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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 43561Generated: October 29, 2026

Thionyl Chloride → 4-Chloro-5-ethyl-1H-imidazole-2-carbonyl chloride

https://huagongshe.com/reaction/43561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant4-chloro-5-ethyl-1H-imidazole-2-carboxylic acidHCID 67548929—
Product4-Chloro-5-ethyl-1H-imidazole-2-carbonyl chlorideHCID 86648555—

Reaction Conditions

Temperature85 °C

Reaction Steps

Thionyl chloride (4 mL) was added to 4-chloro-5-ethyl-1H-imidazole-2-carboxylic acid (described in Example 1c, 200 mg, 0.8 mmol), and the mixture was stirred at 85° C. for 40 minutes. Following concentration under reduced pressure, the residue was azeotropically distilled with toluene twice to obtain crude 4-chloro-5-ethyl-1H-imidazole-2-carboxylic acid chloride. 5 mL pyridine was added and then ethyl 2-(4-aminophenyl)-1,3-thiazole-5-carboxylate obtained in Example (91b) was added. The mixture was stirred at room temperature for one hour. The reaction solution was diluted with ethyl acetate. The precipitated solid was collected by filtration and washed with ethyl acetate, to obtain 214 mg of the title compound as a white solid (73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536197B2
Source datasetuspto-grants-2013_09
ORD IDord-7363586aa9954a2bae59faa273ee7a24
Source noteuspto-grants-2013_09