반응식
[CH3:1][CH:2]1[CH2:6][CH2:5][O:4][C:3]1=O.S(Cl)(Cl)=O.[CH2:12]([N:19]1[CH2:24][CH2:23][N:22]([NH2:25])[CH2:21][CH2:20]1)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.[H-].[Na+]>C1COCC1.[Cl-].[Zn+2].[Cl-]>[CH2:12]([N:19]1[CH2:20][CH2:21][N:22]([N:25]2[CH2:5][CH2:6][CH:2]([CH3:1])[C:3]2=[O:4])[CH2:23][CH2:24]1)[C:13]1[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=1참가 물질
반응 조건
- 온도
- 80 °C
실험 절차
A mixture of 3-methyldihydrofuran-2(3H)-one (2.0 g), thionyl chloride (1.5 ml) and zinc chloride (10 mg) was stirred at 80° C. for 15 hours. The mixture was cooled to room temperature, and the reaction mixture was added dropwise to a solution of 4-benzylpiperazin-1-amine (3.8 g) in THF (50 mL) at 0° C., followed by stirring at 0° C. for 2 hours. Sodium hydride (60% in oil; 2.4 g) was added thereto and the mixture was stirred at room temperature for 15 hours. Ice was added thereto, and then the reaction mixture was concentrated under reduced pressure. The residue was diluted with water, and extracted with dichloromethane. The extract was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The residue obtained was purified by basic silica gel column chromatography (ethyl acetate/hexane=1/5) to obtain the title compound (2.0 g, 37%) as a yellow oil.
후처리
- temperatureThe mixture was cooled to room temperature
- stirringby stirring at 0° C. for 2 hours
- stirringthe mixture was stirred at room temperature for 15 hours
- additionIce was added
- concentrationthe reaction mixture was concentrated under reduced pressure
- additionThe residue was diluted with water
- extractionextracted with dichloromethane
- dry with materialThe extract was dried over anhydrous sodium sulfate
- distillationthe solvent was distilled off under reduced pressure
- customThe residue obtained
- customwas purified by basic silica gel column chromatography (ethyl acetate/hexane=1/5)
출처 및 근거
- ORD 기록
- ord-7a115c64888a4ebcb4f269e186d5cbbd
- 출처 데이터셋
- uspto-grants-2010_06
- 특허 번호
- US07745623B2
연결된 노트
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