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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1367360Generated: October 30, 2026

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

https://huagongshe.com/reaction/1367360

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 numberUS07893075B2
Source datasetuspto-grants-2011_02
ORD IDord-bf0341f0524f49d7bc9e557a84fa3f35
Source noteuspto-grants-2011_02