D-Phenylalanine → Dl-Phenylalanine
Reaction equation
[C:1]([C@H:4]([NH:12]C1C(C(O)=O)=CC2C(=CC=C(Cl)C=2)N=1)[CH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)([OH:3])=[O:2].N[C@@H](C(O)=O)CC1C=CC=CC=1>>[NH2:12][CH:4]([C:1]([OH:3])=[O:2])[CH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1Participants
3
Procedure
Analysis of the sample enriched by (2%) substance obtained according to the procedure described in Example 6 (2-((R)-1-Carboxy-2-phenyl-ethylamino)-6-chloro-quinoline-3-carboxylic acid, obtained using D-phenylalanine as a starting material) resulted in an increase of peak with Rt 39.32 min.
Workup
- customAnalysis of the sample enriched by (2%) substance obtained
- customobtained
- customresulted in
- temperaturean increase of peak with Rt 39.32 min.
Sources & evidence
- ORD record
- ord-78902ca8184c412faa777da9987b6ee0
- Source dataset
- uspto-grants-2012_10
- Patent number
- US08288549B2
Reaction notes
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