Réaction #531827

Équation de réaction

2-[3-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazol-5-yl]-6-iodo-8-methyl-4H-3,1-benzoxazin-4-one

benzoxazinone

2-[3-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazol-5-yl]-6-iodo-8-methyl-4H-3,1-benzoxazin-4-one

copper(I) cyanide

→

title compound

2-[3-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazol-5-yl]-6-cyano-8-methyl-4H-3,1-benzoxazin-4-one

Solvants

ethyl acetate

tetrahydrofuran

Conditions de réaction

Traitement

1. 1
   TempératureThe reaction mixture was then heated
2. 2
   Températureat reflux overnight
3. 3
   AutreThe reaction turned black in color, at which point thin layer chromatography on silica gel confirmed completion of the reaction
4. 4
   Filtrationfiltered through Celite®
5. 5
   Lavageby washing three times with 10% sodium bicarbonate solution
6. 6
   ExtractionThe organic extract
7. 7
   Séchagewas dried (MgSO4)
8. 8
   Concentrationconcentrated under reduced pressure

Mode opératoire

To a solution of 2-[3-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazol-5-yl]-6-iodo-8-methyl-4H-3,1-benzoxazin-4-one (i.e. the benzoxazinone product of Step E) (600 mg, 1.1 mmol) in tetrahydrofuran (15 mL) was added copper(I) iodide (126 mg, 0.66 mmol), tetrakis(triphenyphosphine)palladium(0) (382 mg, 0.33 mmol) and copper(I) cyanide (800 mg, 8.8 mmol) sequentially at room temperature. The reaction mixture was then heated at reflux overnight. The reaction turned black in color, at which point thin layer chromatography on silica gel confirmed completion of the reaction. The reaction mixture was diluted with ethyl acetate (20 mL) and filtered through Celite®, followed by washing three times with 10% sodium bicarbonate solution and once with brine. The organic extract was dried (MgSO4) and concentrated under reduced pressure to afford 440 mg of the title compound as a crude yellow solid.

Source