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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600616Generated: October 29, 2026

2-Amino-5-(trifluoromethyl)pyridine → Phenyl[6-(trifluoromethyl)imidazo[1,2-a]pyridin-2-yl]methanone hydrobromide

https://huagongshe.com/reaction/600616

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-(trifluoromethyl)pyridineHCID 735862—
Reactant3-Bromo-1-phenylpropane-1,2-dioneHCID 12568911—
SolventDimethylformamideHCID 6228—
ProductPhenyl[6-(trifluoromethyl)imidazo[1,2-a]pyridin-2-yl]methanone hydrobromideHCID 6727354143.1%

Reaction Conditions

Temperature4 °C

Reaction Steps

To a solution of 0.324 g of 2-amino-5-trifluoromethylpyridine in 4 mL of DMF cooled to 4° C. is added dropwise a solution of 0.65 g of 3-bromo-1-phenylpropane-1,2-dione in 11 mL of DMF. The reaction mixture is stirred for 16 hours at 4° C. The precipitate is filtered off and washed with diethyl ether, and then dried. 0.32 g of phenyl[6-(trifluoromethyl)imidazo[1,2-a]pyridin-2-yl]methanone hydrobromide (1:1) is obtained in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902219B2
Source datasetuspto-grants-2011_03
ORD IDord-1fbcf3a0569b4952806c2985a0036409
Source noteuspto-grants-2011_03