Water → HCID 12795550、化合物
反応式
[Cl:1][C:2]1[CH:3]=[N:4][C:5](=[O:8])[NH:6][CH:7]=1.[C:9]([NH:17][C:18]1[CH:23]=[CH:22][C:21]([C:24](=[O:27])[CH2:25]Br)=[CH:20][CH:19]=1)(=[O:16])[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1.O>C(N(CC)CC)C.CN(C)C=O>[C:9]([NH:17][C:18]1[CH:19]=[CH:20][C:21]([C:24](=[O:27])[CH2:25][N:4]2[CH:3]=[C:2]([Cl:1])[CH:7]=[N:6][C:5]2=[O:8])=[CH:22][CH:23]=1)(=[O:16])[C:10]1[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=1参加物
6
実験手順
A suspension of 5-chloropyrimidin-2-one (338 mg) and 4'-benzamido-2-bromoacetophenone (766 mg) in triethylamine (1 ml) and dimethylformamide (10 ml) was stirred at ambient temperature, giving a solution, quickly followed by formation of a precipitate. After 45 mins, water (100 ml) was added to the suspension. The collected solid was crystallised from glacial acetic acid to give the title pyrimidinone (439 mg,); m.p. 290°-303°; λmaxEtOH 226 nm (ε 16230), 302.5 nm (ε 20370).
後処理
- customgiving a solution
- customThe collected solid was crystallised from glacial acetic acid
出典と根拠
- ORDレコード
- ord-19343eca45de4de2b7471de3fe432f1b
- 出典データセット
- uspto-grants-1987_01
- 特許番号
- US04636509
反応ノート
読み込み中…