Reaction equation
[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]Participants
3
Procedure
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).
Workup
- customThe reaction was monitored by tlc on silica gel (Rf=0.55 in 25% EtOAc/hexanes) and purification
Sources & evidence
- ORD record
- ord-9f1db41788c449c3a90acf91524b0cb7
- Source dataset
- uspto-grants-2008_06
- Patent number
- US07390801B2
Linked notes
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