Methyl iodide → Methyl 2-methyl-2H-indazole-3-carboxylate

HRID 1372738

反応式

HRID 1372738 の反応式
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]([C:10]([O:12][CH3:13])=[O:11])=[N:2]1.[H-].[Na+].[CH3:16]I.[Cl-].[NH4+]>CN(C=O)C>[CH3:16][N:2]1[C:3]([C:10]([O:12][CH3:13])=[O:11])=[C:4]2[C:9]([CH:8]=[CH:7][CH:6]=[CH:5]2)=[N:1]1

参加物

6

反応条件

温度
0 °C

実験手順

Methyl indazole-3-carboxylate (3.71 g, 21.1 mmol) was dissolved in DMF (40 ml). To the resulting solution was added sodium hydride (60% in oil, 1.01 g, 25.3 mmol) in portions under stirring at 0° C. The reaction mixture was stirred at the same temperature for 30 minutes. Methyl iodide (1.57 ml, 25.3 mmol) was added to the mixture. The resulting mixture was stirred at the same temperature for 30 minutes. A saturated aqueous solution of ammonium chloride was added and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and distilled under reduced pressure to remove the solvent. The residue was purified by chromatography on a silica gel column, whereby from n-hexane-ethyl acetate (3:1, v/v) eluate fractions, methyl 2-methylindazole-3-carboxylate (1.62 g, 26%) was obtained as a pale yellow solid.

後処理

  1. stirringThe reaction mixture was stirred at the same temperature for 30 minutes
  2. stirringThe resulting mixture was stirred at the same temperature for 30 minutes
  3. extractionthe mixture was extracted with ethyl acetate
  4. washThe extract was washed with saturated brine
  5. dry with materialdried over anhydrous magnesium sulfate
  6. distillationdistilled under reduced pressure
  7. customto remove the solvent
  8. customThe residue was purified by chromatography on a silica gel column, whereby from n-hexane-ethyl acetate (3:1

出典と根拠

ORDレコード
ord-f95a75addd494d208704cd6c559d5320
出典データセット
uspto-grants-2007_01
特許番号
US07157487B2

関連ノート

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