Reacción #157359

ord-0e9a93217bcd4a3694aa50d8713347e7

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Filtraciónthe reaction mixture was filtered
  2. 2
    Concentraciónconcentrated under reduced pressure
  3. 3
    OtroThe material was purified by HPLC (5 to 50% MeCN/0.1% TFA in H2O/0.1% TFA gradient)

Procedimiento

A solution of tert-butyl 4-(2-chlorooxazole-4-carbonyl)-3-((pyridin-3-yloxy)methyl)piperazine-1-carboxylate (117 mg, 0.277 mmol), aniline (51 mg, 0.554 mmol) and potassium carbonate (76 mg, 0.554 mmol) in THF (2 mL) was heated to 70° C. overnight. Upon cooling to rt, the reaction mixture was filtered and concentrated under reduced pressure. The material was purified by HPLC (5 to 50% MeCN/0.1% TFA in H2O/0.1% TFA gradient), yielding 64.8 mg (40%) of the title compound as the TFA salt. LC-MS: RT=6.72 min, [M+H]+=480.0.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08822472B2uspto-grants-2014_09