Ethanol → 4-Ethoxy-6-ethylamino-2-isopropylamino-5-pyrimidinecarbonitrile
反応式
[Na].Cl[C:3]1[C:8]([C:9]#[N:10])=[C:7]([NH:11][CH2:12][CH3:13])[N:6]=[C:5]([NH:14][C:15]([C:18]#N)([CH3:17])C)[N:4]=1.[CH2:20]([OH:22])[CH3:21]>CO>[CH2:20]([O:22][C:3]1[C:8]([C:9]#[N:10])=[C:7]([NH:11][CH2:12][CH3:13])[N:6]=[C:5]([NH:14][CH:15]([CH3:17])[CH3:18])[N:4]=1)[CH3:21]参加物
5
実験手順
This compound was prepared in the manner of Example XXXIII, substituting 4-chloro-6-ethylamino-2-isopropylamino-5-pyrimidinecarbonitrile and a solution of sodium in ethanol for 4-chloro-2-(1-cyano-1-methylethylamino)-6-ethylamino-5-pyrimidinecarbonitrile and a solution of sodium in methanol. The reaction product was recrystallized from petroleum ether to give 4-ethoxy-6-ethylamino-2-isopropylamino-5-pyrimidinecarbonitrile; mp, 98°-99°.
後処理
- customThis compound was prepared in the manner of Example XXXIII
- customThe reaction product was recrystallized from petroleum ether
出典と根拠
- ORDレコード
- ord-145fe1dce161482889350fbb0c6124f6
- 出典データセット
- uspto-grants-1978_05
- 特許番号
- US04092150
反応ノート
読み込み中…