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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714906Generated: October 31, 2026

Piperidine → 5-Bromo-2-(piperidin-1-yl)pyrimidine

https://huagongshe.com/reaction/1714906

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantTriethylamineHCID 8471—
Reactant5-Bromo-2-chloropyrimidineHCID 606665—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product5-Bromo-2-(piperidin-1-yl)pyrimidineHCID 3614682—

Reaction Steps

Piperidine (5.1 ml, 51.6 mmol) was added to a stirred solution of 5-bromo-2-chloropyrimidine (5 g, 25.8 mmol) and triethylamine (9.0 ml, 64.5 mmol) in toluene (30 ml). After stirring at room temperature for 24 hours the reaction mixture was diluted with ethyl acetate and washed with 2N hydrochloric acid, brine and dried (magnesium sulfate). The organic layer was filtered, concentrated in vacuo and the resulting residue was purified by column chromatography eluting with ethyl acetate to afford the title compound (D32).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799773B2
Source datasetuspto-grants-2010_09
ORD IDord-5ff5badc1b3c48829f1fa67ec273c5da
Source noteuspto-grants-2010_09