3,5-bis(2-oxopyrrolidin-1-yl)benzoic Acid → HCID 69589702, compound
Reaction equation
O=C1CCCN1C1C=C(C=C(N2CCCC2=O)C=1)C(O)=O.[C@@H:22]([O:26][C:27]1[CH:28]=[C:29]([CH:34]=[C:35]([N:37]2[CH2:41][CH2:40][CH2:39][C:38]2=[O:42])[CH:36]=1)[C:30]([O:32]C)=[O:31])([CH2:24][CH3:25])[CH3:23]>>[C@@H:22]([O:26][C:27]1[CH:28]=[C:29]([CH:34]=[C:35]([N:37]2[CH2:41][CH2:40][CH2:39][C:38]2=[O:42])[CH:36]=1)[C:30]([OH:32])=[O:31])([CH2:24][CH3:25])[CH3:23]Participants
3
Procedure
Prepared in an analogous manner to D8 from methyl 3-((S)-sec-butyloxy)-5-(2-oxopyrrolidin-1-yl)benzoate (D44).
Sources & evidence
- ORD record
- ord-8b53ab3428f54dfa897dd23ea60ab8f3
- Source dataset
- uspto-grants-2006_01
- Patent number
- US06992103B2
Reaction notes
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