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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1778172Generated: November 1, 2026

Cesium carbonate → 5-(2,6-Dichloropyrimidin-4-yl)-3-(trifluoromethyl)pyridin-2-amine

https://huagongshe.com/reaction/1778172

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant2,4,6-TrichloropyrimidineHCID 77378—
Reactant5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-3-(trifluoromethyl)pyridin-2-amineHCID 46864103—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventAcetonitrile--water (1/1)HCID 18373917—
Product5-(2,6-Dichloropyrimidin-4-yl)-3-(trifluoromethyl)pyridin-2-amineHCID 11767809159.3%

Reaction Steps

To a microwave vial charged with 2,4,6-trichloropyrimidine (300 mg, 1.64 mmol), 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-(trifluoromethyl)pyridin-2-amine (518 mg, 1.80 mmol) and cesium carbonate (1.07 g, 3.27 mmol) in acetonitrile/water (4:1, 30 mL) was added 1,1′-bis(diphenylphosphino)ferrocene-palladium(II)dichloride (60 mg, 0.05 mmol) under nitrogen. The mixture was stirred at room temperature for 16 h. The reaction mixture was concentrated in vacuo, and resulting residue was purified by flash column chromatography (15% ethyl acetate in petroleum ether to 50% ethyl acetate in petroleum ether) to provide 5-(2,6-dichloropyrimidin-4-yl)-3-(trifluoromethyl)pyridin-2-amine (300 mg, 59.3% yield). LCMS (ESI): [MH]+=308.7.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266862B2
Source datasetuspto-grants-2016_02
ORD IDord-164ab84daca64bfd8381e823dc25c02b
Source noteuspto-grants-2016_02