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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2194753Generated: October 30, 2026

3-[3-(3-Ethyl-5-isopropyl-2,6-dioxo-1,2,3,6-tetrahydro-pyrimidine-4-carbonyl)-5-methyl-phenyl]-acrylonitrile → 3-[3-(3-Ethyl-5-isopropyl-2,6-dioxo-pyrimidine-4-carbonyl)-5-methyl-phenyl]propanenitrile

https://huagongshe.com/reaction/2194753

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-[3-(3-Ethyl-5-isopropyl-2,6-dioxo-1,2,3,6-tetrahydro-pyrimidine-4-carbonyl)-5-methyl-phenyl]-acrylonitrileHCID 67050519—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product3-[3-(3-Ethyl-5-isopropyl-2,6-dioxo-pyrimidine-4-carbonyl)-5-methyl-phenyl]propanenitrileHCID 2521469994.3%

Reaction Steps

3-[3-(3-Ethyl-5-isopropyl-2,6-dioxo-1,2,3,6-tetrahydro-pyrimidine-4-carbonyl)-5-methyl-phenyl]-acrylonitrile (Compound 73) (190 mg, 0.54 mmol) was stirred with 10% palladium on carbon (20 mg) in anhydrous ethanol (10 mL) at room temperature under an atmosphere of hydrogen. After 17 hr., the reaction mixture was filtered through a celite pad and the pad was washed with ethanol and chloroform. The combined filtrate was evaporated in vacuo and the residue was purified by silica gel column chromatography (eluent, ethyl acetate:hexane (1:2)) to afford 180 mg (94%) of 3-[3-(3-ethyl-5-isopropyl-2,6-dioxo-1,2,3,6-tetrahydro-pyrimidine-4-carbonyl)-5-methyl-phenyl]-propionitrile (75) as a white foam. Recrystallization from chloroform-ether resulted in a white solid. m.p. 173-174° C.; 1H-NMR (300 MHz, CDCl3) δ 1.13-1.18 (6H, m), 1.23 (3H, d, J=6.9 Hz), 2.31 (1H, m), 2.47 (3H, s), 2.70 (2H, t, J=6.9 Hz), 3.04 (2H, t, J=6.9 Hz), 3.25 (1H, m), 3.89 (1H, m), 7.45 (1H, s), 7.66 (2H, s), 9.17 (1H, s); m/z (EI) 353 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08334295B2
Source datasetuspto-grants-2012_12
ORD IDord-2aef2f63d61447c982680d3a1d5a7baf
Source noteuspto-grants-2012_12