Reaktionsgleichung
[CH2:1]([O:3][C:4](=[O:25])[C:5]1[CH:10]=[CH:9][C:8]([NH:11][C:12]2[CH:21]=[CH:20][C:19]3[C:18]([CH3:22])=[CH:17][CH2:16][C:15]([CH3:24])([CH3:23])[C:14]=3[CH:13]=2)=[CH:7][CH:6]=1)[CH3:2].[CH:26](=O)[CH3:27]>>[CH2:1]([O:3][C:4](=[O:25])[C:5]1[CH:6]=[CH:7][C:8]([N:11]([CH2:26][CH3:27])[C:12]2[CH:21]=[CH:20][C:19]3[C:18]([CH3:22])=[CH:17][CH2:16][C:15]([CH3:24])([CH3:23])[C:14]=3[CH:13]=2)=[CH:9][CH:10]=1)[CH3:2]Komponenten
3
Versuchsvorschrift
Following General Procedure M, 4-(5,8,8-trimethyl-7,8-dihydro-naphthalen-2-ylamino)-benzoic acid ethyl ester (Compound 65, 38 mg, 0.11 mmol), was reacted to with acetaldehyde to give the title compound as a yellow oil.
Quellen und Nachweise
- ORD-Eintrag
- ord-249ac15311214d5a86ffe284ecb32139
- Quelldatensatz
- uspto-grants-2003_09
- Patentnummer
- US06613917B1
Verknüpfte Notizen
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