반응식
[CH:1]([NH:4][C:5]([N:7]1[CH2:12][CH2:11][CH:10]([CH2:13][C:14]2[CH:19]=[CH:18][C:17]([NH2:20])=[CH:16][CH:15]=2)[CH2:9][CH2:8]1)=[O:6])([CH3:3])[CH3:2].S(O)(O)(=O)=O.Cl[C:27]1[NH:28][CH2:29][CH2:30][N:31]=1>CC(O)C>[CH:1]([NH:4][C:5]([N:7]1[CH2:8][CH2:9][CH:10]([CH2:13][C:14]2[CH:15]=[CH:16][C:17]([NH:20][C:27]3[NH:31][CH2:30][CH2:29][N:28]=3)=[CH:18][CH:19]=2)[CH2:11][CH2:12]1)=[O:6])([CH3:3])[CH3:2]참가 물질
실험 절차
A mixture of 4-(1-isopropylaminocarbonylpiperidin-4-ylmethyl)-phenylamine (0.64 g, 2.31 mmol) and 2-chloro-2-imidazoline sulfate (0.70 g, 3.47 mmol) in 2-propanol (20 mL) was heated under reflux for 30 minutes. The reaction mixture was concentrated in vacuo. The residue was diluted with water, basified with 10% sodium hydroxide solution and extracted into dichloromethane. The organic layer was washed with water and brine, dried (Na2SO4), and concentrated in vacuo. The crude product was chromatographed on neutral aluminum oxide, eluting with 5% methanol/dichloromethane, and crystallized from ethyl acetate containing some ethanol, to give 2-[4-(1-isopropylaminocarbonylpiperidin-4-ylmethyl)-phenyl]amino-imidazoline (0.47 g, 59%) as a white solid, m.p. 191–192° C.
후처리
- temperaturewas heated
- temperatureunder reflux for 30 minutes
- concentrationThe reaction mixture was concentrated in vacuo
- additionThe residue was diluted with water
- extractionextracted into dichloromethane
- washThe organic layer was washed with water and brine
- dry with materialdried (Na2SO4)
- concentrationconcentrated in vacuo
- customThe crude product was chromatographed on neutral aluminum oxide
- washeluting with 5% methanol/dichloromethane
- customcrystallized from ethyl acetate containing some ethanol
출처 및 근거
- ORD 기록
- ord-f4967b3a56184524b02094eb42413ce2
- 출처 데이터셋
- uspto-grants-2006_11
- 특허 번호
- US07141584B2
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