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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202470Generated: November 2, 2026

1-(4-Fluorophenyl)-1H-pyrazol-5-ylboronic acid → 6-[2-(4-Fluoro-phenyl)-2H-pyrazol-3-yl]-1-(4-trifluoromethyl-phenyl)-1H-benzoimidazole

https://huagongshe.com/reaction/2202470

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Fluorophenyl)-1H-pyrazol-5-ylboronic acidHCID 90095170—
Reactant6-bromo-1-(4-trifluoromethyl-phenyl)-1H-benzo[d]imidazoleHCID 90095218—
Product6-[2-(4-Fluoro-phenyl)-2H-pyrazol-3-yl]-1-(4-trifluoromethyl-phenyl)-1H-benzoimidazoleHCID 73673673—

Reaction Steps

The title compound, light brown solid (67 mg, 54%), MS (ISP) m/z=423.3 [(M+H)+], mp 204° C., was prepared in accordance with the general method of example 1 from 6-bromo-1-(4-trifluoromethyl-phenyl)-1H-benzo[d]imidazole (intermediate I) (100 mg, 293 μmol) and 1-(4-fluoro-phenyl)-1H-pyrazol-5-ylboronic acid (intermediate A) (72.5 mg, 352 μmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365550B2
Source datasetuspto-grants-2016_06
ORD IDord-50ddf159acd74ff7b14c10142128aee2
Source noteuspto-grants-2016_06