Malonic Acid → (E)-3-(6-Acetamidopyridin-3-YL)acrylic acid
反応式
[C:1]([NH:4][C:5]1[CH:10]=[CH:9][C:8]([CH:11]=O)=[CH:7][N:6]=1)(=[O:3])[CH3:2].C(O)(=O)[CH2:14][C:15]([OH:17])=[O:16]>N1C=CC=CC=1.C(O)C>[C:1]([NH:4][C:5]1[N:6]=[CH:7][C:8](/[CH:11]=[CH:14]/[C:15]([OH:17])=[O:16])=[CH:9][CH:10]=1)(=[O:3])[CH3:2]参加物
5
実験手順
A mixture of 2-acetylamino-5-formylpyridine (241 mg) and malonic acid (168 mg) in pyridine (0.12 ml) and ethanol (0.36 ml) was refluxed for 2 hours. After cooling the mixture, the precipitate was collected by filtration, and washed with ethyl acetate to give (E)-3-(6-acetylamino-3-pyridyl)acrylic acid (248 mg) as a colorless powder.
後処理
- temperaturewas refluxed for 2 hours
- temperatureAfter cooling the mixture
- filtrationthe precipitate was collected by filtration
- washwashed with ethyl acetate
出典と根拠
- ORDレコード
- ord-7733673bba7a45f79c08321c871f141a
- 出典データセット
- uspto-grants-1996_10
- 特許番号
- US05563162
反応ノート
読み込み中…