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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1882363Generated: October 27, 2026

Ethyl bromoacetate → Ethyl 2-(3-(2-ethoxy-2-oxoethyl)-2-oxoimidazolidin-1-yl)-4-methylthiazole-5-carboxylate

https://huagongshe.com/reaction/1882363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 4-methyl-2-(2-oxoimidazolidin-1-yl)thiazole-5-carboxylateHCID 57919776—
SolventDimethylformamideHCID 6228—
ProductEthyl 2-(3-(2-ethoxy-2-oxoethyl)-2-oxoimidazolidin-1-yl)-4-methylthiazole-5-carboxylateHCID 5791975776%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of ethyl 4-methyl-2-(2-oxoimidazolidin-1-yl)thiazole-5-carboxylate (2.00 g, 7.83 mmol), ethyl bromoacetate (1.30 mL, 11.75 mmol) and potassium carbonate (1.62 g, 11.75 mmol) in N,N-dimethylformamide (20 mL) was stirred at 80° C. for 2 h. The reaction mixture was allowed to cool to ambient temperature, and then partitioned between ethyl acetate (75 mL) and water (50 mL). The aqueous layer was extracted with ethyl acetate (75 mL), and the combined organic layer was dried over sodium sulfate, filtered and concentrated in vacuo. The residue was triturated with ethyl acetate in hexanes to afford the title compound as a colorless solid (2.03 g, 76%): 1H NMR (300 MHz, CDCl3) δ 4.33-4.13 (m, 6H), 4.09 (s, 2H), 3.76-3.69 (m, 2H), 2.62 (s, 3H), 1.37-1.26 (m, 6H); MS (ES+) m/z 342.3 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318949B2
Source datasetuspto-grants-2012_11
ORD IDord-80126a2bd4d84bcc8d0af593662efb8e
Source noteuspto-grants-2012_11