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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554929Generated: November 3, 2026

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

https://huagongshe.com/reaction/554929

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantBromomethylcyclopropaneHCID 81503—
Reactant1-(5-Acetyl-4-methylthiazol-2-yl)imidazolidin-2-oneHCID 57919738—
CatalystTetrabutylammonium IodideHCID 67553—
SolventTetrahydrofuranHCID 8028—
Product1-(5-Acetyl-4-methylthiazol-2-yl)-3-(cyclopropylmethyl)imidazolidin-2-oneHCID 5791976333%

Reaction Steps

To a solution of 1-(5-acetyl-4-methylthiazol-2-yl)imidazolidin-2-one (2.25 g, 10.00 mmol), tetrabutylammonium iodide (0.10 g) and potassium carbonate (3.50 g, 25.27 mmol) in tetrahydrofuran (100 mL) was added cyclopropylmethyl bromide (2.0 mL, 20.88 mmol). The reaction mixture was heated to reflux for 50 hours. The solvent was removed in vacuo, and the residue was washed with water and hexanes to afford the title compound in 33% yield (0.94 g): mp 103-104° C. (ethyl acetate/hexanes); 1H NMR (300 MHz, CDCl3) δ 4.14-4.05 (m, 2H), 3.72-3.69 (m, 2H), 3.19 (d, J=6.0 Hz, 2H), 2.57 (s, 3H), 2.44 (s, 3H), 0.99-0.89 (m, 1H), 0.59-0.55 (m, 2H), 0.27-0.22 (m, 2H); MS (ES+) m/z 280.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08049016B2
Source datasetuspto-grants-2011_11
ORD IDord-e573ff120c1d49638b5db0234b518ae1
Source noteuspto-grants-2011_11