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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428992Generated: October 30, 2026

2,3-Dichloroaniline → N-(2,3-dichlorophenyl)-2,5-dimethyl-1-phenyl-1H-imidazole-4-carboxamide

https://huagongshe.com/reaction/1428992

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-DichloroanilineHCID 11844—
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
Reactant2,5-dimethyl-1-phenyl-1H-imidazole-4-carboxylic acidHCID 54579222—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
ProductN-(2,3-dichlorophenyl)-2,5-dimethyl-1-phenyl-1H-imidazole-4-carboxamideHCID 5869575536%

Reaction Steps

Part A: To a magnetically stirred suspension of 2,5-dimethyl-1-phenyl-1H-imidazole-4-carboxylic acid (0.4 gram, 1.85 mmol) in CHCl3 (4 ml) was added oxalyl chloride (0.34 gram, 2.685 mmol) and the resulting mixture was reacted at 58° C. for 2 hours and subsequently concentrated in vacuo. The resulting residue was taken up in dichloromethane and diisopropylethylamine (0.28 gram, 2.148 mmol) was subsequently added. A solution of 2,3-dichloroaniline (0.35 gram, 2.146 mmol) in dichloromethane (5 ml) was slowly added to the resulting mixture and the resulting mixture was reacted for 2 hours at room temperature and subsequently concentrated in vacuo. The resulting residue was purified by flash chromatography (dichloromethane) to give N-(2,3-dichlorophenyl)-2,5-dimethyl-1-phenyl-1H-imidazole-4-carboxamide (0.24 gram, 36% yield). Melting point: 127-129° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937184B2
Source datasetuspto-grants-2015_01
ORD IDord-f0e7725abe794beb85a5373c25be010c
Source noteuspto-grants-2015_01