Ammonia → 2-(2-Propoxy-5-sulphamoylphenyl)purin-6-one
反応式
[CH2:1]([O:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[C:11]1[N:19]=[C:18]2[C:14](=[N:15][CH:16]=[N:17]2)[C:13](=[O:20])[N:12]=1)[CH2:2][CH3:3].Cl[S:22]([OH:25])(=O)=[O:23].[NH3:26]>>[CH2:1]([O:4][C:5]1[CH:10]=[CH:9][C:8]([S:22](=[O:25])(=[O:23])[NH2:26])=[CH:7][C:6]=1[C:11]1[N:19]=[C:18]2[C:14](=[N:15][CH:16]=[N:17]2)[C:13](=[O:20])[N:12]=1)[CH2:2][CH3:3]参加物
4
実験手順
In a similar manner to Example 18 reaction of 2-(2-propoxyphenyl)purin-6-one (0.95 g) with chlorosulphonic acid (4.5 ml), followed by reaction with saturated methanolic ammonia (50 ml), yielded a crude product (0.92 g) which was recrystallised from aqueous ethanol and then from dimethylformamide to yield the pure title compound, 0.59 g, m.p. 276°-278° C.
後処理
- customyielded a crude product (0.92 g) which
- customwas recrystallised from aqueous ethanol
出典と根拠
- ORDレコード
- ord-ce6cd8da623e47bc9ef9f2b24cdda953
- 出典データセット
- uspto-grants-1991_12
- 特許番号
- US05073559
反応ノート
読み込み中…