Reaktionsgleichung
[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][N:11]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=2[CH2:20][CH2:21][CH:22]([CH3:24])[CH3:23])[C:10](=[O:25])[CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].C([N:33](CC1C=CC=CC=1)[CH:34]([CH2:37][C:38]1[CH:43]=[C:42]([F:44])[CH:41]=[C:40]([F:45])[CH:39]=1)[CH:35]=[O:36])C1C=CC=CC=1>>[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][N:11]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=2[CH2:20][CH2:21][CH:22]([CH3:23])[CH3:24])[C:10](=[O:25])[C@@H:9]1[C@@H:35]([OH:36])[C@@H:34]([NH2:33])[CH2:37][C:38]1[CH:39]=[C:40]([F:45])[CH:41]=[C:42]([F:44])[CH:43]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2]Komponenten
3
Versuchsvorschrift
The title is prepared by reacting 4-[2-(3-methyl-butyl)-phenyl]-3-oxo-piperazine-1-carboxylic acid tert-butyl ester with 2-(dibenzylamino)-3-(3,5-difluorophenyl)-propanal essentially as described in Preparation 41.
Aufarbeitung
- customThe title is prepared
- customas described in Preparation 41
Quellen und Nachweise
- ORD-Eintrag
- ord-1a3a372096624bfaa657a10174cfa929
- Quelldatensatz
- uspto-grants-2009_11
- Patentnummer
- US07618978B2
Verknüpfte Notizen
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