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HRID 539573作成日:2026年10月26日

Potassium Carbonate → Methyl 3-(4-(trifluoromethyl)phenyl)pyrazolo[1,5-a]pyridine-5-carboxylate

https://huagongshe.com/reaction/539573

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物O-(2,4-dinitrophenyl)hydroxylamineHCID 87140—
反応物Methyl isonicotinateHCID 227085—
反応物1-Ethynyl-4-(trifluoromethyl)benzeneHCID 4348295—
溶媒DimethylformamideHCID 6228—
生成物Methyl 3-(4-(trifluoromethyl)phenyl)pyrazolo[1,5-a]pyridine-5-carboxylateHCID 8672025325%

反応条件

温度40 °C

反応手順

To a solution of methyl isonicotinate (500 μL, 4.23 mmol, 1.0 equiv.) in 2 mL DMF was added O-(2,4-dinitrophenyl)hydroxylamine (1 g, 5.02 mmol, 1.2 equiv.) and the resulting solution was allowed to stir overnight at 40° C., during which time the reaction became heterogeneous. The mixture was allowed to cool to rt before being diluted with 10 mL DMF, then treated with 4-ethynyl-α,α,α-trifluorotoluene (863 μL, 5.29 mmol, 1.25 equiv.) and potassium carbonate (877 mg, 6.35 mmol, 1.5 equiv.). The mixture was allowed to stir overnight at 100° C. The resulting mixture was allowed to cool to rt, and then the solvent was removed under reduced pressure. The residue was diluted with water and the aqueous layer was extracted with EtOAc five times. The combined EtOAc extracts were washed once with water, once with brine, and then dried with MgSO4, filtered, and the solvent removed under reduced pressure. The material was purified by silica gel chromatography, eluting with hexanes/EtOAc (Rf=0.26 in 5:1 hexanes/EtOAc) to give 335 mg (25% yield) I-1. 1H NMR (400 MHz, CDCl3, δ): 8.52 (m, 2H), 8.23 (s, 1H), 7.72 (s, 4H), 7.40 (dd, J=1.59, 7.50 Hz, 1H), 3.96 (s, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08871754B2
出典データセットuspto-grants-2014_10
ORD IDord-e9b8372471394a22b0735f64588b92d5
出典メモuspto-grants-2014_10