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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202462Generated: November 3, 2026

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

https://huagongshe.com/reaction/2202462

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-bromo-1-(4-fluoro-phenyl)-1H-benzo[d]imidazoleHCID 90095139—
Reactant1-(4-trifluoromethyl-phenyl)-1H-pyrazol-5-ylboronic acidHCID 90095240—
Product1-(4-Fluoro-phenyl)-6-[2-(4-trifluoromethyl-phenyl)-2H-pyrazol-3-yl]-1H-benzoimidazoleHCID 73673558—

Reaction Steps

The title compound, yellow solid (45 mg, 31%), MS (ISP) m/z=423.5 [(M+H)+], mp 167° C., was prepared in accordance with the general method of example 1 from 6-bromo-1-(4-fluoro-phenyl)-1H-benzo[d]imidazole (intermediate G) (100 mg, 344 μmol) and 1-(4-trifluoromethyl-phenyl)-1H-pyrazol-5-ylboronic acid (intermediate C) (96.7 mg, 378 μmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365550B2
Source datasetuspto-grants-2016_06
ORD IDord-be1ac6835a704bf491d6bcd787e0b2ab
Source noteuspto-grants-2016_06