Potassium Iodide → 4-{4-[4-(3,3-Dimethyl-butyl)-piperazin-1-yl]-butoxy}-3-fluoro-benzoic Acid Ethyl Ester
反応式
Cl.[CH3:2][C:3]([CH3:13])([CH3:12])[CH2:4][CH2:5][N:6]1[CH2:11][CH2:10][NH:9][CH2:8][CH2:7]1.C(=O)([O-])[O-].[K+].[K+].[I-].[K+].[CH2:22]([O:24][C:25](=[O:39])[C:26]1[CH:31]=[CH:30][C:29]([O:32][CH2:33][CH2:34][CH2:35][CH2:36]Br)=[C:28]([F:38])[CH:27]=1)[CH3:23]>CC(C)=O>[CH2:22]([O:24][C:25](=[O:39])[C:26]1[CH:31]=[CH:30][C:29]([O:32][CH2:33][CH2:34][CH2:35][CH2:36][N:9]2[CH2:8][CH2:7][N:6]([CH2:5][CH2:4][C:3]([CH3:13])([CH3:12])[CH3:2])[CH2:11][CH2:10]2)=[C:28]([F:38])[CH:27]=1)[CH3:23]参加物
6
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
1-(3,3-Dimethyl-butyl)-piperazine hydrochloride from Example E4 (874 mg, 3.7 mmol), potassium carbonate (2.5 g, 18.0 mmol) and potassium iodide (60 mg, 0.4 mmol) were added to a solution of 4-(4-bromo-butoxy)-3-fluoro-benzoic acid ethyl ester from Example E72.1 (1.4 g, 4.4 mmol) in acetone (35 ml) and the mixture was heated at reflux for 20 h. The solid was filtered off, washed with EtOAc and the filtrate was concentrated in vacuo. The residue was purified by flash chromatography on silica gel (eluant; EtOAc to 1% 35% ammonia:10% methanol:89% EtOAc) to yield the title compound (1.35 g, 90%).
後処理
- temperaturethe mixture was heated
- temperatureat reflux for 20 h
- filtrationThe solid was filtered off
- washwashed with EtOAc
- concentrationthe filtrate was concentrated in vacuo
- customThe residue was purified by flash chromatography on silica gel (eluant; EtOAc to 1% 35% ammonia:10% methanol:89% EtOAc)
出典と根拠
- ORDレコード
- ord-05444b003f1a483cb2fc8d6a8e8c3f2e
- 出典データセット
- uspto-grants-2012_06
- 特許番号
- US08202858B2
反応ノート
読み込み中…