Reaktionsgleichung
CO[C:3](=[O:8])[CH2:4][C:5](=O)[CH3:6].Br[CH2:10][C:11]([C:13]1[CH:18]=[C:17]([C:19]([F:22])([F:21])[F:20])[CH:16]=[CH:15][C:14]=1[F:23])=O.[CH3:24][C:25]1([CH3:32])[O:29][CH:28]([CH2:30][NH2:31])[CH2:27][O:26]1.[CH:33]1([NH2:39])[CH2:38][CH2:37][CH2:36][CH2:35][CH2:34]1>>[CH:33]1([NH:39][C:3]([C:4]2[CH:10]=[C:11]([C:13]3[CH:18]=[C:17]([C:19]([F:22])([F:21])[F:20])[CH:16]=[CH:15][C:14]=3[F:23])[N:31]([CH2:30][CH:28]3[CH2:27][O:26][C:25]([CH3:32])([CH3:24])[O:29]3)[C:5]=2[CH3:6])=[O:8])[CH2:38][CH2:37][CH2:36][CH2:35][CH2:34]1Komponenten
5
Edukt 4
Produkt 1
Versuchsvorschrift
The title compound was synthesized in analogy to example 7, using 3-oxo-butyric acid methyl ester as compound of formula R, 2-bromo-1-[2-fluoro-5-(trifluoromethyl)-phenyl]-ethanone as compound of formula S, 2,2-dimethyl-1,3-dioxolan-4-methylamine as R3—(CH2)m—NH2 and 1-cyclohexylamine as R1R2NH, MS (ISP) 483.6 (M+H)+.
Quellen und Nachweise
- ORD-Eintrag
- ord-e04cebfbd53b4e869c47bdd57b91f870
- Quelldatensatz
- uspto-grants-2009_07
- Patentnummer
- US07563910B2
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