Reaktionsgleichung
[Cl:1][C:2]1[CH:3]=[C:4]([CH:6]=[CH:7][C:8]=1[Cl:9])[NH2:5].[C:10]([O:15][CH2:16][CH:17]([CH3:19])[CH3:18])(=[O:14])[C:11]([CH3:13])=O>>[CH2:16]([O:15][C:10](=[O:14])[C@H:11]([CH3:13])[NH:5][C:4]1[CH:6]=[CH:7][C:8]([Cl:9])=[C:2]([Cl:1])[CH:3]=1)[CH:17]([CH3:19])[CH3:18]Komponenten
3
Versuchsvorschrift
Following General Procedure AA above and using 3,4-dichloroaniline (Aldrich) and iso-butyl pyruvate (prepared by following General Procedure AO above), the title compound was prepared as an oil. The reaction was monitored by tlc on silica gel (Rf=0.55 in 25% EtOAc/hexanes) and purification was by preparative plate chromatography (silica gel using 25% EtOAc/hexanes as the eluant).
Aufarbeitung
- customThe reaction was monitored by tlc on silica gel (Rf=0.55 in 25% EtOAc/hexanes) and purification
Quellen und Nachweise
- ORD-Eintrag
- ord-6888b8e4ce4c4a608f80013bbcb300d7
- Quelldatensatz
- uspto-grants-2005_02
- Patentnummer
- US06849650B2
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