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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654484Generated: October 31, 2026

Ammonia → 1H-Benzimidazol-6-amine, 5-chloro-1-(1-methylethyl)-2-(4-methyl-1-piperazinyl)-

https://huagongshe.com/reaction/1654484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHCID 15291316HCID 15291316—
CatalystZincHCID 23994—
SolventHydrochloric AcidHCID 313—
Product1H-Benzimidazol-6-amine, 5-chloro-1-(1-methylethyl)-2-(4-methyl-1-piperazinyl)-HCID 307329154.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

5-Chloro-1-isopropyl-2-(4-methyl-1-piperazinyl)-6-nitrobenzimidazole (1.2 g) was dissolved in 2.5N hydrochloric acid (20 ml) and thereto was added zinc powder (1.5 g) in portions and the mixture was stirred at 80° C. for 4 hours. The reaction mixture was made basic with an aqueous ammonia and extracted with chloroform. The chloroform layer was washed with water and dried over anhydrous magnesium sulfate and then the solvent was distilled off under reduced pressure. The residue was recrystallized from acetonitrile to give 6-amino-5-chloro-1-isopropyl-2-(4-methyl-1-piperazinyl)benzimidazole (0.6 g) as colorless crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05407936
Source datasetuspto-grants-1995_04
ORD IDord-9dfa155afd594b38a1759cd62cfa4652
Source noteuspto-grants-1995_04