Reaktionsgleichung
COC.O[C:5]1[CH:10]=[CH:9][C:8]([C:11]2[N:12]=[C:13]([CH2:22][CH2:23][C:24]([OH:26])=[O:25])[O:14][C:15]=2[C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)=[CH:7][CH:6]=1>C(Cl)(Cl)Cl.CC(CC(C)C)=O.C(O)(=O)C>[CH:5]1[CH:10]=[CH:9][C:8]([C:11]2[N:12]=[C:13]([CH2:22][CH2:23][C:24]([OH:26])=[O:25])[O:14][C:15]=2[C:16]2[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=2)=[CH:7][CH:6]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Rf 0.50 silica gel 60 F254 chloroform:methylisobutylketone:acetic acid 50:50:1 A mixed melting point run with an authentic sample of the methyl ether of 4-(4-hydroxyphenyl)-5-phenyl-2-oxazolepropanoic acid (obtained from the metabolite of oxaprozin as disclosed by Janssen et al., Drug Metabolism and Disposition, 6, 495 (1978)), gave m.p. 92°-108° C., clearly demonstrating the lack of identity with the known metabolite. This, coupled with the identity of the 4'-methoxybenzoin starting material characterized the methyl ether as 5-(4-methoxy)-4-phenyl-2-oxazolepropanoic acid.
Quellen und Nachweise
- ORD-Eintrag
- ord-8c506356e9af4faa9b08c412bac81255
- Quelldatensatz
- uspto-grants-1987_04
- Patentnummer
- US04659728
Verknüpfte Notizen
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