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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706782Generated: October 30, 2026

Cesium carbonate → HCID 89464042, compound

https://huagongshe.com/reaction/706782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant1,4-DioxaneHCID 31275—
Reactant3,5-Dichloropyrazine-2-carbonitrileHCID 52987744—
ReactantHCID 89463765HCID 89463765—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventWaterHCID 962—
ProductHCID 89464042HCID 89464042—

Reaction Conditions

Temperature100 °C

Reaction Steps

5-Chloro-2-fluoro-N-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-benzenesulfonamide (709 mg) was added to a reaction vessel containing a magnetic stirring bar together with 3,5-dichloro-pyrazine-2-carbonitrile (300 mg), 1,1′-bis(diphenylphosphino)ferrocene-palladium(II) dichloride (Pd(dppf)2Cl2) (100 mg) and cesium carbonate (1.69 g), followed by 6 ml dioxane and 1 ml water, and the mixture heated to 100° C. under stirring. After 3 h the reaction mixture was cooled to RT and quenched with a saturated aqueous sodium bicarbonate solution (40 ml) and extracted with EtOAc (3×80 ml). The combined aqueous phases were dried over sodium sulfate, filtered and evaporated to afford the crude product as a brown oil. Purification by flash chromatography on silica gel using a mixture of EtOAc and heptane as the eluent afforded 5-chloro-N-[4-(6-chloro-5-cyano-pyrazin-2-yl)-phenyl]-2-fluoro-benzenesulfonamide as a brown foam after evaporation of the solvents under reduced pressure. Yield: 160 mg (22%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174993B2
Source datasetuspto-grants-2015_11
ORD IDord-b4c2c2575bbb41e69b5b6cef0d394987
Source noteuspto-grants-2015_11