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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1779320Generated: October 30, 2026

Benzyl Alcohol → Benzyl 2-(4,6-dimethoxypyrimidin-2-yloxy)-6-(6-methoxypyridin-2-yl)benzoate

https://huagongshe.com/reaction/1779320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantPhosphoric AcidHCID 1004—
ReactantSodium hydrideHCID 24758—
Reactant4,6-Dimethoxy-2-(methylsulfonyl)pyrimidineHCID 838363—
Reactant2,2-Dimethyl-5-(6-methoxypyridin-2-yl)-4H-(1,3)benzodioxin-4-oneHCID 15279416—
SolventDimethylformamideHCID 6228—
ProductBenzyl 2-(4,6-dimethoxypyrimidin-2-yloxy)-6-(6-methoxypyridin-2-yl)benzoateHCID 15279417—

Reaction Steps

1.36 g of benzyl alcohol dissolved in 50 ml of dimethylformamide are treated with 380 mg of sodium hydride (80% strength in liquid paraffin) and the mixture is subsequently stirred at room temperature for about 1 h. 3.0 g of 2,2-dimethyl-5-(6-methoxypyridin-2-yl)-4H-(1,3)benzodioxin-4-one are added, the mixture is stirred at room temperature for 3 h and 2.65 g of 4,6-dimethoxy-2-methylsulfonylpyrimidine are finally added. The mixture is stirred at room temperature for 2 h, at 80° C. for 1.5 h and at 115° C. for 3 h, poured into ice-water containing phosphoric acid and extracted with ethyl acetate, and the organic phase is washed with water, dried over sodium sulfate and concentrated under reduced pressure. The crude product is purified by chromatography on silica gel 60 using cyclohexane/toluene/ethyl acetate. 1H-NMR (CDCl3): δ=3.80(s); 3.89(s); 5.02(s); 5.72(s); 6.67(d=; 6.7-7.7(m)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05627136
Source datasetuspto-grants-1997_05
ORD IDord-ce1161b634e94eaba1f67255d450caf5
Source noteuspto-grants-1997_05