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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2186114Generated: October 31, 2026

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

https://huagongshe.com/reaction/2186114

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 18379833290%
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, 290%) 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 numberUS06403626B1
Source datasetuspto-grants-2002_06
ORD IDord-cb28f360f8744dd38a64e8533f81ceb4
Source noteuspto-grants-2002_06