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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 930774Generated: October 29, 2026

Potassium Carbonate → HCID 57950436, compound

https://huagongshe.com/reaction/930774

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromo-2-methoxypyridineHCID 14062309—
Reactant(2-Fluoro-4-methoxyphenyl)boronic acidHCID 15789384—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 57950436HCID 5795043657%

Reaction Conditions

Temperature90 °C

Reaction Steps

4-Bromo-2-methoxypyridine (1.39 g, 7.42 mmol), 2-fluoro-4methoxyphenylboronic acid (2.40 g, 14.1 mmol), K2CO3 (2.05 g, 14.8 mmol) and bis(triphenylphosphine) palladium(II)chloride (Pd(PPh3)2Cl2) (52 mg, 0.74 mmol) were stirred in DMSO (8.5 mL) under vacuum for 20 min. The flask was flushed with argon and the mixture was heated to 90° C. for 3 h. Upon cooling, the mixture was diluted with brine, and the aqueous solution was extracted with CH2Cl2 (3×50 mL). The combined organic extracts were washed with water (3×20 mL), dried over Na2SO4 and concentrated under reduced pressure. Flash chromatography (40+M Biotage column, CH2Cl2/(80:18:2 CH2Cl2/MeOH/NH4OH), 100:0 to 80:20) provided the title compound (0.98 g, 57%) as a yellow oil: 1H NMR (500 MHz, CDCl3) δ 8.20 (d, J=5.4 Hz, 1H), 7.42-7.38 (m, 1H), 7.07 (d, J=5.4 Hz, 1H), 6.93 (s, 1H), 6.80 (dd, J=8.6, 2.5 Hz, 1H), 6.74 (dd, J=12.6, 2.5 Hz, 1H), 3.99 (s, 3H), 3.85 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296743B2
Source datasetuspto-grants-2016_03
ORD IDord-13bf05fa388f43b5b5123486fe6ae577
Source noteuspto-grants-2016_03