3-Methylpentanoic acid → N-(3-methylpentanoyl)-L-alanine Isobutyl Ester
Reaction equation
[CH3:1][CH:2]([CH2:7][CH3:8])[CH2:3][C:4]([OH:6])=O.Cl.[CH2:10]([O:14][C:15](=[O:19])[C@H:16]([CH3:18])[NH2:17])[CH:11]([CH3:13])[CH3:12]>>[CH2:10]([O:14][C:15](=[O:19])[C@H:16]([CH3:18])[NH:17][C:4](=[O:6])[CH2:3][CH:2]([CH3:1])[CH2:7][CH3:8])[CH:11]([CH3:13])[CH3:12]Participants
3
Procedure
Following General Procedure B and using 3-methylpentanoic acid (Aldrich) and L-alanine iso-butyl ester hydrochloride (from Example B above), the title compound was prepared as an oil. The reaction was monitored by tlc on silica gel and purification was by extraction with Et2O followed by washes with aqueous K2CO3 and aqueous HCl.
Workup
- customThe reaction was monitored by tlc on silica gel and purification
- extractionwas by extraction with Et2O
Sources & evidence
- ORD record
- ord-df3c581e8dfd48e482f5e02438e87d1b
- Source dataset
- uspto-grants-2001_11
- Patent number
- US06313152B1
Reaction notes
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