Diisopropylethylamine → 4-(2-(Pyridin-2-yl)ethyl)piperazin-2-one
반응식
[NH:1]1[CH2:6][CH2:5][NH:4][CH2:3][C:2]1=[O:7].Cl.Cl[CH2:10][CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][N:13]=1.CCN(C(C)C)C(C)C>>[N:13]1[CH:14]=[CH:15][CH:16]=[CH:17][C:12]=1[CH2:11][CH2:10][N:4]1[CH2:5][CH2:6][NH:1][C:2](=[O:7])[CH2:3]1참가 물질
4
실험 절차
Piperazinone (2.2 g, 22 mmol), 2-(2-chloroethyl)pyridine hydrochloride (3.9 g, 22 mmol) and i-Pr2NEt (5.67 g, 7.6 mL, 44 mmol) were heated at reflux for 16 h. The mixture was concentrated, and the residue was purified by column chromatography (80 g ISCO column eluting with methylene chloride and a 10:1 methanol/ammonium hydroxide mixture; gradient 100% methylene chloride to 90% methylene chloride) to provide the title compound (1.5 g, 33%) as a yellow solid: ESI MS m/z 206 [M+H]+.
후처리
- temperatureat reflux for 16 h
- concentrationThe mixture was concentrated
- customthe residue was purified by column chromatography (80 g ISCO column
- washeluting with methylene chloride
출처 및 근거
- ORD 기록
- ord-552a05fd08d54d179a77a2bab1017dea
- 출처 데이터셋
- uspto-grants-2014_04
- 특허 번호
- US08697700B2
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