反応式
[NH2:1][C:2]1([CH2:17][CH3:18])[C:7](=[O:8])[N:6]([CH:9]2[CH2:14][CH2:13][CH2:12][CH2:11][CH2:10]2)[C:5](=[O:15])[NH:4][C:3]1=[O:16].C(N1C(=O)C(C)(N2[C:36](=[O:37])[C:35]3[C:30](=[C:31]([F:41])[C:32]([F:40])=[C:33]([F:39])[C:34]=3[F:38])[C:29]2=[O:42])C(=O)NC1=O)C>>[CH:9]1([N:6]2[C:7](=[O:8])[C:2]([CH2:17][CH3:18])([N:1]3[C:29](=[O:42])[C:30]4[C:35](=[C:34]([F:38])[C:33]([F:39])=[C:32]([F:40])[C:31]=4[F:41])[C:36]3=[O:37])[C:3](=[O:16])[NH:4][C:5]2=[O:15])[CH2:14][CH2:13][CH2:12][CH2:11][CH2:10]1参加物
3
反応物 2
生成物 1
実験手順
Compound 19i was prepared from 5-amino-1-cyclohexyl-5-ethylbarbituric acid (0.38 g, 1.50 mmol) using the same procedure described for 19f. The crude product was recrystallized from EtOH to give 1-cyclohexyl-5-ethyl-5-(tetrafluorophthalimido)barbituric acid (19i) as white crystals.
後処理
- customThe crude product was recrystallized from EtOH
出典と根拠
- ORDレコード
- ord-de55129afb3543618c7987d87d1d81a1
- 出典データセット
- uspto-grants-2012_03
- 特許番号
- US08143252B2
関連ノート
読み込み中…