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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tributylamine | HCID 7622 | — |
| Reactant | 2-Chloro-1-methylpyridinium iodide | HCID 167069 | — |
| Reactant | 3-Amino-5-bromopyridine | HCID 817681 | — |
| Reactant | 3-(Dimethylamino)propanoic acid hydrochloride | HCID 11586327 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(5-Bromo-pyridin-3-yl)-3-dimethylamino-propionamide | HCID 68763057 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08314112B2 |
|---|
| Source dataset | uspto-grants-2012_11 |
|---|
| ORD ID | ord-3d2afb53c695440d9e8d8c8949714e63 |
|---|
| Source note | uspto-grants-2012_11 |
|---|