Hydrochloric Acid → Methyl 1,4,5,7-tetrahydro-4-(4-chlorophenyl)-2-methyl-5-oxo-furo[3,4-b]-pyridine-3-carboxylate
반응식
[Cl:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=O)=[CH:4][CH:3]=1.C(O[CH2:14][C:15](=O)[CH2:16][C:17]([O:19][CH2:20]C)=[O:18])(=O)C.[NH2:23]/[C:24](/[CH3:30])=[CH:25]\[C:26]([O:28]C)=[O:27].Cl>C(O)(C)C>[Cl:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]2[C:16]([C:17]([O:19][CH3:20])=[O:18])=[C:15]([CH3:14])[NH:23][C:24]3[CH2:30][O:28][C:26](=[O:27])[C:25]2=3)=[CH:4][CH:3]=1참가 물질
6
실험 절차
3 g (21.3 mmol) of 4-chlorobenzaldehyde, 4.0 g (21.3 mmol) of ethyl 4-acetoxyacetoacetate and 2.5 g (21.3 mmol) of methyl 3-aminocrotonate are dissolved in 40 ml of isopropanol and heated to reflux for 12 h. The mixture is then treated with 10 ml of dilute aqueous HCl and heated to reflux for a further 30 min. The mixture is partitioned between toluene and water. Drying (MgSO4) and concentration of the organic phase yields a white solid which is purified by filtration through 50 g of silica gel (ethyl acetate/petroleum ether 1+1) and subsequent recrystallization from ethyl acetate/petroleum ether. 2.6 g (8.13 mmol, 38%) are obtained.
후처리
- temperatureheated
- temperatureto reflux for 12 h
- temperatureheated
- temperatureto reflux for a further 30 min
- customThe mixture is partitioned between toluene and water
- dry with materialDrying (MgSO4) and concentration of the organic phase
- customyields a white solid which
- filtrationis purified by filtration through 50 g of silica gel (ethyl acetate/petroleum ether 1+1) and subsequent recrystallization from ethyl acetate/petroleum ether
- custom2.6 g (8.13 mmol, 38%) are obtained
출처 및 근거
- ORD 기록
- ord-dd512865b5444fb2a48bef59e4b99114
- 출처 데이터셋
- uspto-grants-2001_02
- 특허 번호
- US06194428B1
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