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 BB and using 3-methylpentanoic acid (Aldrich) and L-alanine iso-butyl ester hydrochloride (from Example BB 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-eb4f4581a8134023993611fb790a5a10
- Source dataset
- uspto-grants-2003_12
- Patent number
- US06667305B1
Reaction notes
Loading…