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

温度

40 °C

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).

1. temperatureto cool to rt
2. stirringto stir overnight at 100° C
3. temperatureto cool to rt
4. customthe solvent was removed under reduced pressure
5. additionThe residue was diluted with water
6. extractionthe aqueous layer was extracted with EtOAc five times
7. washThe combined EtOAc extracts were washed once with water, once with brine
8. dry with materialdried with MgSO4
9. filtrationfiltered
10. customthe solvent removed under reduced pressure
11. customThe material was purified by silica gel chromatography
12. washeluting with hexanes/EtOAc (Rf=0.26 in 5:1 hexanes/EtOAc)
13. customto give 335 mg (25% yield) I-1

ORDレコード

ord-e9b8372471394a22b0735f64588b92d5

出典データセット

uspto-grants-2014_10

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US08871754B2