L-Malic Acid → HCID 9891068, compound
Reaction equation
[CH3:1][N:2]([CH3:35])[CH2:3][CH2:4][N:5]([CH2:33]C)[C:6](=[O:32])[CH2:7][O:8][C@H:9]1[C:12]([CH2:15][CH3:16])([CH2:13][CH3:14])[C:11](=[O:17])[N:10]1[C:18]([NH:20][C@@H:21]([C:25]1[CH:30]=[CH:29][C:28]([CH3:31])=[CH:27][CH:26]=1)[CH2:22][CH2:23][CH3:24])=[O:19].C(O)(=O)[C@H](CC(O)=O)O>>[CH3:35][N:2]([CH3:1])[CH2:3][CH2:4][N:5]([CH3:33])[C:6](=[O:32])[CH2:7][O:8][C@H:9]1[C:12]([CH2:13][CH3:14])([CH2:15][CH3:16])[C:11](=[O:17])[N:10]1[C:18]([NH:20][C@@H:21]([C:25]1[CH:26]=[CH:27][C:28]([CH3:31])=[CH:29][CH:30]=1)[CH2:22][CH2:23][CH3:24])=[O:19]Participants
3
Procedure
2-(S)-[2-[[2-(Dimethylamino)ethyl]ethylamino]-2-oxoethoxy]-3,3-diethyl-N-[1-(R)-(4-methylphenyl) butyl]-4-oxo-1-azetidinecarboxamide or the L-malic acid salt thereof; or
Sources & evidence
- ORD record
- ord-6419c54b94fe4e48b633189a040221ea
- Source dataset
- uspto-grants-1994_09
- Patent number
- US05348953
Reaction notes
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