Hydrazine → HCID 86752611、化合物
反応式
[F:1][C:2]([F:19])([F:18])[C:3]([C:5]1[N:13]2[C:8]([CH:9]=[CH:10][CH:11]=[CH:12]2)=[CH:7][C:6]=1[C:14](OC)=[O:15])=O.[NH2:20][NH2:21]>C(O)C>[F:1][C:2]([F:19])([F:18])[C:3]1[C:5]2[N:13]3[C:8]([CH:9]=[CH:10][CH:11]=[CH:12]3)=[CH:7][C:6]=2[C:14](=[O:15])[NH:21][N:20]=1参加物
4
実験手順
A mixture of (I) (3.60 g, 13.3 mmol) and excess 85% aqueous hydrazine in ethanol (250 mL) was heated under reflux for 10 minutes (a precipitate formed). After cooling in a freezer overnight, the solid was collected by filtration and dried to give 4-trifluoromethylpyridazino[4,5-b]indolizin-1-one (II, 2.65 g, 79%)
後処理
- temperaturewas heated
- temperatureunder reflux for 10 minutes (a precipitate
- customformed)
- temperatureAfter cooling in a freezer overnight
- filtrationthe solid was collected by filtration
- customdried
出典と根拠
- ORDレコード
- ord-6355edc7f834451f8e7e42803161cd21
- 出典データセット
- uspto-grants-1998_05
- 特許番号
- US05756501
反応ノート
読み込み中…