Alanine methyl ester hydrochloride → HCID 54367074, compound
Reaction equation
Cl.[CH3:2][O:3][C:4](=[O:8])[C@H:5]([CH3:7])[NH2:6].[F:9][C:10]1[CH:11]=[C:12]([NH:17][CH:18]([C:20](O)=[O:21])[CH3:19])[CH:13]=[C:14]([F:16])[CH:15]=1>>[CH3:2][O:3][C:4](=[O:8])[C@H:5]([CH3:7])[NH:6][C:20](=[O:21])[CH:18]([CH3:19])[NH:17][C:12]1[CH:13]=[C:14]([F:16])[CH:15]=[C:10]([F:9])[CH:11]=1Participants
3
Procedure
Following General Procedure E and using L-alanine methyl ester hydrochloride (Sigma) and N-(3,5-difluorophenyl)-D,L-alanine (from Example C above), the title compound was prepared as a solid (mp=93-95° C.). The reaction was monitored by tlc (Rf=0.4 in 3% methanol/methylene chloride) and purification of this compound was by flash chromatography with 3% methanol/methylene chloride.
Workup
- customThe reaction was monitored by tlc (Rf=0.4 in 3% methanol/methylene chloride) and purification of this compound
Sources & evidence
- ORD record
- ord-6133bf135f4b443892a6efe0d0ac0d9f
- Source dataset
- uspto-grants-2000_08
- Patent number
- US06096782
Reaction notes
Loading…