(S)-1-Cbz-3-Aminopyrrolidine → HCID 86050991, compound
Reaction equation
C(N1CC[C@H](N)C1)(OCC1C=CC=CC=1)=O.[CH3:17][O:18][C:19](=[O:41])[CH2:20][N:21]([CH:35]1[CH2:40][CH2:39][CH2:38][CH2:37][CH2:36]1)[CH:22]1[CH2:27][CH2:26][N:25](C(OC(C)(C)C)=O)[CH2:24][CH2:23]1>>[CH3:17][O:18][C:19](=[O:41])[CH2:20][N:21]([CH:35]1[CH2:40][CH2:39][CH2:38][CH2:37][CH2:36]1)[CH:22]1[CH2:23][CH2:24][NH:25][CH2:26][CH2:27]1Participants
3
Procedure
The title compound was prepared following the procedure described in Step B of Intermediate 1 using methyl{cyclohexyl[1-(BOC)piperidin-4-yl]amino}acetate prepared in Step A.
Sources & evidence
- ORD record
- ord-23a949e87900401db8981570b50ac75b
- Source dataset
- uspto-grants-2011_08
- Patent number
- US07989634B2
Reaction notes
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