HCID 68821379, compound → HCID 68820910, compound
Reaction equation
[Cl:1][C:2]1[CH:27]=[CH:26][CH:25]=[C:24](F)[C:3]=1[C:4]([NH:6][C@H:7]([C:21]([OH:23])=[O:22])[CH2:8][NH:9][C:10](=[O:20])[CH2:11][CH:12]([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)[CH3:13])=[O:5].[Cl:29]C1C=CC=C(Cl)C=1C(N[C@H](C(O)=O)CNC([C@@H]1CCC(=O)O1)=O)=O>>[Cl:1][C:2]1[CH:27]=[CH:26][CH:25]=[C:24]([Cl:29])[C:3]=1[C:4]([NH:6][C@H:7]([C:21]([OH:23])=[O:22])[CH2:8][NH:9][C:10](=[O:20])[CH2:11][CH:12]([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)[CH3:13])=[O:5]Participants
3
Procedure
N-(2-chloro-6-fluorobenzoyl)-3-[(3RS)-3-phenylbutanoyl]amino-L-alanine) or k is 0 (for example N-(2,6-dichlorobenzoyl)-3-[(2S)-5-oxotetrahydrofuran-2-carbonyl]amino-L-alanine;
Sources & evidence
- ORD record
- ord-fa7fd8575fb345d2b202808a980dc195
- Source dataset
- uspto-grants-2004_10
- Patent number
- US06803384B2
Reaction notes
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