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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1276871Generated: October 31, 2026

Acetic Anhydride → 6-Acetylamino-1-(2-chlorobenzyl)-2-n-propylbenzimidazole

https://huagongshe.com/reaction/1276871

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
Reactant1-(2-Chlorobenzyl)-2-propyl-1H-benzo[d]imidazol-6-amineHCID 12042348—
SolventDichloromethaneHCID 6344—
Product6-Acetylamino-1-(2-chlorobenzyl)-2-n-propylbenzimidazoleHCID 2262033483.6%

Reaction Steps

Acetic anhydride (62 mg) was added to a solution of 150 mg of 6-amino-1-(2-chlorobenzyl)-2-n-propylbenzimidazole and 61 mg of triethylamine in 3 ml of methylene chloride at room temperature, and the mixture was stirred for 1 hour. The reaction mixture was washed with water, and was then dried. The solvent was distilled off under reduced pressure. The residue was crystallized with ether to give 143 mg of 6-acetylamino-1-(2-chlorobenzyl)-2-n-propylbenzimidazole (89).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06166219
Source datasetuspto-grants-2000_12
ORD IDord-f72137fc1611474db50d74ccc2f1060a
Source noteuspto-grants-2000_12