Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1790696Generated: October 25, 2026

Methyl iodide → (4-Bromophenyl)(5-nitrobenzimidazol-2-yl)amine

https://huagongshe.com/reaction/1790696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant4-Bromophenyl isothiocyanateHCID 16133—
Reactant4-Nitro-1,2-phenylenediamineHCID 5111791—
SolventMethanolHCID 887—
Product(4-Bromophenyl)(5-nitrobenzimidazol-2-yl)amineHCID 22041081—

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of the 4-nitrobenzene-1,2-diamine in methanol was treated with 4-bromo phenyl isothiocyanate (1 eq) and stirred at 60° C. for 2 hours. The reaction mixture was cooled down to room temperature and iodomethane (1 eq) was added and stirred overnight at 60° C. The reaction was concentrated and purified on silica gel to yield (4-bromophenyl)(5-nitrobenzimidazol-2-yl)amine. The product was taken in methanol and hydrogenated with catalytic amount of 10% Pd/C to give ((5-aminobenzimidazol-2-yl)(4-bromophenylamine). MS: MH+=302.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071216B2
Source datasetuspto-grants-2006_07
ORD IDord-b2672337f49f4fea831bf1a6c0ab6f63
Source noteuspto-grants-2006_07