반응식
[CH2:1]([O:3][C:4]1[CH:11]=[CH:10][CH:9]=[C:8]([CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26])[C:5]=1[CH:6]=O)[CH3:2].[C:27]([O:33][CH:34]([CH3:36])[CH3:35])(=[O:32])[CH2:28][C:29]([CH3:31])=O.C(O)(=O)C.N1CCCCC1.[CH3:47][CH2:48][O:49][C:50](/[CH:52]=[C:53](\[NH2:55])/[CH3:54])=[O:51]>C(O)CCC>[CH2:1]([O:3][C:4]1[CH:11]=[CH:10][CH:9]=[C:8]([CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26])[C:5]=1[CH:6]1[C:28]([C:27]([O:33][CH:34]([CH3:36])[CH3:35])=[O:32])=[C:29]([CH3:31])[NH:55][C:53]([CH3:54])=[C:52]1[C:50]([O:49][CH2:48][CH3:47])=[O:51])[CH3:2]참가 물질
반응물 5
생성물 1
시약·촉매·용매 1
실험 절차
2-Ethoxy-6-pentadecyl benzaldehyde (3 g, 8.3 mmol) and isopropyl acetoacetate (1.19 g, 8.3 mmol) were dissolved in n-butanol (20 mL). Acetic acid (0.5 g, 8.3 mmol) and piperidine (0.7 g, 8.3 mmol) were added and stirred at room temperature for 3-4 hrs. Ethyl-3-amino crotonate (1.08 g, 8.3 mmol) was then added and refluxed for 10 hrs. n-Butanol was evaporated and reaction mixture was washed with distilled water and extracted with dichloromethane (10 mL). Organic layer was dried over sodium sulfate, evaporated and compound was purified by column chromatography using silica gel (100-200 mesh) with hexane:EtOAc (94:6) solvent system to give ethyl isopropyl 1,4-dihydro-4-(2′-ethoxy-6′-pentadecylphenyl)-2,6-dimethyl-3,5-pyridine dicarboxylate as viscous liquid.
후처리
- temperaturerefluxed for 10 hrs
- customn-Butanol was evaporated
- customreaction mixture
- washwas washed with distilled water
- extractionextracted with dichloromethane (10 mL)
- dry with materialOrganic layer was dried over sodium sulfate
- customevaporated
- customcompound was purified by column chromatography
출처 및 근거
- ORD 기록
- ord-38a1014fd89d4d9780acdb158fc26e7b
- 출처 데이터셋
- uspto-grants-2012_01
- 특허 번호
- US08106062B1
연결된 노트
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