L-Alanine ethyl ester → N-[(3,5difluorophenyl)acetyl]alanine Ethyl Ester

HRID 1884975Notes

Reaction equation

HRID 1884975 reaction equation
[F:1][C:2]1[CH:3]=[C:4]([CH2:9][C:10]([OH:12])=O)[CH:5]=[C:6]([F:8])[CH:7]=1.[CH2:13]([O:15][C:16](=[O:20])[C@H:17]([CH3:19])[NH2:18])[CH3:14]>>[CH2:13]([O:15][C:16](=[O:20])[C@H:17]([CH3:19])[NH:18][C:10](=[O:12])[CH2:9][C:4]1[CH:5]=[C:6]([F:8])[CH:7]=[C:2]([F:1])[CH:3]=1)[CH3:14]

Participants

3

Procedure

Following General Procedure G and using 3,5difluorophenylacetic acid (Aldrich) and alanine ethyl ester (Aldrich), the title compound was prepared as a solid with a melting point of 93°-95° C. The reaction was monitored by dc on silica gel (Rf=0.8 in EtOAC) and purification was by chromatography on silica gel using EtOAc as the eluant followed by recrystallization from-1-chlorobutane.

Workup

  1. customThe reaction was monitored by dc on silica gel (Rf=0.8 in EtOAC) and purification
  2. customfollowed by recrystallization from-1-chlorobutane

Sources & evidence

ORD record
ord-bd51ab56f95a46ba86a5921cf922348d
Source dataset
uspto-grants-2004_07
Patent number
US06767918B2

Reaction notes

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