1,2-Pyrrolidinedicarboxylic acid, 1-(1,1-dimethylethyl) ester, (2S)- → Pyrrolidine-1,2-dicarboxylic acid
Reaction equation
C(OC(N1C(C(O)C(O)C)CNC2NC(N=CN(C)C)=NC(=O)C1=2)=O)(C)(C)C.[C:29]([N:36]1[CH2:43][CH2:42][CH2:41][C@H:37]1[C:38]([OH:40])=[O:39])([O:31]C(C)(C)C)=[O:30]>>[N:36]1([C:29]([OH:31])=[O:30])[CH2:43][CH2:42][CH2:41][CH:37]1[C:38]([OH:40])=[O:39]Participants
3
Procedure
The product of Example 5, step b) was treated by the same method as that described in Example 10, step a) except N-Boc-L-Proline (12.6 g, 5.87 mmol) was used to give the sub-title compound as a pale yellow solid (3.0 g, 60%). MS: ESI (positive): 791 (M+H).
Sources & evidence
- ORD record
- ord-c8ba5ea9e3204ee78dc2a52a6b18696e
- Source dataset
- uspto-grants-2012_12
- Patent number
- US08324210B2
Reaction notes
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