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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509943Generated: November 3, 2026

Potassium Carbonate → (5-Bromo-6-fluoro-pyridin-2-yl)-(2-chloro-benzyl)-amine

https://huagongshe.com/reaction/509943

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantN-bromobutanimideHCID 67184—
Reactant(2-Chloro-benzyl)-(6-fluoro-pyridin-2-yl)-amineHCID 57963158—
SolventAcetonitrileHCID 6342—
Product(5-Bromo-6-fluoro-pyridin-2-yl)-(2-chloro-benzyl)-amineHCID 5761935780%

Reaction Steps

To (2-chloro-benzyl)-(6-fluoro-pyridin-2-yl)-amine (45, 4.70 g, 19.8 mmol) in 100.0 mL of acetonitrile, N-bromosuccinimide (3.53 g, 19.8 mmol) in 20.0 mL of acetonitrile was added slowly at room temperature. The reaction was stirred at room temperature for 4 hours, then poured into aqueous potassium carbonate and extracted with ethyl acetate. The organic layer was dried over sodium sulfate, filtered and the filtrate concentrated under vacuum. The resulting material was washed with ethyl acetate in hexane to provide the desired compound (46, 5.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096593B2
Source datasetuspto-grants-2015_08
ORD IDord-f1d71c260e0d45758a7d7725d8c48425
Source noteuspto-grants-2015_08