Hydrochloric Acid → N-(4-Formyl-2-pyrimidinyl)acetamide
反応式
C[O-].[Na+].C(O[O:8][CH:9](OC)[C:10]1[CH:15]=[CH:14][N:13]=[C:12]([NH:16][C:17](=[O:19])[CH3:18])[N:11]=1)(=O)C.Cl>CO>[C:17]([NH:16][C:12]1[N:11]=[C:10]([CH:9]=[O:8])[CH:15]=[CH:14][N:13]=1)(=[O:19])[CH3:18]参加物
5
実験手順
Sodium methoxide (0.056 g, 1.0 mmol) was added to a solution of 2-acetamidopyrimidine-4-carboxaldehyde monomethyl monoacetoxy acetal (5.0 g, 21 mmol) in MeOH (25 mL) at ambient temperature. After stirring at this temperature for 3 h, the reaction mixture was neutralized by addition of 3N HCl. The resulting solution was concentrated and the residue was treated with CH2Cl2. Remaining solids were removed by filtration and the solvent was evaporated to afford the title compound as a yellow solid; yield 3.2 g (92%).
後処理
- concentrationThe resulting solution was concentrated
- additionthe residue was treated with CH2Cl2
- customwere removed by filtration
- customthe solvent was evaporated
出典と根拠
- ORDレコード
- ord-831c788ac561405793c64b07b08f3f3c
- 出典データセット
- uspto-grants-1997_01
- 特許番号
- US05593992
反応ノート
読み込み中…