3,5-bis(2-oxopyrrolidin-1-yl)benzoic Acid → 2-Fluoro-3,5-bis-(2-oxopyrrolidin-1-yl)benzoic Acid
Reaction equation
O=C1CCCN1C1C=C(C=C(N2CCCC2=O)C=1)C(O)=O.[F:22][C:23]1[C:32]([N:33]2[CH2:37][CH2:36][CH2:35][C:34]2=[O:38])=[CH:31][C:30]([N:39]2[CH2:43][CH2:42][CH2:41][C:40]2=[O:44])=[CH:29][C:24]=1[C:25]([O:27]C)=[O:26]>>[F:22][C:23]1[C:32]([N:33]2[CH2:37][CH2:36][CH2:35][C:34]2=[O:38])=[CH:31][C:30]([N:39]2[CH2:43][CH2:42][CH2:41][C:40]2=[O:44])=[CH:29][C:24]=1[C:25]([OH:27])=[O:26]Participants
3
Procedure
Prepared in an analogous manner to D8 from methyl 2-fluoro-3,5-bis-(2-oxopyrrolidin-1-yl)benzoate (D39).
Sources & evidence
- ORD record
- ord-573bd6c6b02f4cc99760d9b06b8db401
- Source dataset
- uspto-grants-2006_01
- Patent number
- US06992103B2
Reaction notes
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