反応式
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([O:21][CH2:22][C:23]([N:25]2[CH2:30][C@H:29]([CH3:31])[N:28]([CH2:32][C:33]3[CH:38]=[CH:37][C:36]([F:39])=[CH:35][CH:34]=3)[CH2:27][C@H:26]2[CH3:40])=[O:24])=[C:6]([S:8]([NH:11][C:12](=[O:20])[C:13]([O:16]C(=O)C)([CH3:15])[CH3:14])(=[O:10])=[O:9])[CH:7]=1.O.[OH-].[Li+]>O1CCCC1.CO.O>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([O:21][CH2:22][C:23]([N:25]2[CH2:30][C@H:29]([CH3:31])[N:28]([CH2:32][C:33]3[CH:34]=[CH:35][C:36]([F:39])=[CH:37][CH:38]=3)[CH2:27][C@H:26]2[CH3:40])=[O:24])=[C:6]([S:8]([NH:11][C:12](=[O:20])[C:13]([OH:16])([CH3:14])[CH3:15])(=[O:10])=[O:9])[CH:7]=1参加物
6
反応物 2
生成物 1
試薬・触媒・溶媒 3
実験手順
To a solution of acetic acid 2-(5-chloro-2-{2-[4-(4-fluoro-benzyl)-(2R,5S)-2,5-dimethyl-piperazin-1-yl]-2-oxo-ethoxy}-benzenesulfonylamino)-1,1-dimethyl-2-oxo-ethyl ester (0.14 g, 0.21 mmol) in tetrahydrofuran (2 mL), methanol (0.2 mL) and water (0.4 mL) was added lithium hydroxide monohydrate (0.020 g, 0.48 mmol). The resulting reaction mixture was stirred at ambient temperature overnight. Chromatography on silica gel of the reaction mixture provided the title compound (0.104 g, LRMS: 556.3).
後処理
- customThe resulting reaction mixture
出典と根拠
- ORDレコード
- ord-8e14bb657fa8415fa72446efe618afdc
- 出典データセット
- uspto-grants-2006_08
- 特許番号
- US07098212B2
関連ノート
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