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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1410405Generated: November 2, 2026

Sodium Carbonate → HCID 57584405, compound

https://huagongshe.com/reaction/1410405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4,6-DichloropyrimidineHCID 70943—
Reactant(Naphthalen-2-yl)boronic acidHCID 2734375—
CatalystHCID 178418476HCID 178418476—
CatalystHCID 178419050HCID 178419050—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 57584405HCID 5758440548%

Reaction Steps

First, into a recovery flask equipped with a reflux pipe were put 5.0 g of 4,6-dichloropyrimidine, 11.7 g of 2-naphthaleneboronic acid, 7.2 g of sodium carbonate, 0.29 g of bis(triphenylphosphine)palladium (II) dichloride (abbreviation: Pd(PPh3)2Cl2), 20 mL of water, and 20 mL of acetonitrile, and the air in the flask was replaced with argon. This reaction container was heated by irradiation with microwaves (2.45 GHz, 100 W) for 60 minutes. Here, into the flask were further put 2.9 g of 2-naphthaleneboronic acid, 1.8 g of sodium carbonate, 0.070 g of Pd(PPh3)2Cl2, 5 mL of water, and 5 mL of acetonitrile, and the mixture was heated again by irradiation with microwaves (2.45 GHz, 100 W) for 60 minutes. After that, water was added to this solution and an organic layer was extracted with dichloromethane. The obtained organic layer was washed with water and dried with magnesium sulfate. The solution after drying was filtered. The solvent of this solution was distilled off, and then the obtained residue was purified by silica gel column chromatography using hexane and ethyl acetate as a developing solvent in a ratio of 5:1, so that a pyrimidine derivative 4-chloro-6-(naphthalen-2-yl)pyrimidine was obtained (yellow white powder, yield of 48%). Note that the irradiation with microwaves was performed using a microwave synthesis system (Discover, manufactured by CEM Corporation). A synthesis scheme (s-1) of Step 1 is shown below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921548B2
Source datasetuspto-grants-2014_12
ORD IDord-3df0c318de424878b90ca6cae261c241
Source noteuspto-grants-2014_12