2-甲酸吡嗪 → N-甲氧基-N-甲基-吡嗪-2-甲酰胺

HRID 8211

反应方程式

HRID 8211 反应方程式
[N:1]1[CH:6]=[CH:5][N:4]=[CH:3][C:2]=1[C:7]([OH:9])=O.C(Cl)(=O)C(Cl)=O.CN(C)C=O.Cl.[CH3:22][NH:23][O:24][CH3:25].C(N(CC)CC)C>C(Cl)Cl>[CH3:25][O:24][N:23]([CH3:22])[C:7]([C:2]1[CH:3]=[N:4][CH:5]=[CH:6][N:1]=1)=[O:9]

参与物

7

实验过程

To a solution of pyrazine-2-carboxylic acid (2.0 g, 16.1 mmol) in methylene chloride (54 mL) at 0° C. is added oxalyl chloride (7.1 mL, 80.6 mmol) and N,N-dimethylformamide (0.12 mL, 1.6 mmol). The cooling bath is removed after 10 min and the reaction mixture stirred 18 h at room temperature. The reaction mixture is concentrated in vacuo. The residual oil is dissolved in methylene chloride (54 mL) and treated with N,O-dimethylhydroxylamine hydrochloride (2.36 g, 24.15 mmol) and triethylamine (11.2 mL, 80.6 mmol). The reaction mixture is stirred for 3 h at room temperature and diluted with methylene chloride. The resulting mixture is washed with water (50 mL), saturated aqueous bicarbonate (50 mL), and brine (100 mL), and concentrated in vacuo to yield the title compound, 2.35 g (88%), as a brown oil.

后处理

  1. customThe cooling bath is removed after 10 min
  2. concentrationThe reaction mixture is concentrated in vacuo
  3. dissolutionThe residual oil is dissolved in methylene chloride (54 mL)
  4. stirringThe reaction mixture is stirred for 3 h at room temperature
  5. washThe resulting mixture is washed with water (50 mL), saturated aqueous bicarbonate (50 mL), and brine (100 mL)
  6. concentrationconcentrated in vacuo

来源与证据

ORD记录
ord-88a28dff53a6456da92966bba8830b33
来源数据集
uspto-grants-2006_08
专利号
US07087626B2

关联笔记

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