[(Aminocarbonyl)hydrazono](phenyl)acetaldehyde → 6-Phenyl-1,2,4-triazin-3(2H)-one
反応式
[NH2:1][C:2]([NH:4][N:5]=[C:6]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)[CH:7]=O)=[O:3]>C(O)(=O)C>[C:9]1([C:6]2[CH:7]=[N:1][C:2](=[O:3])[NH:4][N:5]=2)[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1参加物
3
実験手順
[(Aminocarbonyl)hydrazono](phenyl)acetaldehyde (3.00 g, 0.0157 mol) in acetic acid (15.0 mL) was heated at 130° C. for 6 h. After cooling, the solvent was removed under reduced pressure. The residue was triturated with ether, filtered, washed with ether, and dried under high vacuum to give the desired product (2.45 g, 90.1%). Analytical LCMS: (M+H)+=174.0.
後処理
- temperatureAfter cooling
- customthe solvent was removed under reduced pressure
- customThe residue was triturated with ether
- filtrationfiltered
- washwashed with ether
- customdried under high vacuum
出典と根拠
- ORDレコード
- ord-c4086d089c624ad5801abddf5ee6eb32
- 出典データセット
- uspto-grants-2010_03
- 特許番号
- US07683060B2
反応ノート
読み込み中…