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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 560596Generated: October 28, 2026

Ethyl 4-methyl-2-(2-oxo-3-phenylimidazolidin-1-yl)thiazole-5-carboxylate → 4-Methyl-2-(2-oxo-3-phenethylimidazolidin-1-yl)thiazole-5-carboxylic acid

https://huagongshe.com/reaction/560596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-methyl-2-(2-oxo-3-phenylimidazolidin-1-yl)thiazole-5-carboxylateHCID 58031446—
ReactantEthyl 4-methyl-2-(2-oxo-3-phenethylimidazolidin-1-yl)thiazole-5-carboxylateHCID 58031553—
Product4-Methyl-2-(2-oxo-3-phenethylimidazolidin-1-yl)thiazole-5-carboxylic acidHCID 5948120492%

Reaction Steps

Following the procedure as described in Example 5, making variations as required to replace ethyl 4-methyl-2-(2-oxo-3-phenylimidazolidin-1-yl)thiazole-5-carboxylate with ethyl 4-methyl-2-(2-oxo-3-phenethylimidazolidin-1-yl)thiazole-5-carboxylate, the title compound was obtained in 92% yield: 1H NMR (300 MHz, DMSO-d6) δ 7.29-7.14 (m, 5H), 3.92 (t, J=7.2 Hz, 2H), 3.53-3.41 (m, 4H), 2.79 (t, J=7.8 Hz, 2H), 2.46 (s, 3H); MS (ES+) m/z 332.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063084B2
Source datasetuspto-grants-2011_11
ORD IDord-3546576417ba41c38d2065ab1c2c1317
Source noteuspto-grants-2011_11