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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455405Generated: November 1, 2026

HCID 86596872, compound → HCID 86596873, compound

https://huagongshe.com/reaction/1455405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86596872HCID 86596872—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 86596873HCID 8659687353%

Reaction Steps

Tert-butyl (1R,3R,4S)-4-((S)-3-benzyloxycarbonylamino-2-oxopyrrolidin-1-yl)-3-(phenylthiomethyl)cyclohexylcarbamate (150 mg) was dissolved in EtOH (2 mL) prior to the addition of Raney 2800 nickel (100 mg) in water. The reaction was heated at reflux for 12 h. After cooling to rt, the reaction was concentrated. The resulting residue was purified by flash chromatography to afford tert-butyl (1R,3R,4S)-4-((S)-3-benzyloxycarbonylamino-2-oxopyrrolidin-1-yl)-3-methylcyclohexylcarbamate (64 mg). MS found: (M+H)+=446.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07482335B2
Source datasetuspto-grants-2009_01
ORD IDord-e97d539a66f24ca7b9bae06bc5383fc4
Source noteuspto-grants-2009_01