3-Bromo-5-ethoxy-4-hydroxybenzaldehyde → 4-(3-bromo-5-ethoxy-4-hydroxy-phenyl)-2-methyl-5-oxo-7-propyl-1,4,5,6,7,8-hexahydro-quinoline-3-carboxylic acid (1S)-[1-(4-methoxy-phenyl)-ethyl]-amide

HRID 910763Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 910763
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C@@H:9]([NH:11][C:12](=[O:17])[CH:13]=[C:14]([NH2:16])[CH3:15])[CH3:10])=[CH:5][CH:4]=1.[Br:18][C:19]1[CH:20]=[C:21]([CH:24]=[C:25]([O:28][CH2:29][CH3:30])[C:26]=1[OH:27])[CH:22]=O.[CH2:31]([CH:34]1[CH2:39][C:38](=[O:40])[CH2:37][C:36](=O)[CH2:35]1)[CH2:32][CH3:33]>C(O)C>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([C@@H:9]([NH:11][C:12]([C:13]2[CH:22]([C:21]3[CH:24]=[C:25]([O:28][CH2:29][CH3:30])[C:26]([OH:27])=[C:19]([Br:18])[CH:20]=3)[C:37]3[C:38](=[O:40])[CH2:39][CH:34]([CH2:31][CH2:32][CH3:33])[CH2:35][C:36]=3[NH:16][C:14]=2[CH3:15])=[O:17])[CH3:10])=[CH:7][CH:8]=1

Komponenten

5

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

A mixture of (S)-3-amino-but-2-enoic acid [1-(4-methoxy-phenyl)-ethyl]-amide (10 g), 3-bromo-5-ethoxy-4-hydroxy-benzaldehyde (10.4 g) and 5-propylcyclohexane-1,3-dione (6.5 g) in ethanol (150 ml) was stirred at 80° C. for 18 hr. The mixture was concentrated in vacuo. The residue was dissolved in toluene (100 ml) and dichloromethane (50 ml) and evaporated until a precipitated formed. The solid obtained was then crystallized in EtOAc.

Aufarbeitung

  1. concentrationThe mixture was concentrated in vacuo
  2. dissolutionThe residue was dissolved in toluene (100 ml)
  3. customdichloromethane (50 ml) and evaporated until a precipitated
  4. customformed
  5. customThe solid obtained
  6. customwas then crystallized in EtOAc

Quellen und Nachweise

ORD-Eintrag
ord-a429293d35a64bc08d2dab2e8e49d804
Quelldatensatz
uspto-grants-2011_09
Patentnummer
US08022218B2

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