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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957092Generated: November 2, 2026

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

https://huagongshe.com/reaction/1957092

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): see Table 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05783521
Source datasetuspto-grants-1998_07
ORD IDord-b2fcf38660c241979648aae25f45e55c
Source noteuspto-grants-1998_07