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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantSodium hydrideHCID 24758—
Reactant6-(2-Furyl)-5-pyrimidin-4-ylpyrazin-2-amineHCID 16071660—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductN-[6-(2-Furyl)-5-pyrimidin-4-ylpyrazin-2-yl]acetamideHCID 160702197%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790728B2
Source datasetuspto-grants-2010_09
ORD IDord-895fa5cbd86d4adcac5ad8a59a4dda19
Source noteuspto-grants-2010_09