Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709816Generated: October 31, 2026

Sodium Carbonate → HCID 117760267, compound

https://huagongshe.com/reaction/709816

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-Fluoro-5-methoxyphenylboronic acidHCID 4157211—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
ReactantHCID 117760014HCID 117760014—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
ProductHCID 117760267HCID 11776026793.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

Under an argon atmosphere, to a solution of methyl 5-bromo-4-isobutoxypyrimidine-2-carbonitrile (1.71 g) in toluene (20 mL) were added 2-fluoro-5-methoxyphenylboronic acid (1.70 g), tris(dibenzylideneacetone)dipalladium(0) (245 mg), 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (439 mg) and 2.0 M aqueous sodium carbonate solution (10.0 mL), and the mixture was stirred at 80° C. for 1 hr. The reaction mixture was filtered through celite, and water was added at room temperature. The reaction mixture was extracted with ethyl acetate, and the extract was washed with water and saturated brine. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (1.78 g) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181186B2
Source datasetuspto-grants-2015_11
ORD IDord-c16a2aac1054416e9aff2d683eda835c
Source noteuspto-grants-2015_11