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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374309Generated: October 31, 2026

HCID 86596872, compound → HCID 86596873, compound

https://huagongshe.com/reaction/1374309

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 numberUS07163937B2
Source datasetuspto-grants-2007_01
ORD IDord-33c3cd1037db49b985dda86b2ec4fd4a
Source noteuspto-grants-2007_01