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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754728Generated: October 28, 2026

Water → (5-Bromo-6-chloro-pyridin-2-yl)-(4-chloro-benzyl)-amine

https://huagongshe.com/reaction/1754728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-bromobutanimideHCID 67184—
Reactant(4-Chloro-benzyl)-(6-chloro-pyridin-2-yl)-amineHCID 57619237—
SolventAcetonitrileHCID 6342—
Product(5-Bromo-6-chloro-pyridin-2-yl)-(4-chloro-benzyl)-amineHCID 57619309—

Reaction Steps

To (4-chloro-benzyl)-(6-chloro-pyridin-2-yl)-amine (538, 4.00 g, 0.0158 mol) in acetonitrile (66.7 mL, 1.28 mol) under an atmosphere of nitrogen, N-bromosuccinimide (2.81 g, 0.0158 mol) in acetonitrile (20 mL) was added slowly. The reaction was stirred at room temperature overnight, then poured into water and extracted with ethyl acetate. The organic layer was dried over sodium sulfate, concentrated and crystallized with ethyl acetate in hexane to give a white solid (539, 2.60 g, 95.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169250B2
Source datasetuspto-grants-2015_10
ORD IDord-15f917479d7a4133b04098b042ae33c6
Source noteuspto-grants-2015_10