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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500266Generated: October 30, 2026

Potassium Carbonate → 4-(2-Aminopyrimidin-5-yl)-2,3-difluorobenzoic acid

https://huagongshe.com/reaction/500266

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Amino-5-bromopyrimidineHCID 231310—
Reactant4-Borono-2,3-difluorobenzoic acidHCID 53216746—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product4-(2-Aminopyrimidin-5-yl)-2,3-difluorobenzoic acidHCID 67225257—

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 4-(dihydroxyboryl)-2,3-difluorobenzoic acid (0.47 g, 2.3 mmol), 5-bromopyrimidin-2-amine (0.44 g, 2.6 mmol), tetrakis(triphenylphosphine)palladium (0.1 g, 0.1 mmol), and potassium carbonate (0.96 g, 7.0 mmol) in toluene (4.0 mL), ethanol (2.0 mL) and water (2.0 mL) was heated at 110° C. for 3 h. After cooling to RT, the mixture was washed with ether to remove impurity. The aqueous layer was adjusted to pH 6 with 1N HCl. The solid was filtered, washed with water and ether to give the desired product. LCMS: (M+H)=252.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767675B2
Source datasetuspto-grants-2010_08
ORD IDord-b90257f63da64419a42d9344cc5dc379
Source noteuspto-grants-2010_08