Reaktionsgleichung
C([O:3][C:4](=[O:19])[CH:5]([O:16][CH2:17][CH3:18])[CH2:6][C:7]1[CH:15]=[C:14]2[C:10]([CH:11]=[CH:12][NH:13]2)=[CH:9][CH:8]=1)C.Cl[CH2:21][C:22]1[N:23]=[C:24]([C:27]2[CH:32]=[CH:31][C:30]([CH:33]([CH3:35])[CH3:34])=[CH:29][CH:28]=2)[S:25][CH:26]=1>>[CH2:17]([O:16][CH:5]([CH2:6][C:7]1[CH:15]=[C:14]2[C:10]([CH:11]=[CH:12][N:13]2[CH2:21][C:22]2[N:23]=[C:24]([C:27]3[CH:32]=[CH:31][C:30]([CH:33]([CH3:35])[CH3:34])=[CH:29][CH:28]=3)[S:25][CH:26]=2)=[CH:9][CH:8]=1)[C:4]([OH:3])=[O:19])[CH3:18]Komponenten
3
Versuchsvorschrift
In analogy to the procedure described in example 44, rac-2-ethoxy-3-(1H-indol-6-yl)-propionic acid ethyl ester (preparation 11) was reacted with 4-chloromethyl-2-(4-isopropyl-phenyl)-thiazole to give rac-2-ethoxy-3-{1-[2-(4-isopropyl-phenyl)-thiazol-4-ylmethyl]-1H-indol-6-yl}-propionic acid as yellow viscous oil.
Quellen und Nachweise
- ORD-Eintrag
- ord-6b99233aa2be4d6781dd193b809309ec
- Quelldatensatz
- uspto-grants-2005_05
- Patentnummer
- US06890947B2
Verknüpfte Notizen
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