Réaction #157160

ord-fe0e47b5fef745d2b833bc1b4dfba5f8

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe Boc protected product was purified by preparative HPLC
  2. 2
    AutreAfter volatile materials were removed
  3. 3
    AutreAfter volatile materials were removed in vacuo

Mode opératoire

Method 2 of Example 49 was followed using 3-amino-N-(4-((S)-3-aminopiperidin-1-yl)pyridin-3-yl)-6-(3-(benzyloxy)-2,6-difluorophenyl)-5-fluoropicolinamide with 20 wt % Pd/C in methanol (0.1 M solution). The Boc protected product was purified by preparative HPLC. After volatile materials were removed, the crude material was stirred in 30% TFA in dichloromethane. After volatile materials were removed in vacuo, 3-amino-N-(4-((S)-3-aminopiperidin-1-yl)pyridin-3-yl)-6-(2,6-difluoro-3-hydroxyphenyl)-5-fluoropicolinamide was obtained by preparative HPLC. LCMS (m/z): 459.2 (MH+); LC Rt=2.10 min.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08822497B2uspto-grants-2014_09