Reacción #76740

ord-30e2de28c785469084b6ac0c29bbbeec

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe catalyst was removed by filtration
  2. 2
    Filtraciónthrough filter aid
  3. 3
    Concentraciónthe filtrate was concentrated
  4. 4
    workup.DISSOLUTIONThe residue was dissolved in water (10 mL)
  5. 5
    FiltraciónThe precipitate was collected by filtration
  6. 6
    Otropurified by preparative HPLC

Procedimiento

Propane-2-sulfonic acid 6-(2,4-diamino-pyrimidin-5-ylmethyl)-1-ethyl-3-morpholin-4-ylmethyl-1H-indol-4-yl ester (Example 10d; 270 mg, 0.55 mmol) was dissolved in methanol (50 mL) and 1 M aqueous hydrochloric acid solution (0.6 mL) and hydrogenated at room temperature and atmospheric pressure for 16 h in the presence of palladium on activated charcoal (10%, 170 mg). The catalyst was removed by filtration through filter aid and the filtrate was concentrated. The residue was dissolved in water (10 mL) and the pH set to ≈9 with 25% aqueous ammonia solution. The precipitate was collected by filtration and purified by preparative HPLC to afford the title compound (63 mg, 28%). Off-white solid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06703397B2uspto-grants-2004_03