Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1970263Generated: November 3, 2026

Cesium carbonate → 5-bromo-2-(2-chloropyridin-4-yloxy)-N,N-diethylbenzamide

https://huagongshe.com/reaction/1970263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant2-Chloro-4-fluoropyridineHCID 2782792—
Reactant5-bromo-N,N-diethyl-2-hydroxybenzamideHCID 24285295—
SolventAcetonitrileHCID 6342—
Product5-bromo-2-(2-chloropyridin-4-yloxy)-N,N-diethylbenzamideHCID 59272340—

Reaction Conditions

Temperature100 °C

Reaction Steps

2-Chloro-4-fluoropyridine (0.242 g, 1.837 mmol) was added to a mixture of 5-bromo-N,N-diethyl-2-hydroxybenzamide (0.500 g, 1.837 mmol) and cesium carbonate (1.197 g, 3.67 mmol) in acetonitrile (10.0 mL). The mixture stirred at 100° C. for 8 h. The reaction mixture was partitioned between ethyl acetate and water. The aqueous phase was separated and extracted with ethyl acetate. The combined organic phases were washed with brine, dried over anhydrous sodium sulfate, filtered, and concentrated to afford a brown oil. This oil was purified via column chromatography on silica gel (RediSep 80 g column, gradient elution with 0-50% ethyl acetate-hexane) to afford 5-bromo-2-(2-chloropyridin-4-yloxy)-N,N-diethylbenzamide as a thick, yellow oil. MS m/z=383.0 [M+H]+. Calcd for C16H16BrClN2O2: 382.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426447B2
Source datasetuspto-grants-2013_04
ORD IDord-360d46d15d2f40c3af7464f922160faa
Source noteuspto-grants-2013_04