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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284807Generated: October 31, 2026

Cesium carbonate → HCID 90052195, compound

https://huagongshe.com/reaction/2284807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant4-AminobenzonitrileHCID 13396—
Reactant1,4-DioxaneHCID 31275—
ReactantHCID 90051680HCID 90051680—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 90052195HCID 9005219515.7%

Reaction Conditions

Temperature100 °C

Reaction Steps

To tert-butyl (2-chloro-5-(5-hydroxy-1-pentyn-1-yl)pyridin-4-yl)(propyl)carbamate (S10, 88 mg), 4-aminobenzonitrile (59 mg), tris(dibenzylideneacetone)dipalladium(0) (22 mg), 4,5′-bis(diphenylphosphino)-9,9′-dimethylxanthene (29 mg) and cesium carbonate (203 mg), 1,4-dioxane (2.5 mL) was added at room temperature, and the mixture was stirred at 100° C. for 10 hours. The reaction mixture was cooled to room temperature, and then ethyl acetate and water were added to the reaction mixture. The insoluble matter was removed by filtration through Cerite. The organic layer was separated, washed with saturated aqueous sodium chloride, and then dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel chromatography (eluent, 100 to 30% hexane in ethyl acetate) to obtain tert-butyl (2-((4-cyanophenyl)amino)-5-(5-hydroxy-1-pentyn-1-yl)pyridin-4-yl)(propyl)carbamate (S11, 17 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145415B2
Source datasetuspto-grants-2015_09
ORD IDord-e73428a384f440b1b5fcd399093df536
Source noteuspto-grants-2015_09