Sodium Iodide → Ethyl 2-iodomethyl-6,7-dimethoxy-4-(3,4-dimethoxyphenyl)quinoline-3-carboxylate
반응식
[I-:1].[Na+].Cl[C:4]1[C:13]([C:14]([O:16][CH2:17][CH3:18])=[O:15])=[C:12]([C:19]2[CH:24]=[CH:23][C:22]([O:25][CH3:26])=[C:21]([O:27][CH3:28])[CH:20]=2)[C:11]2[C:6](=[CH:7][C:8]([O:31][CH3:32])=[C:9]([O:29][CH3:30])[CH:10]=2)[N:5]=1.[CH2:33](C(C)=O)C>>[CH3:30][O:29][C:9]1[CH:10]=[C:11]2[C:6](=[CH:7][C:8]=1[O:31][CH3:32])[N:5]=[C:4]([CH2:33][I:1])[C:13]([C:14]([O:16][CH2:17][CH3:18])=[O:15])=[C:12]2[C:19]1[CH:24]=[CH:23][C:22]([O:25][CH3:26])=[C:21]([O:27][CH3:28])[CH:20]=1참가 물질
반응 조건
- 온도
- 80 °C
실험 절차
A mixture of sodium iodide (1.68 g) and methyl ethyl ketone (15 ml) was stirred at 80° C. for 1 hour. Then ethyl 2-chloro-6,7-dimethoxy-4-(3,4-dimethoxyphenyl)quinoline-3-carboxylate (2.0 g) was added, and the resulting mixture was stirred at the same temperature for 12 hours. The insoluble materials were filtered off, and the filtrate was concentrated under reduced pressure. The residue was poured into water and extracted with ethyl acetate. The ethyl acetate layer was washed with water and dried (MgSO4), and the solvent was distilled off. The residual oil was subjected to column chromatography on silica gel. From the fraction eluted with chloroform/ethyl acetate (1:1, v/v), ethyl 6,7-dimethoxy-4-(3,4-dimethoxyphenyl)-2-iodomethylquinoline-3-carboxylate (1.4 9, 58%) was obtained and recrystallized from ethyl acetate/hexane.
후처리
- stirringthe resulting mixture was stirred at the same temperature for 12 hours
- filtrationThe insoluble materials were filtered off
- concentrationthe filtrate was concentrated under reduced pressure
- additionThe residue was poured into water
- extractionextracted with ethyl acetate
- washThe ethyl acetate layer was washed with water
- dry with materialdried (MgSO4)
- distillationthe solvent was distilled off
- washFrom the fraction eluted with chloroform/ethyl acetate (1:1
출처 및 근거
- ORD 기록
- ord-a29e968431e34d57b21fce96c04fa55c
- 출처 데이터셋
- uspto-grants-1999_09
- 특허 번호
- US05948782
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