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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1882373Generated: November 1, 2026

Potassium Carbonate → Ethyl 2-(3-((2,2-difluorocyclopropyl)methyl)-2-oxoimidazolidin-1-yl)-4-methylthiazole-5-carboxylate

https://huagongshe.com/reaction/1882373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-(Bromomethyl)-1,1-difluorocyclopropaneHCID 2761402—
ReactantEthyl 4-methyl-2-(2-oxoimidazolidin-1-yl)thiazole-5-carboxylateHCID 57919776—
Solvent1,4-DioxaneHCID 31275—
ProductEthyl 2-(3-((2,2-difluorocyclopropyl)methyl)-2-oxoimidazolidin-1-yl)-4-methylthiazole-5-carboxylateHCID 5791998154%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of ethyl 4-methyl-2-(2-oxoimidazolidin-1-yl)thiazole-5-carboxylate (1.19 g, 4.68 mmol) in anhydrous dioxane (50.0 mL) was added potassium carbonate (1.29 g, 9.36 mmol) and bromomethyl-2,2-difluorocyclopropane (1.00 g, 5.85 mmol). The reaction mixture was heated at 80° C. for 16 h, filtered and the solid was washed with ethyl acetate (100 mL). The filtrate was concentrated in vacuo and the residue was recrystallized from ethyl acetate in hexane to afford the title compound as a yellow solid (0.87 g, 54%): mp 146-148° C.; 1H NMR (300 MHz, CDCl3) δ 4.18 (q, J=7.1 Hz, 2H), 3.99 (t, J=8.4 Hz, 2H), 3.65-3.44 (m, 3H), 3.20-3.12 (m, 1H), 2.48 (s, 3H), 2.02-1.88 (m, 1H), 1.68-1.55 (m, 1H), 1.38-1.28 (m, 1H), 1.23 (t, J=7.1 Hz, 3H); 13C NMR (75 MHz, CDCl3) δ 162.5, 160.1, 156.8, 155.2, 114.9 (t), 113.8, 60.8, 42.4, 42.1, 41.1 (d), 20.3 (t, 2JC-F=43 Hz), 17.5, 14.9 (t, 2JC-F=43 Hz), 14.6; MS (ES+) m/z 399.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318949B2
Source datasetuspto-grants-2012_11
ORD IDord-441d536e094a4269b4ff8c5e24c3c6f6
Source noteuspto-grants-2012_11