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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428115Generated: October 31, 2026

Cesium carbonate → 3-(4-Aminophenyl)-5-{1-[(2S)-1,4-dioxan-2-ylmethyl]-1H-pyrazol-4-yl}pyridin-2-amine

https://huagongshe.com/reaction/1428115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 2774010—
Reactant3-(4-Aminophenyl)-5-bromopyridin-2-amineHCID 68288976—
Reactant(2R)-1,4-dioxan-2-ylmethyl methanesulfonateHCID 86609782—
CatalystTetrabutylammonium IodideHCID 67553—
CatalystHCID 178418807HCID 178418807—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
Product3-(4-Aminophenyl)-5-{1-[(2S)-1,4-dioxan-2-ylmethyl]-1H-pyrazol-4-yl}pyridin-2-amineHCID 8670006871%

Reaction Steps

4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (10.0 g) was added to a suspension of cesium carbonate (75.6 g) in 1,4-dioxane (200 ml), followed by stirring. (2R)-1,4-Dioxan-2-ylmethyl methanesulfonate (12.1 g) and tetra-n-butylammonium iodide (0.95 g) were then added, and the mixture was stirred at 100° C. for six hours. After cooling the reaction solution to room temperature, 3-(4-aminophenyl)-5-bromopyridin-2-amine (10.9 g) and [1,1′-bis(diphenylphosphino)ferrocene]palladium(II) dichloride-dichloromethane adduct (2.1 g) were added, and the mixture was stirred at 100° C. for one hour. The reaction solution was returned to room temperature, ethyl acetate was added, and the insoluble matter was then removed by filtration. The resulting organic layer was sequentially washed with water and brine and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography [chloroform:methanol=99:1->19:1 (v/v)] to give 10.3 g of the title compound as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933103B2
Source datasetuspto-grants-2015_01
ORD IDord-69a61730e452476bb4d37b20566c34e4
Source noteuspto-grants-2015_01