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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750313Generated: October 31, 2026

Cesium carbonate → 5-Phenyl-3-(2,2,2-trifluoroethyl)furo[2,3-d]pyrimidin-4(3H)-one

https://huagongshe.com/reaction/1750313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant1,1,1-Trifluoro-2-iodoethaneHCID 67709—
Reactant5-phenylfuro[2,3-d]pyrimidin-4(3H)-oneHCID 59427830—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product5-Phenyl-3-(2,2,2-trifluoroethyl)furo[2,3-d]pyrimidin-4(3H)-oneHCID 11785715626.3%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 5-phenylfuro[2,3-d]pyrimidin-4(3H)-one (2 g, 9.42 mmol, prepared as described in WO2006/004658) in DMF (20 ml) was charged cesium carbonate (6.76 g, 20.7 mmol) and 1,1,1-trifluoro-2-iodoethane (1.86 ml, 18.9 mmol). The reaction was heated at 70° C. for 18 h under a nitrogen atmosphere. A further 1 eq. of 1,1,1-trifluoro-2-iodoethane was charged to the reaction mixture. The reaction was heated to 100° C. for 5 h before being cooled to RT, diluted with water and extracted twice with ethyl acetate. The organic extracts were washed with brine (3×50 ml), dried (Na2SO4), filtered and concentrated in vacuo. The resultant residue was purified by silica gel chromatography (SiO2, 0 to 50% EtOAc in cyclohexane) affording the title compound as a beige solid (730 mg, 26%). LCMS RT=1.27 min, M+H+=295.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156853B2
Source datasetuspto-grants-2015_10
ORD IDord-649a2766c3da49bdb2e8e1f64e58d77c
Source noteuspto-grants-2015_10