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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356981Generated: October 30, 2026

4-Chlorobenzoyl chloride → 4-Chloro-N-[3-(1H-imidazol-1-yl)propyl]benzamide

https://huagongshe.com/reaction/356981

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzoyl chlorideHCID 8501—
Reactant1H-Imidazole-1-propanamineHCID 78736—
ReactantDiisopropylethylamineHCID 81531—
SolventDichloromethaneHCID 6344—
Product4-Chloro-N-[3-(1H-imidazol-1-yl)propyl]benzamideHCID 2842664—

Reaction Steps

To a solution of 1-(3-amino-propyl)imidazole (2.1 g, 16.8 mmol), diisopropyl-ethylamine (3.5 mL, 20.0 mmol) and 4-N,N-dimethyl-aminopyridine (200 mg, 1.7 mmol) in methylene chloride (15 mL) at 0° C. was added dropwise 4-chlorobenzoyl-chloride (2.1 mL, 16.8 mmol). The reaction was then allowed to warm to room temperature. After 5 hours, the reaction was diluted with methylene chloride, washed with 1N sodium hydroxide, brine, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo to provide a white solid. This material was washed with diethyl ether to provide N-(3-imidazol-1-yl-propyl)-4-chlorobenzamide. To a slurry of the above amide (1.58 g, 6.0 mmol) in tetrahydrofuran (30 mL) was slowly added lithium aluminum hydride (456 mg, 12.0 mmol) upon which the reaction became exothermic. The mixture was heated to 80° C., stirred for 1 hr, cooled to 0° C. and quenched by addition of water (0.5 mL), 15% sodium hydroxide (0.5 mL) and an additional 1.5 mL of water. The reaction was diluted with ethyl acetate, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo to provide compound 20.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05840736
Source datasetuspto-grants-1998_11
ORD IDord-c3dce65ba56b49ea87ed2ef7b85e228f
Source noteuspto-grants-1998_11