反応式
C[N:2]([CH3:15])[CH:3]=[CH:4][C:5]([C:7]1[CH:12]=[CH:11][CH:10]=[C:9]([O:13][CH3:14])[CH:8]=1)=O.Cl.NC1[N:19]=[CH:20][NH:21][C:22]=1[C:23]([NH2:25])=[O:24].C(#N)C.C(O)C>C(O)(=O)C>[CH3:14][O:13][C:9]1[CH:8]=[C:7]([C:5]2[N:19]3[CH:20]=[N:21][C:22]([C:23]([NH2:25])=[O:24])=[C:15]3[N:2]=[CH:3][CH:4]=2)[CH:12]=[CH:11][CH:10]=1参加物
6
実験手順
A stirred mixture of 15.0 g of 3-dimethylamino-3'-methoxyacrylophenone (prepared as described in Example 5 and 9.2 g of 4-amino-5-imidazolecarboxamide hydrochloride in 150 ml of glacial acetic acid was heated at reflux for 24 hours. The solvent was evaporated in vacuo and the crystalline residue was treated with 100 ml of saturated sodium bicarbonate solution, filtered and washed with 200 ml of water to give yellow crystals. This material was treated with 400 ml of acetonitrile then with 600 ml of hot ethanol to give 9.9 g of the product of the example as yellow crystals, mp 249°-252° C.
後処理
- customprepared
- temperaturewas heated
- temperatureat reflux for 24 hours
- customThe solvent was evaporated in vacuo
- additionthe crystalline residue was treated with 100 ml of saturated sodium bicarbonate solution
- filtrationfiltered
- washwashed with 200 ml of water
- customto give yellow crystals
出典と根拠
- ORDレコード
- ord-73767f1bc2024c24a26597c6068287f1
- 出典データセット
- uspto-grants-1989_12
- 特許番号
- US04888345
関連ノート
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