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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2081035Generated: October 31, 2026

2,4-Dichlorobenzylamine → N-[(2,4-dichlorophenyl)methyl]-3-ethyl-1-methyl-2-oxo-4-imidazolidinecarboxamide

https://huagongshe.com/reaction/2081035

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DichlorobenzylamineHCID 1485—
ReactantEthylmorpholineHCID 7525—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant3-Ethyl-1-methyl-2-oxo-4-imidazolidinecarboxylic acidHCID 67103633—
SolventDichloromethaneHCID 6344—
ProductN-[(2,4-dichlorophenyl)methyl]-3-ethyl-1-methyl-2-oxo-4-imidazolidinecarboxamideHCID 2509517353.4%

Reaction Steps

A mixture of 3-ethyl-1-methyl-2-oxo-4-imidazolidinecarboxylic acid (138 mg, 0.800 mmol), 1-hydroxybenzotriazole hydrate (147 mg, 0.960 mmol), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (184 mg, 0.960 mmol) and N-ethyl morpholine (0.409 ml, 3.20 mmol) in dichloromethane (9 ml) was stirred at room temperature for 10 minutes. A solution of [1-(2,4-dichlorophenyl)methyl]amine (141 mg, 0.8 mmol) in dichloromethane (1 ml) was added and the reaction mixture was stirred at room temperature for 18 hours. The reaction mixture was diluted with dichloromethane (10 ml) and the solution was washed with saturated sodium hydrogen carbonate solution (10 ml), water (10 ml), citric acid solution (10 ml) and brine (10 ml), dried and evaporated. The residue was purified by mass-directed automated HPLC. The residue was triturated with ether and the resulting solid was collected and dried to give N-[(2,4-dichlorophenyl)methyl]-3-ethyl-1-methyl-2-oxo-4-imidazolidinecarboxamide (141 mg, 53%). LC/MS [M+H]+=330, retention time=2.36 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932282B2
Source datasetuspto-grants-2011_04
ORD IDord-d6bb53d20af344028ecb74b6934ff447
Source noteuspto-grants-2011_04