反応式
C(=O)([O-])[O-].[K+].[K+].[CH3:7][O:8][C:9](=[O:39])[NH:10][CH:11]([C:15]([N:17]1[CH2:21][CH2:20][CH2:19][CH:18]1[C:22]1[NH:23][C:24]([C:27]2[CH:32]=[CH:31][C:30]([C:33]#[C:34][Si](C)(C)C)=[CH:29][CH:28]=2)=[CH:25][N:26]=1)=[O:16])[CH:12]([CH3:14])[CH3:13]>CO>[CH3:7][O:8][C:9](=[O:39])[NH:10][CH:11]([C:15]([N:17]1[CH2:21][CH2:20][CH2:19][CH:18]1[C:22]1[NH:23][C:24]([C:27]2[CH:32]=[CH:31][C:30]([C:33]#[CH:34])=[CH:29][CH:28]=2)=[CH:25][N:26]=1)=[O:16])[CH:12]([CH3:14])[CH3:13]参加物
4
反応物 2
生成物 1
試薬・触媒・溶媒 1
実験手順
Potassium carbonate (192 mg) was added to (2-Methyl-1-{2-[5-(4-trimethylsilanylethynyl-phenyl)-1H-imidazol-2-yl]-pyrrolidine-1-carbonyl}-propyl)-carbamic acid methyl ester (324 mg) in 7 mL MeOH solution. The reaction was stirred at room temperature overnight. The reaction mixture was concentrated down and purified by flash column chromatography (silica gel, 20 to 100% ethyl acetate/hexane) to give (1-{2-[5-(4-Ethynyl-phenyl)-1H-imidazol-2-yl]-pyrrolidine-1-carbonyl}-2-methyl-propyl)-carbamic acid methyl ester (234 mg).
後処理
- concentrationThe reaction mixture was concentrated down
- custompurified by flash column chromatography (silica gel, 20 to 100% ethyl acetate/hexane)
出典と根拠
- ORDレコード
- ord-4078268673904da881fdf1973b6e2a9c
- 出典データセット
- uspto-grants-2014_09
- 特許番号
- US08822430B2
関連ノート
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