反応式
[Cl:1][C:2]1[CH:7]=[C:6]([NH:8][C:9](=[O:11])[CH3:10])[CH:5]=[CH:4][N:3]=1.[OH-].[K+].[CH3:14]I>CC(C)=O>[Cl:1][C:2]1[CH:7]=[C:6]([N:8]([CH3:14])[C:9](=[O:11])[CH3:10])[CH:5]=[CH:4][N:3]=1参加物
5
実験手順
A mixture of 10 g (59 mmol) N-(2-chloropyridin-4-yl)acetamide (commercially available), 9.8 g (17.6 mmol) pulverized KOH and 4.1 ml (6.4 mmol) methyl iodide in 60 ml acetone was stirred at room temperature for 2 h. After evaporation of all volatiles the residue was taken up in water and extracted with ethyl acetate. The combined organic layers were dried with MgSO4 and evaporated to yield 7.1 g (66%) of the title compound as off-white solid. MS: (m/e): 345.2 (MH+).
後処理
- customAfter evaporation of all volatiles the residue
- extractionextracted with ethyl acetate
- dry with materialThe combined organic layers were dried with MgSO4
- customevaporated
出典と根拠
- ORDレコード
- ord-eefef0b6d44841ecbdb586d02b318f21
- 出典データセット
- uspto-grants-2009_11
- 特許番号
- US07612076B2
関連ノート
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