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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4,6-Dimethoxy-2-(methylsulfonyl)pyrimidine | HCID 838363 | — |
| Reactant | 4-Formyl-5-hydroxy-3-methylbenzothiophene | HCID 19077256 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-(4,6-Dimethoxypyrimidin-2-yl)oxy-4-formyl-3-methylbenzothiophene | HCID 19077282 | 86% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05616537 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-b85621a70dcc4cf1a64757f4dd2df935 |
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| Source note | uspto-grants-1997_04 |
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