Reaktion #68949

ord-3a9d7cffadef40bfa1ba3e23272ac17b

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    WaschenIsolation by SPE on a MP-TsOH cartridge, eluting with 2N ammonia in methanol
  2. 2
    Einengenfollowed by concentration

Vorschrift

5-(1-(4-Methoxybenzyl)-1H-imidazo[4,5-c]pyridin-6-ylamino)pyrazine-2-carbonitrile (10.6 mg, 30 μmol) was treated with TFA at 80° C. over 30 minutes. Isolation by SPE on a MP-TsOH cartridge, eluting with 2N ammonia in methanol, followed by concentration, gave the title compound as a white solid (7.02 mg, 100%). 1H NMR (d6-DMSO, 400 MHz) δ 12.79 (br s, 1H), 10.85 (br s, 1H), 8.76 (s, 2H), 8.75 (s, 1H), 8.35 (s, 1H), 8.26 (s, 1H). LCMS (2) Rt=1.36 min; m/z (ESI+) 238 (MH+), (ESI−) 236 (M−H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08530468B2uspto-grants-2013_09