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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 38807Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/38807

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktStannous ChlorideHCID 24479—
EduktDiisopropylethylamineHCID 81531—
Edukt3,4-Difluorobenzoyl chlorideHCID 2724519—
EduktHCID 59296699HCID 59296699—
KatalysatorWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produkt2,3-Difluoro-N-[4-(2-trifluoromethyl-imidazo[1,2-a]pyridin-3-yl)-phenyl]-benzamideHCID 1162586284%

Reaktionsschritte

To a solution of 690 mg (2.3 mmol) of 3-(4-Nitro-phenyl)-2-trifluoromethyl-imidazo[1,2-a]pyridine (175) 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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524756B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-3106a978ac6f429cb40628565a7c5d19
Quellennotizuspto-grants-2013_09