Methyl iodide → 1-Methyl-1H-indole-5-carboxylic acid

HRID 1883207

反応式

HRID 1883207 の反応式
N1C2C(=CC(C(O)=O)=CC=2)C=C1.[H-].[Na+].IC.[CH3:17][N:18]1[C:26]2[C:21](=[CH:22][C:23]([C:27]([O:29]C)=[O:28])=[CH:24][CH:25]=2)[CH:20]=[CH:19]1.[OH-].[Na+]>CN(C=O)C.C1COCC1.CO.O>[CH3:17][N:18]1[C:26]2[C:21](=[CH:22][C:23]([C:27]([OH:29])=[O:28])=[CH:24][CH:25]=2)[CH:20]=[CH:19]1

参加物

10

反応条件

温度
0 °C

実験手順

Under nitrogen atmosphere, a solution of indole-5-carboxylic acid (1.05 g) in DMF (40 mL) was cooled to 0° C., and thereto was added NaH (544 mg, 60%), and the mixture was stirred at the same temperature for 10 minutes, and stirred at room temperature for 30 minutes. The mixture was cooled to 0° C., and thereto was added iodomethane (3.68 g), and the mixture was stirred at room temperature for 48 hours. Water was added to the mixture, and the mixture was extracted three times with ethyl acetate-toluene, and dried over MgSO4. The solvent was evaporated under reduced pressure to give a crude methyl 1-methylindole-5-carboxylate. To a solution of the crude methyl 1-methylindole-5-carboxylate in THF (50 mL)-MeOH (50 mL) was added a 6N NaOH solution (5.4 mL), and the mixture was stirred at room temperature for 144 hours. The solvent was evaporated under reduced pressure. The residue was washed with ethyl acetate, and thereto was added a 6N aqueous hydrochloric acid solution to adjust the pH value thereof to pH=5-6. The mixture was extracted twice with ethyl acetate, and dried over MgSO4. The solvent was evaporated under reduced pressure to give 1-methyl-1H-indol-5-carboxylic acid (1.08 g, 96%).

後処理

  1. stirringstirred at room temperature for 30 minutes
  2. stirringthe mixture was stirred at room temperature for 48 hours
  3. extractionthe mixture was extracted three times with ethyl acetate-toluene
  4. dry with materialdried over MgSO4
  5. customThe solvent was evaporated under reduced pressure
  6. customto give a crude methyl 1-methylindole-5-carboxylate
  7. stirringthe mixture was stirred at room temperature for 144 hours
  8. customThe solvent was evaporated under reduced pressure
  9. washThe residue was washed with ethyl acetate
  10. additionwas added a 6N aqueous hydrochloric acid solution
  11. extractionThe mixture was extracted twice with ethyl acetate
  12. dry with materialdried over MgSO4
  13. customThe solvent was evaporated under reduced pressure

出典と根拠

ORDレコード
ord-6b914eadaa3c4d2ba35010d8d655f09f
出典データセット
uspto-grants-2004_07
特許番号
US06759429B2

関連ノート

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