反応式
[F:1][C:2]([F:7])([F:6])[C:3]([NH2:5])=[NH:4].[CH2:8]([O:10][C:11](=[O:18])[C:12](=O)[CH2:13][C:14](=O)[CH3:15])[CH3:9].Cl.C([O-])(O)=O.[Na+]>C(O)C>[CH2:8]([O:10][C:11]([C:12]1[CH:13]=[C:14]([CH3:15])[N:5]=[C:3]([C:2]([F:7])([F:6])[F:1])[N:4]=1)=[O:18])[CH3:9]参加物
反応条件
- 温度
- 2.5 °C
実験手順
2.241 g (20 mmol) of 2,2,2-trifluoro-acetamidine were dissolved in 80 ml ethanol and treated with 3.163 g (20 mmol) of 2,4-dioxo-pentanoic acid ethyl ester. The resulting solution was cooled to 0-5° C. and treated with 120 ml of HCl-saturated ethanol. The reaction mixture was allowed to warm-up to RT and stirred for additional 3 hours. The mixture was then added dropwise under cooling to 800 ml saturated NaHCO3 solution. The resulting mixture was then extracted twice with 300 ml DCM and the combined organic phases were dried over magnesium sulfate, filtered and concentrated in vacuo to yield 3.1 g of a yellow oil. This residue was then purified by silicagel chromatography (eluent:heptane/ethyl acetate 100:0 to 30:70) leading to a colorless oil which crystallized spontaneously, leading to 1.3 g of 6-methyl-2-trifluoromethyl-pyrimidine-4-carboxylic acid ethyl ester.
後処理
- temperatureto warm-up to RT
- additionThe mixture was then added dropwise
- extractionThe resulting mixture was then extracted twice with 300 ml DCM
- dry with materialthe combined organic phases were dried over magnesium sulfate
- filtrationfiltered
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-55d22c8d6fd644f08315a4bb10965fba
- 出典データセット
- uspto-grants-2010_06
- 特許番号
- US07745477B2
関連ノート
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