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

HRID 924949

反応式

HRID 924949 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-c5a759b4d1374a8c838f7d6bfdea1b4a
出典データセット
uspto-grants-2016_03
特許番号
US09283229B2

関連ノート

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