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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171540Generated: November 1, 2026

HCID 86596872, compound → HCID 86596873, compound

https://huagongshe.com/reaction/1171540

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 numberUS07829571B2
Source datasetuspto-grants-2010_11
ORD IDord-d1db827f080c45c4b92f66230b745199
Source noteuspto-grants-2010_11