3,5-bis(2-oxopyrrolidin-1-yl)benzoic Acid → 3-Cyclobutyloxy-5-(2-oxopyrrolidin-1-yl)benzoic acid
Reaction equation
O=C1CCCN1C1C=C(C=C(N2CCCC2=O)C=1)C(O)=O.[CH:22]1([O:26][C:27]2[CH:28]=[C:29]([CH:34]=[C:35]([N:37]3[CH2:41][CH2:40][CH2:39][C:38]3=[O:42])[CH:36]=2)[C:30]([O:32]C)=[O:31])[CH2:25][CH2:24][CH2:23]1>>[CH:22]1([O:26][C:27]2[CH:28]=[C:29]([CH:34]=[C:35]([N:37]3[CH2:41][CH2:40][CH2:39][C:38]3=[O:42])[CH:36]=2)[C:30]([OH:32])=[O:31])[CH2:25][CH2:24][CH2:23]1Participants
3
Procedure
Prepared in an analogous manner to D8 from methyl 3-cyclobutyloxy-5-(2-oxopyrrolidin-1-yl)benzoate (D43).
Sources & evidence
- ORD record
- ord-6e48320c479d405d815ce3a81602fee9
- Source dataset
- uspto-grants-2006_01
- Patent number
- US06992103B2
Reaction notes
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