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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202464Generated: October 31, 2026

6-bromo-1-(4-chloro-phenyl)-1H-benzo[d]imidazole → 1-(4-Chloro-phenyl)-6-[2-(4-trifluoromethyl-phenyl)-2H-pyrazol-3-yl]-1H-benzoimidazole

https://huagongshe.com/reaction/2202464

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-bromo-1-(4-chloro-phenyl)-1H-benzo[d]imidazoleHCID 90095072—
Reactant1-(4-trifluoromethyl-phenyl)-1H-pyrazol-5-ylboronic acidHCID 90095240—
Product1-(4-Chloro-phenyl)-6-[2-(4-trifluoromethyl-phenyl)-2H-pyrazol-3-yl]-1H-benzoimidazoleHCID 73673560—

Reaction Steps

The title compound, light brown solid (56 mg, 39%), MS (ISP) m/z=439.4 [(M+H)+], mp 198° C., was prepared in accordance with the general method of example 1 from 6-bromo-1-(4-chloro-phenyl)-1H-benzo[d]imidazole (intermediate H) (100 mg, 325 μmol) and 1-(4-trifluoromethyl-phenyl)-1H-pyrazol-5-ylboronic acid (intermediate C) (91.6 mg, 358 μmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365550B2
Source datasetuspto-grants-2016_06
ORD IDord-26795d3fc32542c695c39daf29ee2f0f
Source noteuspto-grants-2016_06