Trimethylsilylacetylene → Ethyl 2-ethynyl-4-methylthiazole-5-carboxylate
반응식
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]참가 물질
반응물 3
생성물 1
시약·촉매·용매 3
반응 조건
- 온도
- 40 °C
실험 절차
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).
후처리
- 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
출처 및 근거
- ORD 기록
- ord-b26cefe179654394ba6932596f8a53d7
- 출처 데이터셋
- uspto-grants-2012_09
- 특허 번호
- US08258160B2
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