2-ethyl-5-fluoro-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indole → 2-ethyl-5-fluoro-3-piperidin-4-yl-1H-indole
反応式
[CH2:1]([C:3]1[NH:4][C:5]2[C:10]([C:11]=1[C:12]1[CH2:13][CH2:14][NH:15][CH2:16][CH:17]=1)=[CH:9][C:8]([F:18])=[CH:7][CH:6]=2)[CH3:2]>CO.[Pd]>[CH2:1]([C:3]1[NH:4][C:5]2[C:10]([C:11]=1[CH:12]1[CH2:13][CH2:14][NH:15][CH2:16][CH2:17]1)=[CH:9][C:8]([F:18])=[CH:7][CH:6]=2)[CH3:2]参加物
4
実験手順
2.83 g 2-ethyl-5-fluoro-3-(1.2.3.6-tetrahydropyridin-4-yl)-1H-indole are suspended in 50 ml of methanol and hydrogenated with 0.3 g Pd/C 10% at normal pressure and ambient temperature. The catalyst is suction filtered and the filtrate is evaporated to dryness. 2.3 g (V-1) are obtained in the form of a solid. 1H NMR (400 MHz, DMSO): 2.70 (2H, q); 1.19 (3H, t).
後処理
- filtrationfiltered
- customthe filtrate is evaporated to dryness
- custom2.3 g (V-1) are obtained in the form of a solid
出典と根拠
- ORDレコード
- ord-79c35a453f9d4479bdd54efc09d2ea0f
- 出典データセット
- uspto-grants-2015_10
- 特許番号
- US09161927B2
反応ノート
読み込み中…