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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754723Generated: October 28, 2026

Sodium Thiosulfate → (5-Bromo-6-fluoro-pyridin-2-yl)-(4-chloro-benzyl)-amine

https://huagongshe.com/reaction/1754723

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantN-bromobutanimideHCID 67184—
Reactant(4-Chloro-benzyl)-(6-fluoro-pyridin-2-yl)-amineHCID 57619459—
SolventAcetonitrileHCID 6342—
Product(5-Bromo-6-fluoro-pyridin-2-yl)-(4-chloro-benzyl)-amineHCID 57619198—

Reaction Steps

To (4-chloro-benzyl)-(6-fluoro-pyridin-2-yl)-amine (536, 1.03 g, 4.35 mmol) in acetonitrile (30.0 mL), under an atmosphere of nitrogen, N-bromosuccinimide (0.820 g, 4.61 mol) was added slowly. After 2 hours, the reaction was poured into a solution of sodium thiosulfate and extracted with ethyl acetate. The organic layer was dried over sodium sulfate, concentrated and crystallized with ethyl acetate and hexane to give a white solid (537, 1.10 g, 80.1%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169250B2
Source datasetuspto-grants-2015_10
ORD IDord-abe304a3b3f140989f89c4b7d77806c0
Source noteuspto-grants-2015_10