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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2361744Generated: October 31, 2026

2-Amino-4-bromopyridine-3-carbonitrile → 7-Bromo-3-(2,2,2-trifluoro-ethyl)-imidazo[1,2-a]pyridine-8-carbonitrile

https://huagongshe.com/reaction/2361744

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-4-bromopyridine-3-carbonitrileHCID 58081121—
Reactant2-Bromo-4,4,4-trifluorobutyraldehydeHCID 58081140—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product7-Bromo-3-(2,2,2-trifluoro-ethyl)-imidazo[1,2-a]pyridine-8-carbonitrileHCID 5808112848.8%

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of compounds D8 (2 g, 10.1 mmol) and D4 (2.898 g, 14.14 mmol) in EtOH (10 ml) was subjected to microwave heating at 150° C. for 40 min. After cooling to room temperature, the solvent was evaporated in vacuo. The residue thus obtained was diluted with EtOAc and washed with water. The organic layer was separated and washed with water, then with 1M HCl (aqueous solution), dried (MgSO4) and evaporated in vacuo. The crude product thus obtained was triturated with diethylether to yield compound D9 (1.5 g, 48.8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691813B2
Source datasetuspto-grants-2014_04
ORD IDord-4f1da4511e3c44189c88ec8c78263079
Source noteuspto-grants-2014_04