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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2299165Generated: October 31, 2026

Chloroform → 4-Bromo-7-methyl-5-aminobenzimidazole

https://huagongshe.com/reaction/2299165

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantDimethylformamideHCID 6228—
ReactantTetramethyltinHCID 11661—
Reactant4,7-Dibromo-5-aminobenzimidazoleHCID 18379891—
CatalystHCID 178418476HCID 178418476—
Product4-Bromo-7-methyl-5-aminobenzimidazoleHCID 1837983329%
Product4,7-dimethyl-3H-benzimidazol-5-amineHCID 18379861—

Reaction Conditions

Temperature140 °C

Reaction Steps

A solution of 4,7-dibromo-5-aminobenzimidazole (1.5 g, 5.1 mmol) in 10 ml of DMF was transferred into pressure bottle under Ar2. To the solution was added tetramethyltin (3.6 ml, 20 mmol). and bis(triphenylphosphine)palladium(II) chloride (200 mg). The resulting reaction mixture was stirred at 140° C. for 24 h and concentrated in vacuo, yielding a dark oil which was subjected to column chromatography (40% EtOAC/CHCl3) to yield 0.34 g (1.5 mmol, 29%) of the desired product as well as 0.75 g of 4,7-dimethyl-5-aminobenzimidazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06495583B1
Source datasetuspto-grants-2002_12
ORD IDord-89d589deb21346a5b9fef6bd37703ebe
Source noteuspto-grants-2002_12