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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 560701Generated: October 26, 2026

1-(Bromomethyl)-4-(trifluoromethyl)benzene → Ethyl 4-methyl-2-(2-oxo-3-(pyridin-4-ylmethyl) imidazolidin-1-yl)thiazole-5-carboxylate

https://huagongshe.com/reaction/560701

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Bromomethyl)-4-(trifluoromethyl)benzeneHCID 123062—
Reactant4-(Bromomethyl)pyridineHCID 642799—
ReactantEthyl 4-methyl-2-(2-oxoimidazolidin-1-yl)thiazole-5-carboxylateHCID 57919776—
ProductEthyl 4-methyl-2-(2-oxo-3-(pyridin-4-ylmethyl) imidazolidin-1-yl)thiazole-5-carboxylateHCID 58031451—

Reaction Steps

Following the procedure as described in Example 13, making variations as required to replace 4-(trifluoromethyl)benzyl bromide with 4-(bromomethyl)pyridine to react with ethyl 4-methyl-2-(2-oxoimidazolidin-1-yl)thiazole-5-carboxylate, the title compound was obtained as a colorless solid in quantitative yield: MS (ES+) m/z 347.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063084B2
Source datasetuspto-grants-2011_11
ORD IDord-65805a547b264e7f996605881223a6b4
Source noteuspto-grants-2011_11