Hydrochloric Acid → Methyl 1,4,5,7-tetrahydro-4-(4-chlorophenyl)-2-methyl-5-oxo-furo[3,4-b]-pyridine-3-carboxylate

HRID 636534노트

반응식

HRID 636534 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]=1

참가 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

  1. temperatureheated
  2. temperatureto reflux for 12 h
  3. temperatureheated
  4. temperatureto reflux for a further 30 min
  5. customThe mixture is partitioned between toluene and water
  6. dry with materialDrying (MgSO4) and concentration of the organic phase
  7. customyields a white solid which
  8. filtrationis purified by filtration through 50 g of silica gel (ethyl acetate/petroleum ether 1+1) and subsequent recrystallization from ethyl acetate/petroleum ether
  9. 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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