Реакция #2146794

Уравнение реакции

2,4-dimethoxy-3-nitro-iodobenzene

4-ethynyl-1-methyl-1H-pyrazole

acetonitrile

→

title compound

Выход 71.0%

4-(2,4-Dimethoxy-3-nitro-phenylethynyl)-1-methyl-1H-pyrazole

Выход 71.0%

Растворители

triethylamine

Условия реакции

Обработка

1. 1
   workup.ADDITIONwere added under nitrogen atmosphere at room temperature
2. 2
   Другоеa consumption of the iodobenzene
3. 3
   ДругоеThe solvent was evaporated under reduced pressure
4. 4
   Другоеthe residue purified by flash column chromatography (silica gel; dichloromethane:ethyl acetate 9:1)

Методика

To a mixture of 2,4-dimethoxy-3-nitro-iodobenzene (0.95 mmol), 0.122 g (1.15 mmol) of 4-ethynyl-1-methyl-1H-pyrazole, 0.028 g (0.04 mmol) of dichlorobis (triphenylphosphine)palladium (H) and 8 mg (0.042 mmol) of copper (I) iodide 4 mL of anhydrous acetonitrile and 2 mL of triethylamine were added under nitrogen atmosphere at room temperature. The resulting mixture was stirred for 1 hour, when TLC indicated a consumption of the iodobenzene. The solvent was evaporated under reduced pressure and the residue purified by flash column chromatography (silica gel; dichloromethane:ethyl acetate 9:1) to give the title compound in 71% yield as creamy crystals. H1 NMR (CDCl3) 3.88(s, 3H, Me); 3.9 (s, 3H, OMe); 4.07 (s, 3H, OMe); 6.7 (d, 1H, CH, J=8.9 Hz); 7.44 (d, 1H, CH, J=8.9 Hz); 7.56 (s, 1H, CH pyr); 7.62 (s, 1H, CH pyr).

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