Ammonia → 6-Amino-4-chloro-2-isopropylamino-5-pyrimidinecarbonitrile
反応式
[NH3:1].[Cl:2][C:3]1[C:8]([C:9]#[N:10])=[C:7](Cl)[N:6]=[C:5](NCC)[N:4]=1.[CH:15]([NH2:18])([CH3:17])[CH3:16]>>[NH2:1][C:7]1[N:6]=[C:5]([NH:18][CH:15]([CH3:17])[CH3:16])[N:4]=[C:3]([Cl:2])[C:8]=1[C:9]#[N:10]参加物
4
実験手順
This compound was prepared in the manner of Example XVII, substituting 4,6-dichloro-2-isopropylamino-5-pyrimidinecarbonitrile and aqueous ammonia for 4,6-dichloro-2-ethylamino-5-pyrimidinecarbonitrile and isopropylamine. The reaction product was recrystallized from benzene to give 6-amino-4-chloro-2-isopropylamino-5-pyrimidinecarbonitrile; mp, 162°-165°.
後処理
- customThis compound was prepared in the manner of Example XVII
- customThe reaction product was recrystallized from benzene
出典と根拠
- ORDレコード
- ord-841a6010216a4ab38c2501ebd055c763
- 出典データセット
- uspto-grants-1983_02
- 特許番号
- USRE031136
反応ノート
読み込み中…