(S)-1-Cbz-3-Aminopyrrolidine → HCID 67346798, compound

HRID 1670028Notes

Reaction equation

HRID 1670028 reaction equation
C(N1CC[C@H](N)C1)(OCC1C=CC=CC=1)=O.C([N:24]1[CH2:29][CH2:28][CH:27]([N:30]([CH:38]2[CH2:43][CH2:42][CH2:41][CH2:40][CH2:39]2)[C:31](=[O:37])[N:32]([CH3:36])[CH:33]([CH3:35])[CH3:34])[CH2:26][CH2:25]1)(OC(C)(C)C)=O>>[CH:38]1([N:30]([C:31](=[O:37])[N:32]([CH3:36])[CH:33]([CH3:34])[CH3:35])[CH:27]2[CH2:28][CH2:29][NH:24][CH2:25][CH2:26]2)[CH2:43][CH2:42][CH2:41][CH2:40][CH2:39]1

Participants

3

Reactant 2

HCID 1519355(S)-1-Cbz-3-AminopyrrolidineHCID 67345624HCID 67345624, compound

Product 1

HCID 67346798HCID 67346798, compound

Procedure

The title compound was prepared following the procedure described in Step B of Intermediate 1 using 1-BOC-4-{cyclohexyl[methyl(isopropyl)carbamoyl]amino}piperidine.

Sources & evidence

ORD record
ord-d1a859f5ba5b4de7a962a823cbab0052
Source dataset
uspto-grants-2011_08
Patent number
US07989634B2

Reaction notes

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