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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629270Generated: October 29, 2026

4-Cyanophenylboronic acid → 4-(6-Bromoimidazo[1,2-a]pyridin-3-yl)benzonitrile

https://huagongshe.com/reaction/629270

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Cyanophenylboronic acidHCID 2734326—
Reactant6-Bromo-3-iodoimidazo(1,2-a)pyridineHCID 22031632—
Product4-(6-Bromoimidazo[1,2-a]pyridin-3-yl)benzonitrileHCID 89827150—

Reaction Steps

The title compound, light brown solid (0.47 g, 73%), MS (ISP) m/z=298.4 [(M+H)+], mp 176° 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-cyano-phenylboronic acid (0.36 g, 2.38 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315502B2
Source datasetuspto-grants-2016_04
ORD IDord-02e8038fa04c4acf956542deb2917f28
Source noteuspto-grants-2016_04