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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 407915Generated: October 30, 2026

HCID 67469775, compound → HCID 67469906, compound

https://huagongshe.com/reaction/407915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67469775HCID 67469775—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 67469906HCID 6746990659.5%

Reaction Steps

Tert-butyl 4-((3S,4S)-4-(benzyloxy)-3-(2-fluoro-4-(methylsulfonyl)phenoxy)-2-oxopyrrolidin-1-yl)piperidine-1-carboxylate (160 mg, 0.284 mmol) was dissolved in EtOH (3 mL) and 100 mg 10% Pd/C was added and stirred under balloon pressure of hydrogen overnight. The reaction was filtered and concentrated to afford tert-butyl 4-((3S,4S)-3-(2-fluoro-4-(methylsulfonyl)phenoxy)-4-hydroxy-2-oxopyrrolidin-1-yl)piperidine-1-carboxylate (80 mg, 0.169 mmol, 59.5% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754226B2
Source datasetuspto-grants-2014_06
ORD IDord-957ffcc75700413ea6296c34cd83a1cc
Source noteuspto-grants-2014_06