Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625018Generated: October 26, 2026

Cesium carbonate → Ethyl (2R)-4-(5-fluoro-4-iodo-2-oxopyridin-1(2H)-yl)-2-methyl-2-(methylsulfonyl)butanoate

https://huagongshe.com/reaction/1625018

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant5-Fluoro-4-iodopyridin-2-olHCID 70664593—
Reactant(R)-ethyl 4-bromo-2-methyl-2-(methylsulfonyl)butanoateHCID 86670635—
SolventTetrahydrofuranHCID 8028—
ProductEthyl (2R)-4-(5-fluoro-4-iodo-2-oxopyridin-1(2H)-yl)-2-methyl-2-(methylsulfonyl)butanoateHCID 67249679—

Reaction Conditions

Temperature70 °C

Reaction Steps

Cesium carbonate (1.77 g, 5.44 mmol) was added to a suspension of 5-fluoro-4-iodopyridin-2(1H)-one (1.00 g, 4.2 mmol) and ethyl (2R)-4-bromo-2-methyl-2-(methylsulfonyl)butanoate (1.56 g, 5.44 mmol) in anhydrous THF (45 mL). The reaction was heated to 70° C. and stirred at this temperature overnight. The reaction was quenched with water (100 mL) and extracted with EtOAc (2×100 mL). The combined organics were washed with brine (100 mL), dried (MgSO4), filtered, and concentrated. The crude product was purified via flash chromatography using a Varian SF15-24 g column and an eluent of EtOAc in n-heptane (30-80%) to afford the title compound as a yellow residue (691 mg, 37%). MS (LCMS) m/z 446.0 (M+1). 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.36 (t, 3 H) 1.75 (s, 3 H) 2.37-2.57 (m, 2 H) 3.10 (s, 3 H) 3.83-4.02 (m, 1 H) 4.16-4.37 (m, 3 H) 7.15 (d, 1 H) 7.20 (d, J=3.32 Hz, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08779148B2
Source datasetuspto-grants-2014_07
ORD IDord-793813d657d14798920ec34b97d8b787
Source noteuspto-grants-2014_07