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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51993Generated: October 25, 2026

Water → 5-(4,6-Dimethoxypyrimidin-2-yl)oxy-4-formyl-3-methylbenzothiophene

https://huagongshe.com/reaction/51993

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant4,6-Dimethoxy-2-(methylsulfonyl)pyrimidineHCID 838363—
Reactant4-Formyl-5-hydroxy-3-methylbenzothiopheneHCID 19077256—
SolventDimethylformamideHCID 6228—
Product5-(4,6-Dimethoxypyrimidin-2-yl)oxy-4-formyl-3-methylbenzothiopheneHCID 1907728286%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture comprising 2.1 g of 4-formyl-5-hydroxy-3-methylbenzothiophene, 2.4 g of 4,6-dimethoxy-2-methylsulfonylpyrimidine and 1.8 g of potassium carbonate in 30 ml of N,N-dimethylformamide, was heated and stirred at 70° C. for 3 hours. The mixture was returned to room temperature, then poured into water and extracted with ethyl acetate. The organic layer was washed with water and then dried over anhydrous sodium sulfate. Then, it was concentrated under reduced pressure, and the oily substance thereby obtained was purified by silica gel column chromatography (n-hexane/ethyl acetate=10/1) to obtain 3.1 g (yield: 86%) of the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616537
Source datasetuspto-grants-1997_04
ORD IDord-b85621a70dcc4cf1a64757f4dd2df935
Source noteuspto-grants-1997_04