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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 625953Generated: October 25, 2026

Potassium Fluoride → 3-(benzyloxy)-1-methyl-5-(4-phenylpyrimidin-2-yl)pyridin-2(1H)-one

https://huagongshe.com/reaction/625953

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium FluorideHCID 522689—
Reactant2-Chloro-4-phenylpyrimidineHCID 605356—
Reactant[5-(Benzyloxy)-1-methyl-6-oxo-1,6-dihydropyridin-3-yl]boronic acidHCID 67404944—
CatalystHCID 178418851HCID 178418851—
Solvent1,4-DioxaneHCID 31275—
Product3-(benzyloxy)-1-methyl-5-(4-phenylpyrimidin-2-yl)pyridin-2(1H)-oneHCID 6741944949%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of [5-(benzyloxy)-1-methyl-6-oxo-1,6-dihydropyridin-3-yl]boronic acid (30 mg, 0.116 mmol), 2-chloro-4-phenylpyrimidine (23.2 mg, 0.122 mmol), bis(tri-t-butylphosphine)palladium(0) (5.9 mg, 0.012 mmol) and potassium fluoride (24 mg, 0.405 mmol) in dioxane (1.5 mL) was stirred at 60° C. for 22 h, cooled to room temperature and filtered through a plug of silica gel (washed with EtOAc). Combined filtrate and washings were concentrated. Purification by preparative HPLC (5-55% CH3CN/H2O over 20 min, 0.05% added TFA) afforded 21 mg 3-(benzyloxy)-1-methyl-5-(4-phenylpyrimidin-2-yl)pyridin-2(1H)-one (49%) as a yellow solid. LC/MS (M+H)+ 370.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309199B2
Source datasetuspto-grants-2016_04
ORD IDord-3aae46562f2d492eb39237faeaf24c99
Source noteuspto-grants-2016_04