Hydrazine hydrate (1:1) → 2-Chloro-3-hydrazino-6-methoxyquinoxaline
反応式
[Cl:1][C:2]1[C:11](Cl)=[N:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([O:13][CH3:14])[CH:8]=2)[N:3]=1.O.[NH2:16][NH2:17]>C(O)C>[Cl:1][C:2]1[C:11]([NH:16][NH2:17])=[N:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([O:13][CH3:14])[CH:8]=2)[N:3]=1参加物
4
実験手順
2,3-Dichloro-6-methoxyquinoxaline (4.2 g., 0.018 mole), the product of Preparation E(b), and 2.7 ml. of hydrazine hydrate in 100 ml. of ethanol were heated under reflux for 4 hours and stirred at room temperature overnight. The precipitate was removed by filtration and washed with ethanol to afford 3.9 g. (97% yield) of 2-chloro-3-hydrazino-6-methoxyquinoxaline, m.p. <250° C. Mass spectrum: m/e, 224 (P); m/e 226 (P+2).
後処理
- temperatureunder reflux for 4 hours
- customThe precipitate was removed by filtration
- washwashed with ethanol
- customto afford 3.9 g
出典と根拠
- ORDレコード
- ord-23598780aee6489080400c6462e25ea0
- 出典データセット
- uspto-grants-1985_01
- 特許番号
- US04495187
反応ノート
読み込み中…