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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715754Generated: October 30, 2026

4-(Aminomethyl)benzonitrile → 2-(4-cyanobenzylamino)-N-(imidazo[1,2-a]pyridin-6-yl)thiazole-5-carboxamide

https://huagongshe.com/reaction/715754

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Aminomethyl)benzonitrileHCID 82608—
Reactant2-bromo-N-(imidazo[1,2-a]pyridin-6-yl)thiazole-5-carboxamideHCID 86701929—
SolventAcetonitrileHCID 6342—
Product2-(4-cyanobenzylamino)-N-(imidazo[1,2-a]pyridin-6-yl)thiazole-5-carboxamideHCID 86701928—

Reaction Conditions

Temperature180 °C

Reaction Steps

To a solution of 2-bromo-N-(imidazo[1,2-a]pyridin-6-yl)thiazole-5-carboxamide (165 mg, 0.511 mmol) in acetonitrile (2553 μl) was added 4-cyanobenzylamine (67.5 mg, 0.511 mmol). The mixture was heated in a microwave (Biotage Initiator) at 180° C. for 30 minutes. The heating was repeated again after another equivalent of 4-cyanobenzylamine was added. The reaction mixture was purified by normal phase chromatography to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187472B2
Source datasetuspto-grants-2015_11
ORD IDord-a659ded7c8e843c392355d07d0c7e6bd
Source noteuspto-grants-2015_11