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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828834Generated: October 31, 2026

4-Fluorophenol → HCID 20872664, compound

https://huagongshe.com/reaction/1828834

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorophenolHCID 9732—
ReactantCesium carbonateHCID 10796—
ReactantHCID 20872663HCID 20872663—
SolventDimethylformamideHCID 6228—
ProductHCID 20872664HCID 2087266453.4%

Reaction Steps

4-[(2-Chloro-5-fluoro-pyridine-3-carbonyl)-amino]-piperidine-1-carboxylic acid tert-butyl ester (4.0 g, 11.18 mmol) (see Preparation 27), 4-fluorophenol (1.378 g, 12.3 mmol) and caesium carbonate (7.29 g, 33.54 mmol) were stirred in N,N-dimethylformamide (40 ml) at 55° C. under an atmosphere of nitrogen for 18 hours. The reaction mixture was then partitioned between ethyl acetate (50 ml) and water (30 ml) and the organic layer separated. The organic layer was then washed with a saturated aqueous solution of sodium chloride (40 ml), dried over anhydrous magnesium sulphate and the solvent removed in vacuo. The residue was purified by flash column chromatography on silica gel eluting with dichloromethane. The product was finally triturated with diethylether (25 ml) giving 4-{[5-fluoro-2-(4-fluorophenoxy)-pyridine-3-carbonyl]-amino}-piperidine-1-carboxylic acid tert-butyl ester (2.59 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07060717B2
Source datasetuspto-grants-2006_06
ORD IDord-d6a6690fcdc94d70bc4a19915710b352
Source noteuspto-grants-2006_06