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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696717Generated: October 25, 2026

Ethanol → 2,3-Difluoro-N-[4-(2-trifluoromethyl-imidazo[1,2-a]pyridin-3-yl)-phenyl]-benzamide

https://huagongshe.com/reaction/1696717

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantStannous ChlorideHCID 24479—
ReactantDiisopropylethylamineHCID 81531—
Reactant3,4-Difluorobenzoyl chlorideHCID 2724519—
ReactantHCID 59296699HCID 59296699—
CatalystWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2,3-Difluoro-N-[4-(2-trifluoromethyl-imidazo[1,2-a]pyridin-3-yl)-phenyl]-benzamideHCID 1162586284%

Reaction Steps

To a solution of 690 mg (2.3 mmol) of 3-(4-Nitro-phenyl)-2-trifluoromethyl-imidazo[1,2-a]pyridine (n) in 30 mL of a 1:1 mixture of CH2Cl2 and ethanol (EtOH) was added 4.3 g (23 mmol) of SnCl2 and 4 drops of H2O. The reaction was allowed to stir overnight at which time it was concentrated in vacuo, and the resulting oil dissolved in 40 mL of EtOAc and washed 3 times with 50 mL of 2N NaOH. The organic layer was then dried over MgSO4 filtered and concentrated in vacuo. 73 mg (0.26 mmol) of the resulting solid was dissolved in 4 mL of CH2Cl2 to which 0.035 mL (0.27 mmol) of 3,4 difluorobenzoylchloride and 0.09 mL (0.52 mmol) diisopropyl ethyl amine (DIPEA) were added. The reaction was allowed to stir for 4 hrs at which time it was diluted with 20 mL CH2Cl2, quenched with 15 mL saturated aqueous NaHCO3 and washed with 15 mL brine. The organic layer was then dried over MgSO4 filtered and concentrated in vacuo. The crude oil was purified by silica gel chromatography 1:3 (EtOAc:Hexanes) to yield 91 mg (84%) of 2,3-Difluoro-N-[4-(2-trifluoromethyl-imidazo[1,2-a]pyridin-3-yl)-phenyl]-benzamide (Compound 70) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163777B2
Source datasetuspto-grants-2012_04
ORD IDord-b6bf3456c71d4a009491a00f1cfbdd8d
Source noteuspto-grants-2012_04