Reacción #9815

ord-f629534e45f24ca1b3eebffb5d964052

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    FiltraciónThe catalyst was filtered off
  2. 2
    Otrothe filtrate evaporated
  3. 3
    Otrothe residue chromatographed on silica

Procedimiento

0.917 g 6-Nitro-2,3-dihydro-benzo[1,4]oxathiine-4,4-dioxide (from g)) were hydrogenated in a mixture of 20 ml THF and 20 ml MeOH with 0.90 g 5% Pd—C at atmospheric hydrogen pressure for 90 min. at room temperature. The catalyst was filtered off, the filtrate evaporated and the residue chromatographed on silica to yield 370 mg of the title compound.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07091345B2uspto-grants-2006_08