Potassium Carbonate → 2-(4-{5-[1,1,1,3,3,3-Hexafluoro-2-(4-methoxybenzyloxy)propan-2-yl]-4-propylpyridin-2-yl}piperazin-1-yl)ethanol
反応式
C([O:4][CH2:5][CH2:6][N:7]1[CH2:12][CH2:11][N:10]([C:13]2[CH:18]=[C:17]([CH2:19][CH2:20][CH3:21])[C:16]([C:22]([O:31][CH2:32][C:33]3[CH:38]=[CH:37][C:36]([O:39][CH3:40])=[CH:35][CH:34]=3)([C:27]([F:30])([F:29])[F:28])[C:23]([F:26])([F:25])[F:24])=[CH:15][N:14]=2)[CH2:9][CH2:8]1)(=O)C.C(=O)([O-])[O-].[K+].[K+]>CO>[F:25][C:23]([F:24])([F:26])[C:22]([C:16]1[C:17]([CH2:19][CH2:20][CH3:21])=[CH:18][C:13]([N:10]2[CH2:11][CH2:12][N:7]([CH2:6][CH2:5][OH:4])[CH2:8][CH2:9]2)=[N:14][CH:15]=1)([O:31][CH2:32][C:33]1[CH:34]=[CH:35][C:36]([O:39][CH3:40])=[CH:37][CH:38]=1)[C:27]([F:30])([F:29])[F:28]参加物
4
反応物 2
生成物 1
試薬・触媒・溶媒 1
実験手順
2-(4-{5-[1,1,1,3,3,3-Hexafluoro-2-(4-methoxybenzyloxy)propan-2-yl]-4-propylpyridin-2-yl}piperazin-1-yl)ethyl acetate (479 mg) was dissolved in methanol (2.3 mL), added potassium carbonate (127 mg, 0.722 mmol), and the mixture was stirred at room temperature for 0.5 hours. The reaction solution was concentrated in vacuo. The obtained residue was purified by silica-gel column chromatography (chloroform/methanol). The title compound (117 mg (yield 47%)) was obtained as a yellow oil.
後処理
- concentrationThe reaction solution was concentrated in vacuo
- customThe obtained residue was purified by silica-gel column chromatography (chloroform/methanol)
出典と根拠
- ORDレコード
- ord-05a5d8d831ed420085abd5451819a7d8
- 出典データセット
- uspto-grants-2013_10
- 特許番号
- US08551985B2
反応ノート
読み込み中…