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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827136Generated: October 30, 2026

2-Fluoropyridine → (cis)-3-Hydroxy-4-(pyridin-2-ylaminomethyl)-piperidine-1-carboxylic acid benzyl ester

https://huagongshe.com/reaction/1827136

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-FluoropyridineHCID 9746—
Reactant(cis)-4-Aminomethyl-3-hydroxy-piperidine-1-carboxylic acid benzyl esterHCID 58635348—
Product(cis)-3-Hydroxy-4-(pyridin-2-ylaminomethyl)-piperidine-1-carboxylic acid benzyl esterHCID 69415336—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of (cis)-4-aminomethyl-3-hydroxy-piperidine-1-carboxylic acid benzyl ester (0.1 g, 378 mmol) and 2-fluoropyridine (0.25 mL) was heated to 120° C. for 24 h. The reaction mixture was partitioned between EtOAc and water. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent evaporated to give a (cis)-3-hydroxy-4-(pyridin-2-ylaminomethyl)-piperidine-1-carboxylic acid benzyl ester crude product, which was purified by flash column chromatography (50% EtOAc hexane to 5% MeOH EtOAc). M.S (M+1): 342

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053089B2
Source datasetuspto-grants-2006_05
ORD IDord-72e209cb4c0948dabe69bab4fd857380
Source noteuspto-grants-2006_05