Pyrazole → 1-[5-(3,5-Dichloro-phenyl)-5-trifluoromethyl-4,5-dihydro-isoxazol-3-yl]-1H-pyrazole-3-carboxylic acid methyl ester

To a solution of pyrazole-3-carboxylic acid methyl ester (504 mg) in acetonitrile (25 ml) under argon was added sodium hydride (160 mg). The reaction mixture was stirred at room temperature for 1 h. 15 mf of this solution was added dropwise to a solution of chloroisoxazoline of example 17.2 (630 mg) in acetonitrile (10 ml). It was then stirred at room temperature for 1 h; 10 ml of pyrazole solution was added again and the mixture was stirred for 1.5 hour. The reaction was quenched by adding water and dichloromethane. The two layers were separated. The aqueous layer was extracted with dichloromethane. The combined organic layers were washed with brine, dried over sodium sulfate and concentrated. The crude residue was purified by column chromatography (from c-Hex (100%) to c-Hex:EtOAc (80:20)) to afford the title intermediate (680 mg). 1H-NMR (CDCl3, 400 MHz): 8.15 (s, 1H), 7.5 (m, 2H), 7.45 (m, 1H), 4.45 (d, 1H), 4.10 (d, 1H), 3.95 (s, 3H).

1. stirringIt was then stirred at room temperature for 1 h
2. stirringthe mixture was stirred for 1.5 hour
3. customThe reaction was quenched
4. additionby adding water and dichloromethane
5. customThe two layers were separated
6. extractionThe aqueous layer was extracted with dichloromethane
7. washThe combined organic layers were washed with brine
8. dry with materialdried over sodium sulfate
9. concentrationconcentrated
10. customThe crude residue was purified by column chromatography (from c-Hex (100%) to c-Hex:EtOAc (80:20))

ORD record

ord-82bd5e286454424e9042eabc1fe637b3

Source dataset

uspto-grants-2015_12

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US09216973B2