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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554975Generated: November 3, 2026

Potassium Carbonate → 1-(5-Acetyl-4-methylthiazol-2-yl)-3-(2-cyclopropylethyl)imidazolidin-2-one

https://huagongshe.com/reaction/554975

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantToluene-4-sulfonic acid 2-cyclopropyl-ethyl esterHCID 13568392—
Reactant1-(5-Acetyl-4-methylthiazol-2-yl)imidazolidin-2-oneHCID 57919738—
CatalystTetrabutylammonium IodideHCID 67553—
Solvent1,4-DioxaneHCID 31275—
Product1-(5-Acetyl-4-methylthiazol-2-yl)-3-(2-cyclopropylethyl)imidazolidin-2-oneHCID 6666152137%

Reaction Steps

To a solution of 1-(5-acetyl-4-methylthiazol-2-yl)imidazolidin-2-one (4.50 g, 20.00 mmol), tetrabutylammonium iodide (0.10 g) and potassium carbonate (4.00 g, 28.92 mmol) in 1,4-dioxane (100 mL) was added 2-cyclopropylethyl-4-methylbenzenesulfonate (6.00 g, 24.96 mmol). The reaction mixture was heated to reflux for 37 h. The solvent was removed in vacuo. The residue was dissolved in water (50 mL) and extracted with ethyl acetate. The organic solution washed with water and brine and dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated in vacuo and the residue was purified by column chromatography to afford 1-(5-acetyl-4-methylthiazol-2-yl)-3-(2-cyclopropylethyl)imidazolidin-2-one in 37% yield (2.20 g): mp 82-83° C. (ethyl acetate/hexanes); 1H NMR (300 MHz, CDCl3) δ 4.12-4.06 (m, 2H), 3.63-3.57 (m, 2H), 3.40 (t, J=7.2 Hz, 2H), 2.60 (s, 3H), 2.44 (s, 3H), 1.51-1.44 (m, 2H), 0.71-0.62 (m, 1H), 0.49-0.43 (m, 2H), 0.09-0.04 (m, 2H); MS (ES+) m/z 294.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08049016B2
Source datasetuspto-grants-2011_11
ORD IDord-3eb151d0371241bdb6bdb320d0c1d826
Source noteuspto-grants-2011_11