2,6-Dichloropyrazine → 4-(6-Chloropyrazin-2-yl)piperazin-2-one
反応式
Cl[C:2]1[CH:7]=[N:6][CH:5]=[C:4]([Cl:8])[N:3]=1.[O:9]=[C:10]1[CH2:15][NH:14][CH2:13][CH2:12][NH:11]1>C(#N)C>[Cl:8][C:4]1[N:3]=[C:2]([N:14]2[CH2:13][CH2:12][NH:11][C:10](=[O:9])[CH2:15]2)[CH:7]=[N:6][CH:5]=1参加物
4
実験手順
A mixture of 10.0 g (0.0067 mole) of 2,6-dichloropyrazine and 14 g (0.14 mole) of 2-oxopiperazine in 100 ml of acetonitrile is refluxed 1.5 hour with stirring under N2. The mixture is concentrated under vacuum, the residue titrated with water and filtered, and the crude solid recrystallized from water (charcoal treatment) to give off-white plates of the subject compound, 7.7 g, mp 192°-193° C.
後処理
- temperatureis refluxed 1.5 hour
- concentrationThe mixture is concentrated under vacuum
- filtrationfiltered
- customthe crude solid recrystallized from water (charcoal treatment)
- customto give off-white plates of the subject compound, 7.7 g, mp 192°-193° C.
出典と根拠
- ORDレコード
- ord-fbaa38e21c5b4138988186de4e3cf619
- 出典データセット
- uspto-grants-1979_08
- 特許番号
- US04163849
反応ノート
読み込み中…