Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1698558Generated: October 31, 2026

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

https://huagongshe.com/reaction/1698558

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-2-methoxy-6-methylanilineHCID 10680218—
Reactant2,4-Dichloro-7-(1-ethylpropyl)-1-methyl-1H-benzimidazoleHCID 67273025—
CatalystN-methyl-2-pyrrolidoneHCID 13387—
SolventWater ethylacetateHCID 22728543—
ProductN-(4-Bromo-2-methoxy-6-methylphenyl)-4-chloro-7-(1-ethylpropyl)-1-methyl-1H-benzimidazol-2-amineHCID 1197753849.1%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of 2,4-dichloro-7-(1-ethylpropyl)-1-methyl-1H-benzimidazole (140 mg, 0.52 mmol), 4-bromo-2-methoxy-6-methylaniline (335 mg, 1.55 mmol) and 1-methyl-2-pyrrolidone (5 drops) was stirred at 130° C. for 2 days under nitrogen atmosphere. The mixture was dissolved in ethyl acetate/water, extracted with ethyl acetate and washed with brine. The organic layer was dried over magnesium sulfate, and concentrated to give a brown oil. The oil was subjected to chromatography on a silica gel (n-hexane/ethyl acetate=10:1-1:1) and crystallized from iso-propanol to afford the title compound as colorless crystals (115 mg, 49%). mp. 218-220° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163935B2
Source datasetuspto-grants-2012_04
ORD IDord-3a233be1286149ef8ebda5b23d3989da
Source noteuspto-grants-2012_04