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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1878616Generated: October 26, 2026

Tributylamine → N-(5-Bromo-pyridin-3-yl)-3-dimethylamino-propionamide

https://huagongshe.com/reaction/1878616

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylamineHCID 7622—
Reactant2-Chloro-1-methylpyridinium iodideHCID 167069—
Reactant3-Amino-5-bromopyridineHCID 817681—
Reactant3-(Dimethylamino)propanoic acid hydrochlorideHCID 11586327—
SolventDichloromethaneHCID 6344—
ProductN-(5-Bromo-pyridin-3-yl)-3-dimethylamino-propionamideHCID 68763057—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 3-amino-5-bromopyridine (Sigma-Aldrich, St. Louis, USA) (1 eq, 11.2 mmol, 2.00 g) and 3-dimethylaminopropionic acid hydrochloride (ABCR GmbH & Co. KG, Karlsruhe, Germany) (1 eq, 11.2 mmol, 1.74 g) in DCM (50 ml), tributylamine (3.6 eq, 40.4 mmol, 9.8 ml) and 2-chloro-1-methylpyridinium iodide (1.2 eq, 13.5 mmol, 3.54 g) are added. The resulting mixture is heated at 50° C. for 4 h, then the solvents are removed in vacuo, aqueous NaOH solution (1 M) is added, and the mixture is extracted with DCM. The organic layer is dried with MgSO4, filtered, and the solvent is removed in vacuo. Purification by column chromatography (DCM/MeOH) yields the title compound; [M+H]+=273.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314112B2
Source datasetuspto-grants-2012_11
ORD IDord-3d2afb53c695440d9e8d8c8949714e63
Source noteuspto-grants-2012_11