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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2244611Generated: November 2, 2026

Cyanogen Bromide → 1H-Benzimidazole-5-carbonitrile, 2-amino-

https://huagongshe.com/reaction/2244611

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantSodium HydroxideHCID 14798—
Reactant3,4-DiaminobenzonitrileHCID 737285—
SolventMethanolHCID 887—
Product1H-Benzimidazole-5-carbonitrile, 2-amino-HCID 11340065.5%

Reaction Conditions

Temperature20 °C

Reaction Steps

To a suspension of 3,4-diaminobenzonitrile (400 mg) in CH3OH (4 ml) was added BrCN (477 mg), followed by stirring at 20° C. for 14 hours. To the reaction mixture was added a 1M aqueous NaOH solution (0.117 ml), followed by concentration. To the residue was added chloroform:CH3OH=10:1 (10 ml), and the resulting insolubles were removed by filtration. The filtrate was concentrated, and the obtained residue was purified by silica gel column chromatography to obtain 2-amino-1H-benzimidazole-6-carbonitrile (311 mg) as pale orange color powders.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07678820B2
Source datasetuspto-grants-2010_03
ORD IDord-3cf0c23134104627926c4eb231bd4166
Source noteuspto-grants-2010_03