Reaktionsgleichung
[Cl:1][C:2]1[CH:9]=[C:8](F)[CH:7]=[CH:6][C:3]=1[C:4]#[N:5].Cl.[CH2:12]([O:16][C:17](=[O:21])[CH:18]([CH3:20])[NH2:19])[CH:13]([CH3:15])[CH3:14]>>[CH2:12]([O:16][C:17](=[O:21])[C@H:18]([CH3:20])[NH:19][C:8]1[CH:7]=[CH:6][C:3]([C:4]#[N:5])=[C:2]([Cl:1])[CH:9]=1)[CH:13]([CH3:15])[CH3:14]Komponenten
3
Versuchsvorschrift
Following General Procedure AP above and using 2-chloro-4-fluorobenzonitrile (Aldrich) and D,L-alanine iso-butyl ester hydrochloride (from Example AA above), the title compound was prepared. The product was recovered by column chromatography on silica gel using 1:5 EtOAc/hexanes as the eluant.
Aufarbeitung
- customThe product was recovered by column chromatography on silica gel using 1:5 EtOAc/hexanes as the eluant
Quellen und Nachweise
- ORD-Eintrag
- ord-a4bbed5dd2044f3fadb7ea98748fef7c
- Quelldatensatz
- uspto-grants-2005_02
- Patentnummer
- US06849650B2
Verknüpfte Notizen
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