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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850772Generated: October 30, 2026

benzyl 4-((1R,2S)-2-(2-(5-(methylsulfonyl)pyridin-2-yloxy)ethyl)cyclopropyl)piperidine-1-carboxylate → 5-(methylsulfonyl)-2-{2-[(1S,2R)-2-piperidin-4-ylcyclopropyl]ethoxy}pyridine

https://huagongshe.com/reaction/1850772

Reaction equation

Participants

RoleNameHCIDCharge
Reactantbenzyl 4-((1R,2S)-2-(2-(5-(methylsulfonyl)pyridin-2-yloxy)ethyl)cyclopropyl)piperidine-1-carboxylateHCID 70819038—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product5-(methylsulfonyl)-2-{2-[(1S,2R)-2-piperidin-4-ylcyclopropyl]ethoxy}pyridineHCID 70819227—

Reaction Steps

To a solution of 1.16 g (2.53 mmol) benzyl 4-[(1R,2S)-2-(2-{[5-(methylsulfonyl)pyridin-2-yl]oxy}ethyl)cyclopropyl]piperidine-1-carboxylate in 15 ml anhydrous methanol at ambient temperature was added 0.12 g (1.13 mmol) palladium on carbon, 10% by weight. The solution was stirred under hydrogen for 4 hours and filtered. The crude product was concentrated to give the title compound as white solid and used for the next step. LC/MS 325.5 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957062B2
Source datasetuspto-grants-2015_02
ORD IDord-2ce0301331a9452da0a24cc31f5d4d70
Source noteuspto-grants-2015_02