反応式
[CH:1]([C:3]1[NH:7][C:6]([C:8]([O:10][CH2:11][CH3:12])=[O:9])=[C:5]([CH3:13])[CH:4]=1)=O.[C:14]([O:20][CH2:21][CH3:22])(=[O:19])[CH2:15]C([O-])=O.N1CCCCC1>N1C=CC=CC=1>[CH2:21]([O:20][C:14](/[CH:15]=[CH:1]/[C:3]1[NH:7][C:6]([C:8]([O:10][CH2:11][CH3:12])=[O:9])=[C:5]([CH3:13])[CH:4]=1)=[O:19])[CH3:22]参加物
5
反応条件
- 温度
- 100 °C
実験手順
Ethyl 5-formyl-3-methyl-1H-pyrrole-2-carboxylate 470 mg, monoethyl malonate 378 mg, piperidine 0.05 mL and pyridine 6 mL were mixed and stirred at 100° C. for 38 hours. Ice water was added to the reaction liquid and the precipitate was recovered by filtration. The precipitate was washed with water and dried in flowing air under heating to provide 311 mg of the title compound.
後処理
- filtrationthe precipitate was recovered by filtration
- washThe precipitate was washed with water
- customdried
- temperatureunder heating
出典と根拠
- ORDレコード
- ord-03e6a0fb06e24cdfbdfa2e6c1dfb14ae
- 出典データセット
- uspto-grants-2012_10
- 特許番号
- US08299080B2
関連ノート
読み込み中…