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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522656Generated: October 28, 2026

2-Fluorophenol → Tert-butyl 4-(5-(2-fluorophenoxyl)pyrimidin-2-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/522656

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-FluorophenolHCID 9707—
ReactantCesium carbonateHCID 10796—
Reactanttert-Butyl 4-(5-bromopyrimidin-2-yl)piperazine-1-carboxylateHCID 21914476—
CatalystCopperHCID 23978—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 4-(5-(2-fluorophenoxyl)pyrimidin-2-yl)piperazine-1-carboxylateHCID 1180221706.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of tert-butyl 4-(5-bromopyrimidin-2-yl)piperazine-1-carboxylate (684 mg, 2.0 mmol), 2-fluorophenol (1.1 g, 10.0 mmol), copper (650 mg, 10.0 mmol) and cesium carbonate (6.5 g, 20.0 mmol) in pyridine (15 mL) was heated at 120 0° C. in a sealed tube overnight. The reaction mixture was diluted with ethyl acetate (200 mL) and then filtered. The filtrate was concentrated, and the residue was purified by silica gel chromatography (petroleum ether:ethyl acetate 20:1) to give tert-butyl 4-(5-(2-fluorophenoxyl)pyrimidin-2-yl)piperazine-1-carboxylate (50 mg, 6%) as a yellow solid. MS (ES+) C19H23FN4O3 requires: 374, found: 397 [M+Na]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334263B2
Source datasetuspto-grants-2016_05
ORD IDord-f8c3de02037a49d7874e63e5ecee6d70
Source noteuspto-grants-2016_05