反応式
[N:1]1([CH2:6][CH2:7][CH2:8][NH2:9])[CH:5]=[CH:4][N:3]=[CH:2]1.[CH:10](=[O:17])C1C=CC=CC=1.[CH2:18]([N+]#[C-])[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1.[O:27]([C:29]#[N:30])[K]>>[N:1]1([CH2:6][CH2:7][CH2:8][N:9]2[CH:18]([C:19]3[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=3)[C:29](=[O:27])[NH:30][C:10]2=[O:17])[CH:5]=[CH:4][N:3]=[CH:2]1参加物
5
実験手順
The compound was synthesized starting from 3-(1H-imidazol-1-yl)propylamine 1.0 g (7.98 mmol), benzaldehyde 0.807 ml (7.98 mmol), benzylisonitrile 0.972 ml (7.98 mmol), pyidiniumchloride 0.920 and KOCN 0.648 g (7.98 mmol) as described in method 1.
後処理
- customThe compound was synthesized
出典と根拠
- ORDレコード
- ord-6a6efb9c2d1e4baa83497ba8bbbb9625
- 出典データセット
- uspto-grants-2014_11
- 特許番号
- US08889709B2
関連ノート
読み込み中…