反応式
CS[C:3]1[N:8]=[C:7]([OH:9])[C:6]([C:10]([O:12][CH2:13][CH3:14])=[O:11])=[CH:5][N:4]=1.C(O)(=O)C.[CH2:19]([NH2:22])[CH2:20][CH3:21]>O>[CH2:19]([NH:22][C:3]1[N:8]=[C:7]([OH:9])[C:6]([C:10]([O:12][CH2:13][CH3:14])=[O:11])=[CH:5][N:4]=1)[CH2:20][CH3:21]参加物
4
実験手順
2-Methylthio-5-ethoxycarbonyl-4-hydroxypyrimidine (2 mmol, 428 mg) was heated on an oil bath at 160° C. with n-propylamine acetate (1 ml) for 1 hour. The semi solid was cooled and then treated with 50 ml boiling water, and the solid product was filtered off (yield 400 mg, 88%)
後処理
- temperatureThe semi solid was cooled
- additiontreated with 50 ml
- filtrationthe solid product was filtered off (yield 400 mg, 88%)
出典と根拠
- ORDレコード
- ord-29a8e092abdd40efa21bc881d67aaf27
- 出典データセット
- uspto-grants-1984_05
- 特許番号
- US04447422
関連ノート
読み込み中…