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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1955990Generated: November 1, 2026

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

https://huagongshe.com/reaction/1955990

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 1 h. 3.0 g of 2,2-dimethyl-5-(6-methoxypyridin-2-yl)-4H-(1,3)benzo-dioxin-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 extract is washed with water, dried over sodium sulfate and concentrated in vacuo. The crude product is purified by chromatography on silica gel 60 using cyclohexane/toluene/ethyl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05777118
Source datasetuspto-grants-1998_07
ORD IDord-0f467423724848ffac9455041c2e4d75
Source noteuspto-grants-1998_07