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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419512Generated: November 1, 2026

Potassium Carbonate → HCID 59452704, compound

https://huagongshe.com/reaction/419512

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(Pyridin-4-yl)boronic acidHCID 2734379—
Reactant4-Bromo-2-ethoxy-1-nitrobenzeneHCID 15555501—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventDimethylacetamideHCID 31374—
ProductHCID 59452704HCID 5945270455.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 5-bromo-2-nitrophenyl ethyl ether (Example 146, step A) (4.5 g, 18.3 mmol), PdCl2(dppf)*DCM (1.34 g, 1.82 mmol) and 4-pyridylboronic acid (4.5 g, 36.6 mmol) in N,N-dimethylacetamide (110 mL) was deoxygenated by bubbling with N2 (g) for ca 15 min. To this solution was added degassed 1.6 N K2CO3 (aq) (55 mL, 6.0 equiv.) and the resulting slurry was warmed to 80° C. for 24 h. The N,N-dimethylacetamide was removed under reduced pressure and the solids were taken up in EtOAc, filtered to remove insoluble solids, washed with H2O, and dried (Na2SO4). The solvent was rotovaped down and the crude product was purified by flash chromatography to give the title compound of step A (2.46 g, 10.1 mmol, 55%). 1H NMR (400 MHz, CDCl3) δ ppm 8.72 (dd, J=4.67, 1.56 Hz, 2H), 7.93 (d, J=8.06 Hz, 1H), 7.45-7.51 (m, 2H), 7.21-7.26 (m, 2H), 4.26 (q, J=6.96 Hz, 2H), 1.51 (t, J=6.96 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093239B2
Source datasetuspto-grants-2012_01
ORD IDord-a4a9cc9d4cdf4f5ca84109a3ea3d63e7
Source noteuspto-grants-2012_01