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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1024190Generated: October 23, 2026

Hydrochloric Acid → 5-Bromo-pyridine-2-carboxylic acid (4-chloro-phenyl)-amide

https://huagongshe.com/en/reaction/1024190

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyridineHCID 1049—
Reactant4-ChloroanilineHCID 7812—
Reactant5-Bromo-pyridine-2-carbonyl chlorideHCID 19090771—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product5-Bromo-pyridine-2-carboxylic acid (4-chloro-phenyl)-amideHCID 59593371—

Reaction Conditions

Temperature68 °C

Reaction Steps

To 5-Bromo-pyridine-2-carbonyl chloride (69, 0.76 g, 3.4 mmol) in acetonitrile (29.0 mL) were added p-chloroaniline (53, 0.702 g, 5.50 mmol), 4-dimethylamino-pyridine (0.12 g, 0.96 mmol) and pyridine (2.9 mL, 0.036 mol). The reaction was stirred at 68° C. overnight, then poured into water, acidified with 1N HCl to pH around 1 and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated and purified by silica gel column chromatography eluting with dichloromethane to give a white solid (70, 0.75 g, 70.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722702B2
Source datasetuspto-grants-2014_05
ORD IDord-8d55364b25e644b4a76c53b27d8e02a8
Source noteuspto-grants-2014_05