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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 626897Generated: October 25, 2026

Sodium Carbonate → 2-Chloro-4-(5-ethoxy-2-fluoro-phenyl)-6-methyl-pyrimidine

https://huagongshe.com/reaction/626897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2,4-Dichloro-6-methylpyrimidineHCID 79471—
Reactant5-Ethoxy-2-fluorophenylboronic Acid (contains varying amounts of Anhydride)HCID 16217468—
CatalystHCID 178419050HCID 178419050—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2-Chloro-4-(5-ethoxy-2-fluoro-phenyl)-6-methyl-pyrimidineHCID 9001539296.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 2,4-dichloro-6-methyl-pyrimidine (2.66 g, 16.31 mmol) and (5-ethoxy-2-fluoro-phenyl)boronic acid (2 g, 10.87 mmol) in 1,2-dimethoxyethane (25 mL) and water (15 mL) was added sodium carbonate (3.46 g, 32.62 mmol). This was degassed with nitrogen for 5 minutes. Bis(triphenylphosphine)palladium (II) dichloride (0.38 g, 0.54 mmol) was then added and the reaction was heated to 80° C. overnight. The solvent was evaporated and the residue was partitioned between water (300 mL) and EtOAc (300 mL). The organics were washed with brine (100 mL), dried over MgSO4 and concentrated in vacuo to afford a yellow oil. The material was purified using a Biotage SP4 eluting with 0 to 30% i-hexane/EtOAc and the product containing fractions were collected and the solvent evaporated to give a colourless solid (2.8 g) mainly 2-chloro-4-(5-ethoxy-2-fluoro-phenyl)-6-methyl-pyrimidine (D16)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309254B2
Source datasetuspto-grants-2016_04
ORD IDord-43e6a028560a4eb59ea6b00184185984
Source noteuspto-grants-2016_04