反応式
Cl[C:2]1[N:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[NH:8][C:7](=[O:12])[C:6]([C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)=[CH:5]2.O.[NH2:20][NH2:21].CCOCC.O>N1C=CC=CC=1>[NH:20]([C:2]1[N:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[NH:8][C:7](=[O:12])[C:6]([C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)=[CH:5]2)[NH2:21]参加物
6
反応条件
- 温度
- 160 °C
実験手順
A mixture of 6-chloro-3-phenyl-1,5-naphthyridin-2(1H)-one (7-1) (1.4 g, 5.61 mmol) and hydrazine hydrate (2 g, 40 mmol) in pyridine (18 mL) was heated under microwave irradiation at 160° C. for 1.5 hours. To the mixture was added Et2O and water, and the resulting solid was collected by filtration to give 6-hydrazino-3-phenyl-1,5-naphthyridin-2(1H)one (7-2) as orange solid.
後処理
- filtrationthe resulting solid was collected by filtration
出典と根拠
- ORDレコード
- ord-1743d55a84284d259933a725ef93c5da
- 出典データセット
- uspto-grants-2013_09
- 特許番号
- US08536193B2
関連ノート
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