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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710695Generated: November 3, 2026

Formamidine acetate → 6-(2-Furyl)-5-pyrimidin-4-ylpyrazin-2-amine

https://huagongshe.com/reaction/1710695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormamidine acetateHCID 160693—
Reactant1-[5-Amino-3-(2-furyl)pyrazin-2-yl]ethanoneHCID 59457632—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
SolventDimethylformamide dimethyl acetalHCID 78373—
Product6-(2-Furyl)-5-pyrimidin-4-ylpyrazin-2-amineHCID 1607166030%

Reaction Conditions

Temperature115 °C

Reaction Steps

A solution of 1-[5-amino-3-(2-furyl)pyrazin-2-yl]ethanone (Preparation 4, 388 mg, 1.91 mmol) in N,N-dimethylformamide dimethyl acetal (1.3 mL) was heated to 100° C. After 9 h, the mixture was concentrated under reduced pressure to yield brown oil. Formamidine acetate (795 mg, 7.64 mmol) was added to this oily residue previously dissolved in ethanol (6.4 mL) and toluene (0.96 mL). Molecular sieves (4 Å) were added to the solution and the whole reaction mixture was heated to 115° C. in a sealed tube and stirred for 20 h. The crude reaction was filtered and concentrated to dryness. The residue was partitioned between ethyl acetate and water, the organic layer was washed with brine, dried (Na2SO4) and evaporated. The residue was purified by silica gel flash chromatography (100% ethyl acetate). Concentration in vacuo of the product-rich fractions provided the titled compound as a pale-yellow solid (137 mg, 30%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790728B2
Source datasetuspto-grants-2010_09
ORD IDord-cc24f7a7a0c34c5bb06864d75bded878
Source noteuspto-grants-2010_09