反応式
C(Cl)(=O)C(Cl)=O.[CH3:7][N:8]1[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH:10]=[C:9]1[C:17]([OH:19])=O.[CH3:20][C:21]1([CH3:35])[C:25]([CH3:27])([CH3:26])[O:24][B:23]([C:28]2[CH:34]=[CH:33][C:31]([NH2:32])=[CH:30][CH:29]=2)[O:22]1.C(N(C(C)C)CC)(C)C>CN(C)C=O.ClCCl>[CH3:7][N:8]1[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH:10]=[C:9]1[C:17]([NH:32][C:31]1[CH:30]=[CH:29][C:28]([B:23]2[O:24][C:25]([CH3:27])([CH3:26])[C:21]([CH3:35])([CH3:20])[O:22]2)=[CH:34][CH:33]=1)=[O:19]参加物
7
反応物 4
生成物 1
試薬・触媒・溶媒 2
実験手順
A mixture of oxalyl chloride (0.35 mL) and dimethylformamide (1 drop) was added to a solution of 1-methyl-1H-2-indolecarboxylic acid (440 mg, 2.51 mmol) in dichloromethane (10 mL). After one hour the mixture was evaporated, dissolved in dichloromethane (10 mL), and added to a mixture of 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline (500 mg, 2.28 mmol) and diisopropylethylamine (0.35 mL) in dichloromethane (10 mL). After 16 hours the mixture was washed with water (10 mL), dried (MgSO4), filtered, concentrated, and purified by flash column chromatography to provide the desired product (600 mg, 1.60 mmol) after lyophilization: MS m/e 377.4 (M+H)+.
後処理
- customAfter one hour the mixture was evaporated
- dissolutiondissolved in dichloromethane (10 mL)
- washAfter 16 hours the mixture was washed with water (10 mL)
- dry with materialdried (MgSO4)
- filtrationfiltered
- concentrationconcentrated
- custompurified by flash column chromatography
出典と根拠
- ORDレコード
- ord-00dd9d9dddeb4439adc214beea6eb3c3
- 出典データセット
- uspto-grants-2010_06
- 特許番号
- US07737160B2
関連ノート
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