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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1811712Generated: November 2, 2026

Water → HCID 59224651, compound

https://huagongshe.com/reaction/1811712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-Amino-4,6-dichloropyrimidineHCID 65522—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 59224645HCID 59224645—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 59224651HCID 5922465165.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

2-Amino-4,6-dichloropyrimidine (246 mg, 1.5 mmol), bis(triphenylphosphine) palladium dichloride (53 mg, 0.07 mmol), sodium bicarbonate (252 mg, 3.0 mmol), 1,4-dioxane (2.5 ml), and water (1.5 ml) were placed in a reaction vessel. The resulting mixture was stirred at 80° C. for 10 minutes. To this mixture, 2-Ethoxy-4-methyl-5-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)benzoic acid methyl ester (320 mg, 1.0 mmol) obtained in Step 4 above was added dropwise after dissolving in 1,4-dioxane (2.5 ml). The resulting mixture was stirred at 80° C. for 20 hours. The reaction solution was diluted with ethyl acetate (100 ml), and washed three times with water (40 ml), and then with a saturated aqueous sodium chloride solution (40 ml). The washed ethyl acetate solution was dried over anhydrous sodium sulfate (10 g). After filtration, the filtrate was concentrated under reduced pressure. The resulting crude product was purified by silica gel column chromatography (developing solvent: n-hexane:ethyl acetate=2:1) to yield 5-(2-amino-6-chloropyrimidin-4-yl)-2-ethoxy-4-methylbenzoic acid methyl ester (Compound 1-3) (210 mg) as a yellow solid material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362236B2
Source datasetuspto-grants-2013_01
ORD IDord-8ec7ec39009d4bae8a17115e650baecd
Source noteuspto-grants-2013_01