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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 646165Generated: October 30, 2026

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

https://huagongshe.com/reaction/646165

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantHCID 86593682HCID 86593682—
SolventDimethylformamideHCID 6228—
Product5-Bromo-2-(piperidin-1-yl)pyridineHCID 16414209—

Reaction Conditions

Temperature40 °C

Reaction Steps

A mixture of trifluoromethanesulfonic acid 5-bromopyrid-2-yl ester (see step (a) above; 1.5 g, 4.9 mmol), piperidine (1.07 mL, 10.8 mmol) and DMF (5 mL) was heated at 40° C. for 3 h. DMF was then removed in vacuo, water (20 mL) was added to the residue and the product extracted with EtOAc (3×15 mL) and CH2Cl2 (15 mL). The combined organic extracts were washed with brine and dried (Na2SO4). After removal of the solvent, the residue was dissolved in Et2O and HCl (4M in dioxane; 4 mL) was added.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07705023B2
Source datasetuspto-grants-2010_04
ORD IDord-5e18a207fb984b58bcb0ac15508d974d
Source noteuspto-grants-2010_04