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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1517441Generated: November 2, 2026

Phenol → 6-(4-Fluorophenyl)-4-phenoxypyrido[3,2-d]pyrimidine

https://huagongshe.com/reaction/1517441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantSodium hydrideHCID 24758—
Reactant4-Chloro-6-(4-fluorophenyl)pyrido[3,2-d]pyrimidineHCID 57906756—
Solvent1,4-DioxaneHCID 31275—
Product6-(4-Fluorophenyl)-4-phenoxypyrido[3,2-d]pyrimidineHCID 5769834795%

Reaction Steps

To a solution of phenol (94 mg, 1 mmol) in dioxane (5 ml) was added sodium hydride (40 mg of a 60% dispersion in mineral oil, 1.0 mmol). The mixture was stirred at room temperature for 10 minutes. Then, 4-chloro-6-(4-fluorophenyl)-pyrido[3,2-d]pyrimidine (52 mg, 0.2 mmol) was added to this solution. The resulting mixture was stirred at room temperature for another 30 minutes. After concentration under reduced pressure, the residue was purified by silica gel flash chromatography, the mobile phase being a mixture of methanol and dichloromethane, in a volume ratio of 1:60, yielding the title compound (60 mg, yield 95%) as a white solid which was characterised by its mass spectrum as follows: MS (m/z): 318 ([M+H]+, 100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08232278B2
Source datasetuspto-grants-2012_07
ORD IDord-96bc3e0738444996a257257cf4e6ab72
Source noteuspto-grants-2012_07