Ethanol → 4-(4-Amino-6,7-dimethoxyquinazolin-2-yl)piperazine-1-imidic Acid Ethyl Ester

HRID 461333ノート

反応式

HRID 461333 の反応式
[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

  1. customTo a dry flask equipped with stirrer
  2. temperaturethermometer and reflux condenser
  3. addition(0.011 g. atom) is added in portions
  4. temperaturethe resulting mixture is refluxed for 5 hours
  5. customAfter evaporation to dryness, 25 ml
  6. additionof chloroform are added to the residue
  7. customThe mixture is transferred to a separatory funnel
  8. washthe chloroform layer washed again with water
  9. dry with materialdried over anhydrous sodium sulfate
  10. 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

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