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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554887Generated: October 26, 2026

(S)-ethyl 2-(3-(4-fluorobenzyl)-4-methyl-2-oxoimidazolidin-1-yl)-4-methylthiazole-5-carboxylate → 2-(3-(But-3-enyl)-2-oxoimidazolidin-1-yl)-4-methylthiazole-5-carboxylic acid

https://huagongshe.com/reaction/554887

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-ethyl 2-(3-(4-fluorobenzyl)-4-methyl-2-oxoimidazolidin-1-yl)-4-methylthiazole-5-carboxylateHCID 57919865—
ReactantEthyl 2-(3-(but-3-enyl)-2-oxoimidazolidin-1-yl)-4-methylthiazole-5-carboxylateHCID 57919868—
Product2-(3-(But-3-enyl)-2-oxoimidazolidin-1-yl)-4-methylthiazole-5-carboxylic acidHCID 57920008—

Reaction Steps

Following the procedure as described in Preparation 6, making variations as required to replace (S)-ethyl 2-(3-(4-fluorobenzyl)-4-methyl-2-oxoimidazolidin-1-yl)-4-methylthiazole-5-carboxylate with ethyl 2-(3-(but-3-enyl)-2-oxoimidazolidin-1-yl)-4-methylthiazole-5-carboxylate, the title compound was obtained as a colourless solid (85%): mp 205-207° C.; 1H NMR (300 MHz, DMSO-d6) δ 12.70 (s, 1H), 5.86-5.72 (m, 1H), 5.16-5.02 (m, 2H), 4.01-3.96 (m, 2H), 3.60-3.54 (m, 2H), 3.31 (t, J=7.1 Hz, 2H), 2.50 (s, 3H), 2.32-2.26 (m, 2H); MS (ES+) m/z 281.8 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08049016B2
Source datasetuspto-grants-2011_11
ORD IDord-c2960715702249a7a9bc9c5a2e798bd3
Source noteuspto-grants-2011_11