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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 410642Generated: November 2, 2026

Cesium carbonate → tert-Butyl 4-((2-chloropyrimidin-4-yl)oxy)piperidine-1-carboxylate

https://huagongshe.com/reaction/410642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant2,4-DichloropyrimidineHCID 77531—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Producttert-Butyl 4-((2-chloropyrimidin-4-yl)oxy)piperidine-1-carboxylateHCID 7162990681%

Reaction Conditions

Temperature80 °C

Reaction Steps

To tert-butyl 4-hydroxypiperidine-1-carboxylate (389 mg, 1.933 mmol) and 2,4-dichloropyrimidine (240 mg, 1.611 mmol) in DMF (6.4 mL) was added cesium carbonate (1050 mg, 3.22 mmol) and the mixture was heated at 80° C. for 1 h and then to 70° C. overnight. TLC indicated no remaining 2,4-dichloropyrimidine. The reaction was cooled to ambient temperature, diluted with water and extracted with ethyl acetate. The organic layer was washed with water (3×) and brine. The combined organic layer was dried (MgSO4), filtered and solvent was removed under reduced pressure. The residue was purified by column chromatography on silica gel to give tert-butyl 4-[(2-chloropyrimidin-4-yl)oxy]piperidine-1-carboxylate (410 mg, 1.3 mmol, 81%) as white solid. MS ESI: [M+H]+ m/z 314.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759366B2
Source datasetuspto-grants-2014_06
ORD IDord-1b208c4610ab45acbf8a1d3990a0681e
Source noteuspto-grants-2014_06