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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695715Generated: November 2, 2026

Pyridine → N-(5-Bromo-2-chloropyridin-3-yl)benzenesulfonamide

https://huagongshe.com/reaction/1695715

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBenzenesulfonyl chlorideHCID 7369—
Reactant3-Amino-5-bromo-2-chloropyridineHCID 21858354—
SolventDichloromethaneHCID 6344—
ProductN-(5-Bromo-2-chloropyridin-3-yl)benzenesulfonamideHCID 57843322—

Reaction Steps

Benzenesulfonyl chloride (2.24 ml, 17.5 mmol) was added dropwise over 5-10 mins to a solution of 5-bromo-2-chloro-3-pyridinamine (2.5 g, 12.1 mmol) and pyridine (1.5 ml, 18.56 mmol) in DCM (25 ml). The reaction was stirred for 18 h at RT before evaporation to dryness in vacuo. The residue was split in two and purified by silica gel chromatography, eluting with 0-100% DCM in cyclohexane. Appropriate fractions were combined and evaporated to give title compound, 1.81 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163743B2
Source datasetuspto-grants-2012_04
ORD IDord-e8842bfc8421442392d6bb583758f8ed
Source noteuspto-grants-2012_04