Reaktionsgleichung
C1([C@@H](N2CCCC2)CO)C=CC=CC=1.[C:15]1([C@H:21](O)[CH2:22][N:23]2[CH2:27][CH2:26][CH2:25][CH2:24]2)[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1.[CH3:29][NH:30][C:31]1[CH:40]=[CH:39][C:34]([C:35]([O:37][CH3:38])=[O:36])=[CH:33][CH:32]=1>>[C:15]1([C@H:21]([N:30]([C:31]2[CH:40]=[CH:39][C:34]([C:35]([O:37][CH3:38])=[O:36])=[CH:33][CH:32]=2)[CH3:29])[CH2:22][N:23]2[CH2:27][CH2:26][CH2:25][CH2:24]2)[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1Komponenten
4
Versuchsvorschrift
This was prepared from the mixture of 2-(R)-phenyl-2-(pyrrolidin-1-yl)ethanol and 1-(S)-phenyl-2-(pyrrolidin-1-yl)ethanol and methyl 4-methylaminobenzoate in 52% yield according to a procedure similar to that described in Example 1 (i).
Quellen und Nachweise
- ORD-Eintrag
- ord-e3be257a7e59409cbe81a130f59512b1
- Quelldatensatz
- uspto-grants-2001_10
- Patentnummer
- US06307061B2
Verknüpfte Notizen
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