3-Chloro-6-(3-fluoro-4-methoxyphenyl)pyridazine → [1-(1-Ethylpropyl)piperidin-4-yl]-[6-(3-fluoro-4-methoxyphenyl)pyridazin-3-yl]amine
反応式
Cl[C:2]1[N:3]=[N:4][C:5]([C:8]2[CH:13]=[CH:12][C:11]([O:14][CH3:15])=[C:10]([F:16])[CH:9]=2)=[CH:6][CH:7]=1.[NH2:17][CH:18]1[CH2:23][CH2:22][N:21]([CH:24]([CH2:27][CH3:28])[CH2:25][CH3:26])[CH2:20][CH2:19]1>>[CH2:25]([CH:24]([N:21]1[CH2:22][CH2:23][CH:18]([NH:17][C:2]2[N:3]=[N:4][C:5]([C:8]3[CH:13]=[CH:12][C:11]([O:14][CH3:15])=[C:10]([F:16])[CH:9]=3)=[CH:6][CH:7]=2)[CH2:19][CH2:20]1)[CH2:27][CH3:28])[CH3:26]参加物
3
実験手順
The title compound was prepared by a similar procedure to that described in Example 1, starting from 3-chloro-6-(4-methoxy-3-fluorophenyl)pyridazine and 4-amino-1-(1-ethylpropyl)piperidine.
出典と根拠
- ORDレコード
- ord-b5da02f55a884a8ca7fd8fb3c0fb97ff
- 出典データセット
- uspto-grants-2013_08
- 特許番号
- US08501739B2
反応ノート
読み込み中…