Reaktionsgleichung
[OH:1][C:2]1[CH2:7][CH:6]([C:8]2[C:13]([CH3:14])=[CH:12][CH:11]=[CH:10][C:9]=2[CH3:15])[CH2:5][C:4](=[O:16])[C:3]=1[C:17](=O)[CH2:18][CH3:19].Cl[S:22]([OH:25])(=O)=[O:23].[CH3:26][NH:27][CH3:28].Cl.[CH2:30]([O:32][NH2:33])[CH3:31]>>[CH2:30]([O:32][N:33]=[C:17]([C:3]1[C:4](=[O:16])[CH2:5][CH:6]([C:8]2[C:13]([CH3:14])=[CH:12][CH:11]=[C:10]([S:22](=[O:25])(=[O:23])[N:27]([CH3:28])[CH3:26])[C:9]=2[CH3:15])[CH2:7][C:2]=1[OH:1])[CH2:18][CH3:19])[CH3:31]Komponenten
5
Versuchsvorschrift
2-[1-(Ethoxyimino)propyl]-3-hydroxy-5-(2,6-dimethyl-3-dimethylsulfamoylphenyl)cyclohex-2-en-1-one (5) was prepared from 3-hydroxy-5-(2,6-dimethylphenyl)-2-propionylcyclohex-2-en-1-one, chlorosulfonic acid, dimethylamine, and ethoxyamine hydrochloride following essentially the same procedure as that described in Example 5.
Quellen und Nachweise
- ORD-Eintrag
- ord-5cb6474f52844c2bba022377de34628a
- Quelldatensatz
- uspto-grants-1988_08
- Patentnummer
- US04767879
Verknüpfte Notizen
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