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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397703Generated: October 30, 2026

tert-butyl (2S)-2-[(Z)-N'-[(2R)-2-phenyl-2-(phenylmethoxycarbonylamino)acetyl]oxycarbamimidoyl]piperidine-1-carboxylate → tert-butyl (2S)-2-{5-[(R)-{[(benzyloxy)carbonyl]amino}(phenyl)methyl]-1,2,4-oxadiazol-3-yl}-1-piperidinecarboxylate

https://huagongshe.com/reaction/397703

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl (2S)-2-[(Z)-N'-[(2R)-2-phenyl-2-(phenylmethoxycarbonylamino)acetyl]oxycarbamimidoyl]piperidine-1-carboxylateHCID 59085900—
SolventPyridineHCID 1049—
Producttert-butyl (2S)-2-{5-[(R)-{[(benzyloxy)carbonyl]amino}(phenyl)methyl]-1,2,4-oxadiazol-3-yl}-1-piperidinecarboxylateHCID 57119964—

Reaction Steps

The title compound was prepared by a similar method to Preparation 6 from tert-butyl (2S)-2-[(Z,5R)-1-amino-4,7-dioxo-5,9-diphenyl-3,8-dioxa-2,6-diaza-1-nonen-1-yl]-1-piperidinecarboxylate [see Preparation 10 1] and pyridine to afford tert-butyl (2S)-2-{5-[(R)-{[(benzyloxy)carbonyl]amino}(phenyl)methyl]-1,2,4-oxadiazol-3-yl}-1-piperidinecarboxylate as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610707B1
Source datasetuspto-grants-2003_08
ORD IDord-1d6f39fc62df461b97e6a19abf767629
Source noteuspto-grants-2003_08