Alanine methyl ester hydrochloride → N-[N-(3,5-dichlorophenyl)-D,L-alanyl]-L-alanine methyl ester
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([NH:9][CH:10]([C:12]([OH:14])=O)[CH3:11])[CH:5]=[C:6]([Cl:8])[CH:7]=1.Cl.[CH3:16][O:17][C:18](=[O:22])[C@H:19]([CH3:21])[NH2:20]>>[CH3:16][O:17][C:18](=[O:22])[C@H:19]([CH3:21])[NH:20][C:12](=[O:14])[CH:10]([CH3:11])[NH:9][C:4]1[CH:5]=[C:6]([Cl:8])[CH:7]=[C:2]([Cl:1])[CH:3]=1Participants
3
Procedure
Following General Procedure D and using N-(3,5 -dichlorophenyl)-D,L-alanine (from Example B above) and L-alanine methyl ester hydrochloride (Sigma), the title compound was prepared as a oil. The reaction product was purified by silica gel chromatography using 50% ethyl acetate/hexane.
Workup
- customThe reaction product was purified by silica gel chromatography
Sources & evidence
- ORD record
- ord-a5b5c5af328d47cdbcc205ad0105b16a
- Source dataset
- uspto-grants-2000_08
- Patent number
- US06096782
Reaction notes
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