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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1970264Generated: November 3, 2026

Potassium Carbonate → HCID 59272394, compound

https://huagongshe.com/reaction/1970264

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(Pyrimidin-5-yl)boronic acidHCID 2795193—
Reactant5-bromo-2-(2-chloropyridin-4-yloxy)-N,N-diethylbenzamideHCID 59272340—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59272394HCID 59272394—

Reaction Conditions

Temperature100 °C

Reaction Steps

A resealable tube was charged with a mixture of 5-bromo-2-(2-chloropyridin-4-yloxy)-N,N-diethylbenzamide (2.500 g, 6.52 mmol), pyrimidin-5-ylboronic acid (2.018 g, 16.29 mmol), and potassium carbonate (4.50 g, 32.6 mmol) in THF (40.0 mL) and water (10.0 mL). Tetrakis(triphenylphosphine)palladium(0) (0.376 g, 0.326 mmol) was added, the system was purged with argon, and the tube was sealed. The reaction mixture was stirred at 100° C. for 4.0 h. The reaction mixture was partitioned between EtOAc and water. The aqueous phase was separated and extracted with EtOAc. The combined organic phases were washed with brine, dried over anhydrous sodium sulfate, filtered, and concentrated to afford a brown solid. This material was purified via column chromatography on silica gel (RediSep 120 g column, gradient elution with 50-100% ethyl acetate-hexane) to afford 2-(2-chloropyridin-4-yloxy)-N,N-diethyl-5-(pyrimidin-5-yl)benzamide as an off-white solid. MS m/z=383.2 [M+H]+. Calcd for C20H19ClN4O2: 382.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426447B2
Source datasetuspto-grants-2013_04
ORD IDord-f3341cb24bf64af9b55f889e66c1297d
Source noteuspto-grants-2013_04