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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1698552Generated: October 29, 2026

Sodium Bicarbonate → N-(4-Bromo-2-methoxy-6-methylphenyl)-7-(2,5-dimethyl-1H-pyrrol-1-yl)-1-methyl-1H-benzimidazol-2-amine

https://huagongshe.com/reaction/1698552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant4-Bromo-2-methoxy-6-methylanilineHCID 10680218—
Reactant2-Chloro-7-(2,5-dimethyl-1H-pyrrol-1-yl)-1-methyl-1H-benzimidazoleHCID 67273023—
ProductN-(4-Bromo-2-methoxy-6-methylphenyl)-7-(2,5-dimethyl-1H-pyrrol-1-yl)-1-methyl-1H-benzimidazol-2-amineHCID 5801241835%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 90 mg (0.347 mmol) of 2-chloro-7-(2,5-dimethyl-1H-pyrrol-1-yl)-1-methyl-1H-benzimidazole and 225 mg (1.04 mmol) of 4-bromo-2-methoxy-6-methylaniline was stirred at 110° C. for 15 hours. After cooling, the reaction mixture was neutralized by saturated aqueous sodium hydrogen carbonate and extracted with ethyl acetate (X2). The combined organic layer was washed with brine (X1), dried over sodium sulfate and concentrated in vacuo. The residue was purified by silica gel column chromatography eluting with a 60-90% ethylacetate/n-hexane gradient mixture. The desired fractions were collected and evaporated in vacuo, the residual solids were washed with diethyl ether to give 53.4 mg (35%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163935B2
Source datasetuspto-grants-2012_04
ORD IDord-cc32ebf868ba429a95bef9c51efb9729
Source noteuspto-grants-2012_04