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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57372Generated: October 29, 2026

Sodium hydride → 3-(2-Chloropyrimidin-4-yl)-4-(2-fluoropropan-2-yl)oxazolidin-2-one

https://huagongshe.com/reaction/57372

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2,4-DichloropyrimidineHCID 77531—
Reactant4-(2-Fluoropropan-2-yl)oxazolidin-2-oneHCID 90414475—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product3-(2-Chloropyrimidin-4-yl)-4-(2-fluoropropan-2-yl)oxazolidin-2-oneHCID 9041475057.4%

Reaction Steps

To the solution of 2,4-dichloropyrimidine (150 mg, 1.006 mmol) and 4-(2-fluoropropan-2-yl)oxazolidin-2-one (148 mg, 1.01 mmol) in DMF (4.5 mL), sodium hydride (60% wt. 89 mg, 2.21 mmol) was added to give a pale yellow mixture. The mixture was stirred at room temperature for 2 hr, diluted with EtOAc and stirred for additional 30 min. The separated organic layer was washed with saturated aqueous sodium bicarbonate solution, water and brine. The organic phase was dried over sodium sulfate, filtered off and concentrated under reduced pressure. The residue was purified by column chromatography [SiO2, 12 g, EtOAc/heptane=0/100 to 80/20] providing 3-(2-chloropyrimidin-4-yl)-4-(2-fluoropropan-2-yl)oxazolidin-2-one (150 mg) as a brown solid. MS m/z 260.1 (M+H)+; Rt-0.72 min. 1H NMR (400 Mhz, CDCl3) δ ppm 8.51 (d, J=5.9 Hz, 1H), 8.17 (d, J=5.9 Hz, 1H), 5.14 (dd, J=17.4, 8.0 Hz, 1H), 4.66 (d, J=9.4 Hz, 1H), 4.43-4.52 (m, 1H), 1.42-1.52 (m, 3H), 1.30-1.40 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434719B2
Source datasetuspto-grants-2016_09
ORD IDord-fbba7dda150a4475ae1577e37631de99
Source noteuspto-grants-2016_09