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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202473Generated: November 1, 2026

6-bromo-1-pyridin-4-yl-1H-benzoimidazole → 6-[2-(4-Chloro-phenyl)-2H-pyrazol-3-yl]-1-pyridin-4-yl-1H-benzoimidazole

https://huagongshe.com/reaction/2202473

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-bromo-1-pyridin-4-yl-1H-benzoimidazoleHCID 83450706—
Reactant1-(4-chloro-phenyl)-1H-pyrazol-5-ylboronic acidHCID 90095126—
Product6-[2-(4-Chloro-phenyl)-2H-pyrazol-3-yl]-1-pyridin-4-yl-1H-benzoimidazoleHCID 73671876—

Reaction Steps

The title compound, white solid (50 mg, 37%), MS (ISP) m/z=372.4 [(M+H)+], mp 203° C., was prepared in accordance with the general method of example 1 from 6-bromo-1-pyridin-4-yl-1H-benzoimidazole (intermediate L) (100 mg, 365 μmol) and 1-(4-chloro-phenyl)-1H-pyrazol-5-ylboronic acid (intermediate D) (97.4 mg, 438 μmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365550B2
Source datasetuspto-grants-2016_06
ORD IDord-ab0dd77f12d646bb835c1840838bca0d
Source noteuspto-grants-2016_06