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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1024941Generated: October 30, 2026

Cesium carbonate → HCID 53628372, compound

https://huagongshe.com/reaction/1024941

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
Reactant1-AzetidinesulfonamideHCID 45080566—
ReactantHCID 86619884HCID 86619884—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 53628372HCID 53628372—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of azetidine-1-sulfonamide (prepared according to patent WO 2004/011443, 0.131 g), tris(dibenzylideneacetone)-dipalladium (0) (22 mg), 2-dicyclohexylphosphino-2′,4′,6′-tri-Isopropyl-1,1′-biphenyl (XPHOS) (11 mg), cesium carbonate (0.117 g) and 4-chloro-2-[(2,3-difluorobenzyl)thio]-6-((15)-1-[(2R)-1,4-dioxaspiro[4.5]dec-2-yl]ethoxy)pyrimidine (the product of step i) (0.100 g) in anhydrous dioxane (5 ml) was heated at reflux in a microwave at 100° C., 300 W, open vessel with cooling for 15 min. Saturated aqueous ammonium chloride was added and the resulting mixture extracted with EtOAc. The combined organic extracts were washed with saturated aqueous sodium chloride, dried with sodium sulfate, filtered and evaporated. The residue was purified by column chromatography on silica using a 1:19 to 3:7 mixture of EtOAc and iso-hexane as eluent and then, by reverse phase HPLC (gradient 25-95% acetonitrile in 0.1% ammonium acetate) to give the subtitle compound as a colourless gum. Yield: 43 mg

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722883B2
Source datasetuspto-grants-2014_05
ORD IDord-5c4db7339ec74a5c920733c0de8a05fd
Source noteuspto-grants-2014_05