Cyclohexene → 6-Methoxy-2-morpholin-4-ylpyrid-3-ylamine
反応式
[CH3:1][O:2][C:3]1[N:8]=[C:7]([N:9]2[CH2:14][CH2:13][O:12][CH2:11][CH2:10]2)[C:6]([N+:15]([O-])=O)=[CH:5][CH:4]=1.C1CCCCC=1>[Pd].C(O)C>[CH3:1][O:2][C:3]1[N:8]=[C:7]([N:9]2[CH2:10][CH2:11][O:12][CH2:13][CH2:14]2)[C:6]([NH2:15])=[CH:5][CH:4]=1参加物
5
実験手順
6.19 g (0.026 mol) of the product 4-(6-methoxy-3-nitropyrid-2-yl)morpholine synthesized according to the above procedure, 50 ml of ethanol, 20 ml of cyclohexene and 2 g of palladium-on-charcoal were placed in a fully equipped round-bottomed flask.
出典と根拠
- ORDレコード
- ord-92bfd378b5734e0d89f5e61d774fbdaa
- 出典データセット
- uspto-grants-2005_07
- 特許番号
- US06916345B2
反応ノート
読み込み中…