(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]1

Participants

Reactant 2

HCID 1519355(S)-1-Cbz-3-Aminopyrrolidine

HCID 131729086HCID 131729086, compound

Product 1

HCID 86050991HCID 86050991, compound

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
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07989634B2

Reaction notes

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