反応式
C(NC(C)C)(C)C.[Li]CCCC.[CH3:13][C:14]1[CH:19]=[N:18][CH:17]=[CH:16][N:15]=1.[C:20](OC)(=[O:27])[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1>C1COCC1>[C:21]1([C:20](=[O:27])[CH2:13][C:14]2[CH:19]=[N:18][CH:17]=[CH:16][N:15]=2)[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1参加物
6
実験手順
To a mixture of diisopropyl-amine (1.29 g, 12.7 mmol) in anhydrous THF (10 mL) was added n-BuLi (2.5 M/L in hexane, 4.7 mL, 11.7 mmol) at −78° C., after being stirred for 30 minutes, a solution of 2-methylpyrazine (1 g, 10.6 mmol) in THF (5 mL) was added, and the mixture was stirred at −78° C. for 30 minutes, a solution of methyl benzoate (1.4 g, 10.6 mmol) in THF (5 mL) was added, and the mixture was stirred at this temperature for 3 hours. When TLC indicated that the starting material was consumed, the reaction mixture was diluted with EtOAc, and the mixture was washed with water and brine, and concentrated. The residue was purified by column chromatography (PE:EtOAc=30:1) to give Intermediate 26 (700 mg, yield 33.3%).
後処理
- stirringthe mixture was stirred at −78° C. for 30 minutes
- stirringthe mixture was stirred at this temperature for 3 hours
- customwas consumed
- additionthe reaction mixture was diluted with EtOAc
- washthe mixture was washed with water and brine
- concentrationconcentrated
- customThe residue was purified by column chromatography (PE:EtOAc=30:1)
出典と根拠
- ORDレコード
- ord-26abdd557f50405497b6d8bb48062aea
- 出典データセット
- uspto-grants-2014_06
- 特許番号
- US08741915B2
関連ノート
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