反応式
C[O:2][C:3]1[N:8]=[C:7]([O:9]C)[C:6]([C:11]2[C:12]([C:17]#[N:18])=[N:13][CH:14]=[CH:15][CH:16]=2)=[CH:5][N:4]=1.[ClH:19]>O1CCOCC1>[ClH:19].[O:2]=[C:3]1[NH:8][C:7](=[O:9])[C:6]([C:11]2[C:12]([C:17]#[N:18])=[N:13][CH:14]=[CH:15][CH:16]=2)=[CH:5][NH:4]1参加物
4
実験手順
3-(2,4-Dimethoxy-pyrimidin-5-yl)-pyridine-2-carbonitrile (Prep102, 1 g, 4.13 mmol) was dissolved in a solution of 4N HCl in dioxane (20 ml). The mixture was refluxed for 45 minutes. The solvent was removed under vacuum to give 1 g of the title compound (97% yield).
後処理
- temperatureThe mixture was refluxed for 45 minutes
- customThe solvent was removed under vacuum
出典と根拠
- ORDレコード
- ord-60811416b8df4b4dbe46a3d4a9ede2b1
- 出典データセット
- uspto-grants-2010_06
- 特許番号
- US07727988B2
関連ノート
読み込み中…