HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710706Generated: November 1, 2026
Acetyl chloride → N-[6-(2-Furyl)-5-pyrimidin-4-ylpyrazin-2-yl]acetamide
https://huagongshe.com/reaction/1710706
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6-(2-Furyl)-5-pyrimidin-4-ylpyrazin-2-amine | HCID 16071660 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-[6-(2-Furyl)-5-pyrimidin-4-ylpyrazin-2-yl]acetamide | HCID 16070219 | 7% |
Reaction Steps
Sodium hydride (42 mg, 1.05 mmol) was added to a stirred solution of 6-(2-furyl)-5-pyrimidin-4-ylpyrazin-2-amine (Example 8, 100 mg, 0.42 mmol) in DMF (4 mL) at 0° C. under nitrogen. The solution was allowed to stir for 30 min. at 0° C. Acetyl chloride (60.0 μL, 0.84 mmol) was then added and the reaction mixture was warmed up to room temperature and stirred for 3 days. The reaction was diluted with ethyl acetate and washed with water. The organic layer was washed with brine, dried (Na2SO4) and evaporated. The residue was purified by silica gel flash chromatography (50% ethyl acetate in hexanes to 75% ethyl acetate in hexanes). Concentration in vacuo of the product-rich fractions provided the titled compound as a pale-yellow solid (8 mg, 7%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07790728B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-895fa5cbd86d4adcac5ad8a59a4dda19 |
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| Source note | uspto-grants-2010_09 |
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