Methylamine → 6-AMINO-1-BENZYL-5-METHYLAMINOURACIL
反応式
[NH2:1][C:2]1[N:7]([CH2:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[C:6](=[O:15])[NH:5][C:4](=[O:16])[C:3]=1Br.[CH3:18][NH2:19]>>[NH2:1][C:2]1[N:7]([CH2:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[C:6](=[O:15])[NH:5][C:4](=[O:16])[C:3]=1[NH:19][CH3:18]参加物
3
反応条件
- 温度
- 5 °C
実験手順
6-Amino-1-benzyl-5-bromouracil (134 g) was stirred with 40% aqueous methylamine solution (750 ml) for 24 hours. After cooling to 5° C., the precipitate was filtered and dried under suction to provide 6-amino-1-benzyl-5-methylaminouracil (55 g).
後処理
- filtrationthe precipitate was filtered
- customdried under suction
出典と根拠
- ORDレコード
- ord-03cb572469a64cfe963762ddab5d3eb1
- 出典データセット
- uspto-grants-2005_04
- 特許番号
- US06878715B1
反応ノート
読み込み中…