Trimethylsilylacetylene → Ethyl 2-ethynyl-4-methylthiazole-5-carboxylate
反応式
Br[C:2]1[S:3][C:4]([C:8]([O:10][CH2:11][CH3:12])=[O:9])=[C:5]([CH3:7])[N:6]=1.[CH:13](N(CC)C(C)C)(C)[CH3:14].C[Si](C#C)(C)C>C1(C)C=CC=CC=1.[Cu]I.Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1>[C:13]([C:2]1[S:3][C:4]([C:8]([O:10][CH2:11][CH3:12])=[O:9])=[C:5]([CH3:7])[N:6]=1)#[CH:14]参加物
反応物 3
生成物 1
試薬・触媒・溶媒 3
反応条件
- 温度
- 40 °C
実験手順
To a degassed solution of ethyl 2-bromo-4-methylthiazole-5-carboxylate (0.50 g, 2.00 mmol) in toluene (10 mL) was added N,N-diisopropylethylamine (0.5 mL, 3.0 mmol), copper(I) iodide (0.01 g, 0.06 mmol), trimethylsilylacetylene (0.05 mL, 3.70 mmol) and bis(triphenylphosphine)palladium(II) dichloride (0.05 g, 0.06 mmol). The reaction mixture was heated at 40° C. under nitrogen for 5 hours, cooled to ambient temperature and concentrated in vacuo. The residue was dissolved in methanol (10 mL) and 10% lithium hydroxide solution (0.5 mL). The reaction mixture was stirred at ambient temperature for 10 minutes and extracted with dichloromethane. The organic layer was washed with water, brine, dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated in vacuo, and the residue was purified by column chromatography to afford the title compound as a white solid (0.31 g, 77%): MS (ES+) m/z 196.2 (M+1).
後処理
- temperaturecooled to ambient temperature
- concentrationconcentrated in vacuo
- dissolutionThe residue was dissolved in methanol (10 mL)
- extractionextracted with dichloromethane
- washThe organic layer was washed with water, brine
- dry with materialdried over anhydrous sodium sulfate
- filtrationfiltered
- concentrationThe filtrate was concentrated in vacuo
- customthe residue was purified by column chromatography
出典と根拠
- ORDレコード
- ord-b26cefe179654394ba6932596f8a53d7
- 出典データセット
- uspto-grants-2012_09
- 特許番号
- US08258160B2
反応ノート
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