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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629263Generated: October 29, 2026

4-Chlorophenylboronic acid → 6-Bromo-3-(4-chlorophenyl)imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/629263

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorophenylboronic acidHCID 74299—
Reactant6-Bromo-3-iodoimidazo(1,2-a)pyridineHCID 22031632—
Product6-Bromo-3-(4-chlorophenyl)imidazo[1,2-a]pyridineHCID 89826716—

Reaction Steps

The title compound, light yellow solid (0.28 g, 42%), MS (ISP) m/z=307.3 [(M+H)+], mp 157° C., was prepared in accordance with the general method of intermediate E from commercially available 6-bromo-3-iodoimidazo[1,2-a]pyridine (0.7 g, 2.17 mmol) and commercially available 4-chloro-phenylboronic acid (0.34 g, 2.17 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315502B2
Source datasetuspto-grants-2016_04
ORD IDord-5d3491c555bf4797b0fbc54bcd67e821
Source noteuspto-grants-2016_04