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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712720Generated: October 31, 2026

(R)-3-(5-bromo-pyridin-3-yloxy)-piperidine-1-carboxylic acid tert-butyl ester → 3-bromo-5-((R)-piperidin-3-yloxy)-pyridine

https://huagongshe.com/reaction/712720

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-3-(5-bromo-pyridin-3-yloxy)-piperidine-1-carboxylic acid tert-butyl esterHCID 117667237—
SolventHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
Solvent1,4-DioxaneHCID 31275—
Product3-bromo-5-((R)-piperidin-3-yloxy)-pyridineHCID 117667565120.1%

Reaction Steps

A solution of (R)-3-(5-bromo-pyridin-3-yloxy)-piperidine-1-carboxylic acid tert-butyl ester (596 mg, 1.7 mmol) in MeOH (5 mL) and HCl solution in 1,4-dioxane (4N; 1.5 mL) is stirred at room temperature for 16 h. The mixture is concentrated to provide 525 mg 3-bromo-5-((R)-piperidin-3-yloxy)-pyridine as the hydrochloride salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181272B2
Source datasetuspto-grants-2015_11
ORD IDord-8237b17ba3c44a49b679c8846484354f
Source noteuspto-grants-2015_11