反応式
[CH:1](=O)[C:2]1[CH:7]=[CH:6][N:5]=[CH:4][CH:3]=1.[CH3:9][N:10]1[C:15](=[O:16])[CH:14]=[C:13]([NH:17][N:18]=[CH:19][C:20]2[C:29]3[C:24](=[CH:25][CH:26]=[CH:27][CH:28]=3)[CH:23]=[CH:22][CH:21]=2)[NH:12][C:11]1=[O:30].N1CCCCC1.C(O)(=O)C>CN(C)C=O.C(O)(C)C>[CH3:9][N:10]1[C:15](=[O:16])[C:14]2=[C:1]([C:2]3[CH:7]=[CH:6][N:5]=[CH:4][CH:3]=3)[N:18]([CH2:19][C:20]3[C:29]4[C:24](=[CH:25][CH:26]=[CH:27][CH:28]=4)[CH:23]=[CH:22][CH:21]=3)[N:17]=[C:13]2[NH:12][C:11]1=[O:30]参加物
7
反応物 4
生成物 1
試薬・触媒・溶媒 2
反応条件
- 温度
- 120 °C
実験手順
Isonicotinaldehyde (0.87 g) was added to a solution of 1-naphthaldehyde (1-methyl-2,6-dioxo-1,2,3,6-tetrahydropyrimidin-4-yl)hydrazone (2.0 g) in dimethylformamide (66 ml) and isopropanol (16 ml). Piperidine (0.66 ml) was added followed by glacial acetic acid (0.08 ml). The solution was heated at 120° C. for 16 hours. Reaction cooled to room temperature, solids precipitated was filtered, and dried to give the subtitle compound (1.63 g). Mass: 383.93 (M+H).
後処理
- customReaction
- temperaturecooled to room temperature
- customsolids precipitated
- filtrationwas filtered
- customdried
出典と根拠
- ORDレコード
- ord-c54a94afde584aa088343351a0da5805
- 出典データセット
- uspto-grants-2007_10
- 特許番号
- US07285558B2
関連ノート
読み込み中…