反応式
Cl[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[N:5]=[C:4]([C:12]([F:15])([F:14])[F:13])[N:3]=1.O.[NH2:17][NH2:18]>C(O)C>[NH:17]([C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[N:5]=[C:4]([C:12]([F:15])([F:14])[F:13])[N:3]=1)[NH2:18]参加物
4
実験手順
4-Chloro-2-trifluoromethylquinazoline (46.4 g, 0.2 mole) was taken up in ethanol (500 ml). Hydrazine hydrate (20 ml, 0.4 mole) was added and the contents refluxed for 2 hours. On cooling, the yellow precipitate was filtered and slurried in water (500 ml) to removed hydrazine hydrochloride. Filtration gave the product as a yellow crystalline solid, 34.5 g (76%).
後処理
- temperaturethe contents refluxed for 2 hours
- temperatureOn cooling
- filtrationthe yellow precipitate was filtered
- customto removed hydrazine hydrochloride
- filtrationFiltration
出典と根拠
- ORDレコード
- ord-660c1964dfcd4fa88cf7408a28da8c43
- 出典データセット
- uspto-grants-1994_02
- 特許番号
- US05284739
関連ノート
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