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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408477Generated: October 29, 2026

Cesium carbonate → tert-butyl (3S,5R)-1-(3-(2-(2,6-difluorophenyl)-quinazolin-8-ylamino)pyridin-4-yl)-5-methylpiperidin-3-ylcarbamate

https://huagongshe.com/reaction/408477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantBinap, (A+-)-HCID 634876—
ReactantHCID 58386794HCID 58386794—
Reactant2-(2,6-Difluorophenyl)quinazolin-8-yl trifluoromethanesulfonateHCID 86656442—
Catalystpalladium(II) acetateHCID 167845—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
Producttert-butyl (3S,5R)-1-(3-(2-(2,6-difluorophenyl)-quinazolin-8-ylamino)pyridin-4-yl)-5-methylpiperidin-3-ylcarbamateHCID 8665644379%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of the tert-butyl (3S,5R)-1-(3-aminopyridin-4-yl)-5-methylpiperidin-3-ylcarbamate (1.0 eq) in 1,4-dioxane (0.067M) was added 2-(2,6-difluorophenyl)quinazolin-8-yl trifluoromethanesulfonate (1.0 eq), palladium acetate (0.2 eq), BINAP (1.5 eq), and cesium carbonate (3.0 eq). The reaction mixture was stirred at 120° C. for 10 min in microwave. The residue was dissolved in ethyl acetate (120 mL), and washed with water, brine, then dried over MgSO4, filtered, and evaporated under reduced pressure to give crude product, which was purified by column (ethyl acetate:hexanes=1:1 with 10% methanol) to yield tert-butyl (3S,5R)-1-(3-(2-(2,6-difluorophenyl)-quinazolin-8-ylamino)pyridin-4-yl)-5-methylpiperidin-3-ylcarbamate (79%). LC/MS (m/z): 547.1 (MH+), Rt=0.87

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759338B2
Source datasetuspto-grants-2014_06
ORD IDord-2d09762c81874f7a8fbe5b5eaf01c4d4
Source noteuspto-grants-2014_06