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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2235562Generated: October 30, 2026

4-Bromo-2-methoxy-6-methylaniline → N-(4-Bromo-2-methoxy-6-methylphenyl)-7-(2-ethyl-1-piperidinyl)-1-methyl-1H-benzimidazol-2-amine

https://huagongshe.com/reaction/2235562

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-2-methoxy-6-methylanilineHCID 10680218—
Reactant2-Chloro-7-(2-ethyl-1-piperidinyl)-1-methyl-1H-benzimidazoleHCID 68581341—
SolventEthyl AcetateHCID 8857—
ProductN-(4-Bromo-2-methoxy-6-methylphenyl)-7-(2-ethyl-1-piperidinyl)-1-methyl-1H-benzimidazol-2-amineHCID 5889645230%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 2-chloro-7-(2-ethyl-1-piperidinyl)-1-methyl-1H-benzimidazole (100 mg, 0.36 mmol) and 4-bromo-2-methoxy-6-methylaniline (390 mg, 1.8 mmol) was heated at 110° C. for 12 h. The mixture was dissolved in ethyl acetate and washed with saturated sodium bicarbonate in water, dried over magnesium sulfate and concentrated under vacuum. The residue was purified by column chromatography eluting with a 15% acetone/hexanes mixture to afford 49.3 mg (30%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07714009B2
Source datasetuspto-grants-2010_05
ORD IDord-83f0d8b955794d2b902f749bd4fd511e
Source noteuspto-grants-2010_05