Hydrochloric Acid → 2-[3,5-Bis(trifluoromethyl)phenyl]-n{4-(5-fluoro-2-methylphenyl)-6-[(7s,9as)-7-(hydroxymethyl)hexahydropyrazino[2,1-c][1,4]oxazin-8(1h)-yl]-3-pyridinyl}-n,2-dimethylpropanamide hydrochloride
反応式
[ClH:1].[F:2][C:3]([F:48])([F:47])[C:4]1[CH:5]=[C:6]([C:14]([CH3:46])([CH3:45])[C:15]([N:17]([C:19]2[CH:20]=[N:21][C:22]([N:33]3[C@H:42]([CH2:43][OH:44])[CH2:41][N:40]4[C@H:35]([CH2:36][O:37][CH2:38][CH2:39]4)[CH2:34]3)=[CH:23][C:24]=2[C:25]2[CH:30]=[C:29]([F:31])[CH:28]=[CH:27][C:26]=2[CH3:32])[CH3:18])=[O:16])[CH:7]=[C:8]([C:10]([F:13])([F:12])[F:11])[CH:9]=1>>[ClH:1].[F:12][C:10]([F:11])([F:13])[C:8]1[CH:7]=[C:6]([C:14]([CH3:46])([CH3:45])[C:15]([N:17]([C:19]2[CH:20]=[N:21][C:22]([N:33]3[C@H:42]([CH2:43][OH:44])[CH2:41][N:40]4[C@H:35]([CH2:36][O:37][CH2:38][CH2:39]4)[CH2:34]3)=[CH:23][C:24]=2[C:25]2[CH:30]=[C:29]([F:31])[CH:28]=[CH:27][C:26]=2[CH3:32])[CH3:18])=[O:16])[CH:5]=[C:4]([C:3]([F:2])([F:48])[F:47])[CH:9]=1参加物
3
反応物 2
生成物 1
実験手順
HCl salt made according to method described in Example 41 starting from 2-[3,5-bis(trifluoromethyl)phenyl]-N-{4-(5-fluoro-2-methylphenyl)-6-[(7S,9aS)-7-(hydroxymethyl)hexahydropyrazino[2,1-c][1,4]oxazin-8(1H)-yl]-3-pyridinyl}-N,2-dimethylpropanamide (E45, 11.5 mg) to afford a pale yellow solid
後処理
- customto afford a pale yellow solid
出典と根拠
- ORDレコード
- ord-4d3f45f997624c1fbf1eeccbed118645
- 出典データセット
- uspto-grants-2011_04
- 特許番号
- US07919491B2
反応ノート
読み込み中…