Hydrochloride methanol → (2S,3S)-3-[5-(1,1-Dimethyl-4,4,4-trifluoro-2-butynyl)-2-methoxybenzyl]amino-2-phenylpiperidine dihydrochloride
反応式
C(OC([N:8]1[CH2:13][CH2:12][CH2:11][C@H:10]([NH:14][CH2:15][C:16]2[CH:21]=[C:20]([C:22]([CH3:30])([CH3:29])[C:23]#[C:24][C:25]([F:28])([F:27])[F:26])[CH:19]=[CH:18][C:17]=2[O:31][CH3:32])[C@@H:9]1[C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1)=O)(C)(C)C.[ClH:39].CO>CCOC(C)=O>[ClH:39].[ClH:39].[CH3:30][C:22]([C:20]1[CH:19]=[CH:18][C:17]([O:31][CH3:32])=[C:16]([CH:21]=1)[CH2:15][NH:14][C@H:10]1[CH2:11][CH2:12][CH2:13][NH:8][C@H:9]1[C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1)([CH3:29])[C:23]#[C:24][C:25]([F:28])([F:26])[F:27]参加物
4
反応物 2
生成物 1
試薬・触媒・溶媒 1
実験手順
To a solution of Compound 59 (34 mg, 0.064 mmol) in AcOEt (8 ml) was added an excess amount of HCl-MeOH. The mixture was stirred for 18 h and then evaporated in vacuo, the residual solid was recrystallized from MeOH-Et2O to give Compound 60 (24 mg, 75%) as a white solid.
後処理
- customevaporated in vacuo
- customthe residual solid was recrystallized from MeOH-Et2O
出典と根拠
- ORDレコード
- ord-170c32216e1e4d14986e538791dec033
- 出典データセット
- uspto-grants-2001_12
- 特許番号
- US06329396B1
反応ノート
読み込み中…