反応式
[C:1]([C:4]1[CH:5]=[C:6]([NH:10][C:11]2[CH:16]=[C:15]([CH3:17])[N:14]=[C:13]([NH2:18])[N:12]=2)[CH:7]=[CH:8][CH:9]=1)(=[O:3])[CH3:2].[CH3:19][I:20]>CC(C)=O>[I-:20].[C:1]([C:4]1[CH:5]=[C:6]([NH:10][C:11]2[CH:16]=[C:15]([CH3:17])[N+:14]([CH3:19])=[C:13]([NH2:18])[N:12]=2)[CH:7]=[CH:8][CH:9]=1)(=[O:3])[CH3:2]参加物
4
実験手順
4-(3-acetylphenyl)amino-2-amino-6-methylpyrimidine, Compound No. 15, (0.968 g) was suspended in acetone (5 mL) containing methyl iodide (2 mL) was heated at reflux for 48 hr. Filtration after cooling gave 0.657 g of 4-(3-acetylphenyl)amino-2-amino-1,6-dimethylpyrimidinium iodide as a white powder, mp 238°-40° C.
後処理
- temperaturewas heated
- temperatureat reflux for 48 hr
- filtrationFiltration
- temperatureafter cooling
出典と根拠
- ORDレコード
- ord-053a3b933b364923bf2f91b0c96e42aa
- 出典データセット
- uspto-grants-1996_11
- 特許番号
- US05574040
関連ノート
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