Methylamine → N-methyl-1H-indole-2-carboxamide
反応式
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=[C:2]1[C:10]([O:12]CC)=O.[CH3:15][NH2:16]>>[CH3:15][NH:16][C:10]([C:2]1[NH:1][C:9]2[C:4]([CH:3]=1)=[CH:5][CH:6]=[CH:7][CH:8]=2)=[O:12]参加物
3
実験手順
A suspension of ethyl indole-2-carboxylate (25.30 g, 133.7 mmole) in 40% aqueous CH3NH2 (400 mL) was stirred at RT. The flask was tightly stoppered to keep the material inside the flask. As the reaction proceeded the product began to precipitate. The reaction was stirred at RT for 3 days, then was concentrated to remove approximately 200 mL of the solvent. The remaining residue was diluted with H2O (500 mL), and the solid was collected by suction filtration and washed with H2O. Drying under high vacuum left the title compound (21.50 g, 92%) as a light yellow solid: MS (ES) m/e 175 (M+H)+.
後処理
- customto precipitate
- stirringThe reaction was stirred at RT for 3 days
- concentrationwas concentrated
- customto remove approximately 200 mL of the solvent
- additionThe remaining residue was diluted with H2O (500 mL)
- filtrationthe solid was collected by suction filtration
- washwashed with H2O
- customDrying under high vacuum
- waitleft the title compound (21.50 g, 92%) as a light yellow solid
出典と根拠
- ORDレコード
- ord-a3dad9a06c5147259303288e2d02c0e3
- 出典データセット
- uspto-grants-2009_07
- 特許番号
- US07557125B2
反応ノート
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