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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 245280Generated: October 25, 2026

4-Chloro-2-fluoro-3-methoxyphenylboronic acid → 6-Amino-2-(4-chloro-2-fluoro-3-methoxyphenyl)pyrimidine-4-carboxylic acid methyl ester

https://huagongshe.com/reaction/245280

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-2-fluoro-3-methoxyphenylboronic acidHCID 44129706—
ReactantMethyl 6-amino-2-chloropyrimidine-4-carboxylateHCID 53396493—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product6-Amino-2-(4-chloro-2-fluoro-3-methoxyphenyl)pyrimidine-4-carboxylic acid methyl esterHCID 5943208353.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

6-Amino-2-chloropyrimidine-4-carboxylic acid methyl ester (2.25 g, 12 mmol, 4-chloro-2-fluoro-3-methoxyphenylboronic acid (3.27 g, 16 mmol), and bis(triphenylphosphine)palladium(II) dichloride (842 mg, 1.2 mmol) were combined in 12 mL of 1,2-dimethoxyethane and 12 mL of water. The reaction mixture was heated at 80° C. for 2 h and the cooled reaction mixture was partitioned between ethyl acetate and water. The organic phase was washed with water, dried, and concentrated under vacuum. The product was purified by flash chromatography on silica gel to yield the title compound (2.0 g, 53.5% yield): mp 188-190° C.: 1H NMR (CDCl3) δ 7.66 (dd, 1H), 7.22 (dd, 1H), 7.14 (s, 1H), 5.25 (br s, 2H), 4.0 (s, 3H), 3.99 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658791B2
Source datasetuspto-grants-2014_02
ORD IDord-8cbee6570fb84ca3b9e972863db6d1d8
Source noteuspto-grants-2014_02