Reacción #40702

ord-a5e9cfcf879a480fa44c407279407e0b

Ecuación de reacción

Cc1ccc(=O)n(-c2ccccc2)c1
1-phenyl-5-methyl-2-pyridinone
COc1ccc(P2(=S)SP(=S)(c3ccc(OC)cc3)S2)cc1
Lawesson's reagent
Cc1ccc(=S)n(-c2ccccc2)c1
1-phenyl-5-methyl-2-pyridinethione

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroReaction mixture
  2. 2
    Otrowas evaporated
  3. 3
    Otrothe target compound was isolated by column chromatography (20-30% ethyl acetate-hexane)
  4. 4
    Otrofollowed by crystallization from methyl-tert-butyl ether

Procedimiento

1-phenyl-5-methyl-2-pyridinone (555.7 mg, 3 mmol) was reacted with Lawesson's reagent (606.7 mg, 1.5 mmol) in toluene (5 ml) at 90° C. Reaction mixture was evaporated and the target compound was isolated by column chromatography (20-30% ethyl acetate-hexane) followed by crystallization from methyl-tert-butyl ether. Yield 403 mg (67%), yellow solid. The 1H NMR spectra was consistent with the structure of Compound 18.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07728013B2uspto-grants-2010_06