Reacción #3945

ord-11a5b9119d9941618a2c6738f74ed215

Ecuación de reacción

COc1cc(SC)ccc1-c1nc2c[nH][nH]c(=O)c-2n1
2-(2-methoxy-4-methylmercapto-phenyl)-5H-imidazo[4,5-d]pyridazin-4-one
OO
hydrogen peroxide
COc1cc(S(C)=O)ccc1-c1nc2c[nH][nH]c(=O)c-2n1
2-(2-Methoxy-4-methylsulfinyl-phenyl)-5H-imidazo[4,5-d]pyridazin-4-one

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.STIRRINGIt is then stirred until a precipitate
  2. 2
    Otrohas formed
  3. 3
    FiltraciónThis is subjected to suction filtration
  4. 4
    Otropurified by chromatography on silica gel [eluant: methylene chloride/ethanol (100:0 to 100:3)]

Procedimiento

An amount of 0.21 gm of 2-(2-methoxy-4-methylmercapto-phenyl)-5H-imidazo[4,5-d]pyridazin-4-one is suspended in 10 ml of glacial acetic acid and mixed with 0.08 ml of 30% hydrogen peroxide. The mixture is stirred for 24 hours at ambient temperature and poured onto 20 ml of ice water. It is then stirred until a precipitate has formed. This is subjected to suction filtration and purified by chromatography on silica gel [eluant: methylene chloride/ethanol (100:0 to 100:3)].

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04722929uspto-grants-1988_02