Réaction #1909

Équation de réaction

product

3-cyano-4-trifluoromethylsulfenyl-5-(N-trifluoroacetylamino)pyrazole

ammonium hydroxide

hydrochloric acid

→

title compound

Rendement 87.6%

3-cyano-4-trifluoromethylsulfenyl-5-aminopyrazole

Rendement 87.6%

Solvants

methanol

ethyl acetate

Conditions de réaction

Traitement

1. 1
   Températurethe solution was refluxed for 3 hours
2. 2
   LavageThe organic layer was washed several times with water and brine
3. 3
   Séchagedried over MgSO4
4. 4
   Concentrationconcentrated to dryness
5. 5
   Autreto give an oily brown residue which
6. 6
   Autrewas recrystallized from methyl tert-butyl ether

Mode opératoire

The product of Step E (55 g, 181 mmoles) was dissolved in methanol. 100 ml of ammonium hydroxide were added, the solution was refluxed for 3 hours and then stirred at room temperature for 15 hours. The methanolic solution was brought to pH7 using concentrated aqueous hydrochloric acid and diluted with ethyl acetate. The organic layer was washed several times with water and brine, dried over MgSO4 and concentrated to dryness to give an oily brown residue which was recrystallized from methyl tert-butyl ether to afford 33 g of the title compound, m.p. around 187° C.

Source