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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850763Generated: October 31, 2026

benzyl 4-((1R,2S)-2-{2-[4-(2-azetidin-1-yl-2-oxoethyl)-3-fluorophenoxy]ethyl}cyclopropyl)piperidine-1-carboxylate → 4-((1R,2S)-2-{2-[4-(2-azetidin-1-yl-2-oxoethyl)-3-fluorophenoxy]ethyl)cyclopropyl)piperidine

https://huagongshe.com/reaction/1850763

Reaction equation

Participants

RoleNameHCIDCharge
Reactantbenzyl 4-((1R,2S)-2-{2-[4-(2-azetidin-1-yl-2-oxoethyl)-3-fluorophenoxy]ethyl}cyclopropyl)piperidine-1-carboxylateHCID 70856384—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product4-((1R,2S)-2-{2-[4-(2-azetidin-1-yl-2-oxoethyl)-3-fluorophenoxy]ethyl)cyclopropyl)piperidineHCID 70856322—

Reaction Steps

To a solution of benzyl 4-((1R,2S)-2-{2-[4-(2-azetidin-1-yl-2-oxoethyl)-3-fluorophenoxy]ethyl}cyclopropyl)piperidine-1-carboxylate (590 mg, 1.32 mmol) in 8 mL anhydrous methanol at ambient temperature was added palladium on carbon (80.0 mg, 0.676 mmol), 10% by weight. The solution was stirred under hydrogen for 4 hours and filtered. The crude product was concentrated to the title compound as white solid and used for the next step. LC/MS 361.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957062B2
Source datasetuspto-grants-2015_02
ORD IDord-497cbb93515a41bcaf5691d23df2d035
Source noteuspto-grants-2015_02