HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1674368Generated: October 31, 2026
Dimethyl Sulfoxide → HCID 57461033, compound
https://huagongshe.com/reaction/1674368
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2,3-Dihydro-2,2-dimethyl-7-benzofuranol | HCID 15278 | — |
| Reactant | 4'-[(5-bromo-4-ethyl-6-oxo-2-propylpyrimidin-1(6H)-yl)methyl]biphenyl-2-carbonitrile | HCID 57460066 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 57461033 | HCID 57461033 | 39.2% |
Reaction Steps
A mixture of 4′-[(5-bromo-4-ethyl-6-oxo-2-propylpyrimidin-1(6H)-yl)methyl]biphenyl-2-carbonitrile (0.45 g), 2,2-dimethyl-2,3-dihydro-1-benzofuran-7-ol (0.25 g), 8 M potassium hydroxide solution (0.19 mL) and dimethyl sulfoxide (8 mL) was stirred at 150° C. for 12 hr. The reaction mixture was diluted with ethyl acetate, washed with water and then with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography to give the title compound as a colorless amorphous solid (0.21 g, 39%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07998968B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-a2166b3376d94b889b195aa7c733f906 |
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| Source note | uspto-grants-2011_08 |
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