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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554900Generated: November 4, 2026

Potassium Carbonate → Ethyl 4-methyl-2-(2-oxoimidazolidin-1-yl)thiazole-5-carboxylate

https://huagongshe.com/reaction/554900

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloroethyl isocyanateHCID 16035—
ReactantEthyl 2-amino-4-methylthiazole-5-carboxylateHCID 343747—
CatalystTetrabutylammonium IodideHCID 67553—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 4-methyl-2-(2-oxoimidazolidin-1-yl)thiazole-5-carboxylateHCID 5791977671%

Reaction Steps

To a solution of ethyl 2-amino-4-methylthiazole-5-carboxylate (9.31 g, 49.99 mmol) in tetrahydrofuran (200 mL) was added 2-chloroethyl isocyanate (5.50 mL, 64.0 mmol) at ambient temperature. The resulting reaction mixture was heated to reflux for 7 hours, followed by the addition of potassium carbonate (8.30 g, 60.0 mmol) and tetra-n-butylammonium iodide (0.50 g, 1.35 mmol) and the resulting mixture was heated to reflux for 23 hours. The solvent was removed in vacuo, and the residue was washed with water (200 mL) and ethyl acetate (50 mL) to afford the title compound in 71% yield (9.10 g): mp 197-199° C.; 1H NMR (300 MHz, DMSO-d6) δ 7.83 (s, 1H), 4.20-3.93 (m, 4H), 3.49-3.43 (m, 2H), 2.46 (s, 3H), 1.20 (t, J=6.9 Hz, 3H); MS (ES+) m/z 256.3 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08049016B2
Source datasetuspto-grants-2011_11
ORD IDord-6373619be34d4a0c88e5c3fad67ad0e5
Source noteuspto-grants-2011_11