Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1414729Generated: November 2, 2026

Water → HCID 21397137, compound

https://huagongshe.com/reaction/1414729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCyanogen BromideHCID 10476—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 14319499HCID 14319499—
SolventEthanolHCID 702—
ProductHCID 21397137HCID 2139713759%

Reaction Steps

To a solution of 2-[3-(4-methyl-1-piperazinyl)propylamino]-5-chloroaniline (70 g., 0.248 mole) in 350 ml. of water and 150 ml. ethanol was added, with stirring, 59.0 g. (0.557 mole) of cyanogen bromide in portions over 1 hour. The temperature was maintained at 40°-50° C. After the addition was completed the mixture was allowed to cool to room temperature and stirred overnight. After pouring into 1500 ml. ice water and making strongly alkaline with 20% NaOH, the precipitated solid was collected on a Buchner funnel, washed with water and dried in the vacuum oven to obtain 45.0 g. (59% yield) of crude 1-[3-(4-methyl-1-piperazinyl)propyl]-2-amino-5-chlorobenzimidazole, m.p. 223°-227° C. A portion was recrystallized from acetone as colorless needles, m.p. 228°-229.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04002623
Source datasetuspto-grants-1977_01
ORD IDord-bed5fe18644f403dacbd90e40dc64c49
Source noteuspto-grants-1977_01