Methyl Benzoate → 1-Phenyl-2-pyrazin-2-yl ethanone

HRID 401160

反応式

HRID 401160 の反応式
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

  1. stirringthe mixture was stirred at −78° C. for 30 minutes
  2. stirringthe mixture was stirred at this temperature for 3 hours
  3. customwas consumed
  4. additionthe reaction mixture was diluted with EtOAc
  5. washthe mixture was washed with water and brine
  6. concentrationconcentrated
  7. 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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