Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 988105Generated: November 2, 2026

4-Bromopyridinium chloride → HCID 18007557, compound

https://huagongshe.com/reaction/988105

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromopyridinium chlorideHCID 88100—
ReactantHCID 18007542HCID 18007542—
SolventTolueneHCID 1140—
ProductHCID 18007557HCID 1800755722.9%

Reaction Steps

A solution of 1-(2-(N,N-dimethylamino)ethyl)-6-tributylstannyl-1H-indazole (49.1 mg, 0.10 mmol), 4-bromopyridine hydrochloride (21.6 mg, 0.11 mmol), tetrakistriphenylphosphine palladium(0) (10-20 mg, catalytic) in toluene (0.5 mL) was heated at reflux under an inert atmosphere for 18 h. After cooling to room temperature the reaction was quenched by the addition of aqueous sodium hydroxide (1 M, 2 mL) and water (10 mL), and the product extracted into ethyl acetate (50 mL). The organic layer was washed sequentially with water and brine, dried over sodium sulfate and the solvent removed in vacuo. Filtration through an SPE cartridge (Supelco, 6 mL, silica gel, 1000 mg, gradient from 0-10% 2M methanolic ammonia in dichloromethane) gave a crude product which was further purified by flash chromatography (silica gel, 4-10% 2M methanolic ammonia in dichloromethane) to give the title product (6.1 mg, 11%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06635639B2
Source datasetuspto-grants-2003_10
ORD IDord-96055a541edb486ebdc5ff38509e9dc6
Source noteuspto-grants-2003_10