Ammonia → 3-Amino-6-(3-trifluoromethylphenyl)pyridazine
反応式
Cl[C:2]1[N:3]=[N:4][C:5]([C:8]2[CH:13]=[CH:12][CH:11]=[C:10]([C:14]([F:17])([F:16])[F:15])[CH:9]=2)=[CH:6][CH:7]=1.[NH3:18]>>[NH2:18][C:2]1[N:3]=[N:4][C:5]([C:8]2[CH:13]=[CH:12][CH:11]=[C:10]([C:14]([F:17])([F:16])[F:15])[CH:9]=2)=[CH:6][CH:7]=1参加物
3
反応条件
- 温度
- 200 °C
実験手順
A 12.5 g sample of 3-chloro-6-[3-(trifluoromethyl)phenyl]pyridazine was placed in a steel cylinder with liquid ammonia and the sealed cylinder (bomb) was heated at 200° C. The chilled cylinder was opened and the ammonia allowed to evaporate. The solid residue was heated and stirred with chloroform, then filtered. The filtrate was concentrated and the residue recrystallized, first from chloroform-hexane, then twice from chloroform to give 1.8 g of 3-amino-6-[3-(trifluoromethyl)phenyl]pyridazine as white crystals, mp 143°-145° C.
後処理
- customto evaporate
- temperatureThe solid residue was heated
- filtrationfiltered
- concentrationThe filtrate was concentrated
- customthe residue recrystallized, first from chloroform-hexane
出典と根拠
- ORDレコード
- ord-249344310eed46bab2a8f1c73e2d6122
- 出典データセット
- uspto-grants-1986_02
- 特許番号
- US04569934
反応ノート
読み込み中…