HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577124Generated: October 28, 2026
Potassium Carbonate → HCID 178462824, compound
https://huagongshe.com/reaction/577124
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Phosphorus tribromide | HCID 24614 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | (1-Ethyl-1H-imidazol-5-yl)methanol | HCID 22988641 | — |
| Reactant | HCID 178429541 | HCID 178429541 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178462824 | HCID 178462824 | 3.5% |
Reaction Steps
To the solution of (1-ethyl-1H-imidazol-5-yl)methanol (1.26 g, 10 mmol) in dioxane (50 mL) in a 250 mL round bottom flask, was added NCS (1.38 g, 10 mmol). The resulting mixture was stirred at room temperature overnight. Dioxane was removed under vacuum, and the crude solid was dissolved in chloroform (40 mL), followed by addition of PBr3 (1.9 mL, 20 mmol). The resulting mixture was stirred at room temperature overnight. The solvent was then evaporated. The crude 5-(bromomethyl)-4-chloro-1-ethyl-1H-imidazole was dissolved in DMF (20 mL). Potassium carbonate (3 g) and 6-methyl-2-sulfanylpyrimidin-4-ol (1.4 g, 10 mmol) were added. The mixture was stirred at room temperature for 2 hours. DMF was removed under vacuum, and the residue was purified by column chromatography to provide 2-{[(4-chloro-1-ethyl-1H-imidazol-5-yl)methyl]sulfanyl}-6-methylpyrimidin-4-ol (100 mg, 3% overall yield); 1H NMR (400 MHz, CD3OD): δ 1.41 (t, 3H), 2.29 (s, 3H), 4.12 (q, 1H), 4.60 (s, 2H), 4.59 (m, 1H), 6.01 (br, 1H), 7.66 (s, 1H); M+ 285.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040538B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-88604c3d5fae430599fd4ea170dda59a |
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| Source note | uspto-grants-2015_05 |
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