Reaktion #53443

ord-35777fbdf51d4a96b2a0653b70a174ab

Reaktionsbedingungen

Temperatur
95°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Filtrationfiltered through a pad of celite
  2. 2
    SonstigeThe residue is purified
  3. 3
    Sonstigeto give a pale yellow oil that
  4. 4
    Sonstigecrystallized from EtOH/Et2O
  5. 5
    Sonstigeto give a pale yellow solid

Vorschrift

To an argon sparged solution of N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-6-bromopyrrolo[1,2-a]pyrazine-3-carboxamide (0.77 g, 2.14 mmol) in DMF (25 mL) is added zinc cyanide (0.26 g, 2.20 mmol), and tetrakis(triphenylphosphine)palladium (0) (0.25 g, 0.21 mmol). The resulting suspension is stirred at 95° C. for 48 h, then filtered through a pad of celite. The residue is purified using preparative chromatography (carried out on a Chiral OD column using a 40% IPA/heptanes each containing 0.1% diethylamine) to give a pale yellow oil that is salted with d-tartaric acid and crystallized from EtOH/Et2O to give a pale yellow solid. Yield 47%. HRMS (FAB) calcd for C16H17N5O+H 296.1511, found 296.1520.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06858613B2uspto-grants-2005_02