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2-Pyrazinecarboxylic acid → N-Methoxy-N-methylpyrazine-2-carboxamide

HRID 8211
ノート
印刷プレビュー

反応式

HRID 8211 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 10472-Pyrazinecarboxylic acidHCID 6228DimethylformamideHCID 8471TriethylamineHCID 65578Oxalyl chlorideHCID 81138Methanamine, N-methoxy-, hydrochloride (1:1)

生成物 1

HCID 22613131N-Methoxy-N-methylpyrazine-2-carboxamide

試薬・触媒・溶媒 1

HCID 6344
Dichloromethane
溶媒
2 回

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-88a28dff53a6456da92966bba8830b33
出典データセット
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07087626B2

反応ノート

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