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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192335Generated: November 1, 2026

Triethylamine → 2-bromo-N-pyridin-2-yl-acetamide

https://huagongshe.com/reaction/2192335

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-AminopyridineHCID 10439—
ReactantBromoacetyl bromideHCID 61147—
SolventTetrahydrofuranHCID 8028—
Product2-bromo-N-pyridin-2-yl-acetamideHCID 3415837—

Reaction Steps

To a solution of 2-aminopyridine (48.8 mmol) in anhydrous THF (98 mL) at room temperature was added Et3N (58.6 mmol) and bromoacetyl bromide (58.6 mmol) dropwise The mixture was stirred overnight and quenched with sat. NaHCO3 (aq). EtOAc was added to the mixture and the layers separated. The aqueous phase was extracted with EtOAc and the combined organics dried (MgSO4) and concentrated in vacuo to a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329729B2
Source datasetuspto-grants-2012_12
ORD IDord-6549214e493a46aa947896b6d4871768
Source noteuspto-grants-2012_12