14]=2)[CH2:9][CH2:8]1)#[N:6]>C(O)(=O)C>[CH2:1]([O:3][C:5]([N:7]1[CH2:12][CH2:11][N:10]([C:13]2[N:22]=[C:21]([NH2:23])[C:20]3[C:15](=[CH:16][C:17]([O:26][CH3:27])=[C:18]([O:24][CH3:25])[CH:19]=3)[N:14]=2)[CH2:9][CH2:8]1)=[NH:6])[CH3:2]参加物
5
実験手順
To a dry flask equipped with stirrer, thermometer and reflux condenser is placed 25 ml. of ethanol and sodium metal, 0.253 g. (0.011 g. atom) is added in portions. When the sodium is completely reacted, 3.14 g. (0.01 mole) of 2-(4-cyanopiperazin-1-yl)-4-amino-6,7-dimethoxyquinazoline is added and the resulting mixture is refluxed for 5 hours. After cooling to room temperature, glacial acetic acid is added to neutralize the mixture. After evaporation to dryness, 25 ml. of water and 50 ml. of chloroform are added to the residue. The mixture is transferred to a separatory funnel and the chloroform layer washed again with water, dried over anhydrous sodium sulfate then concentrated to dryness to provide the title compound.
後処理
- customTo a dry flask equipped with stirrer
- temperaturethermometer and reflux condenser
- addition(0.011 g. atom) is added in portions
- temperaturethe resulting mixture is refluxed for 5 hours
- customAfter evaporation to dryness, 25 ml
- additionof chloroform are added to the residue
- customThe mixture is transferred to a separatory funnel
- washthe chloroform layer washed again with water
- dry with materialdried over anhydrous sodium sulfate
- concentrationthen concentrated to dryness
出典と根拠
- ORDレコード
- ord-48208be7e38f41ac839ecf78dbd7004c
- 出典データセット
- uspto-grants-1977_12
- 特許番号
- US04062844
反応ノート
読み込み中…