Reaktion #53440

Reaktionsgleichung

6-bromopyrrolo[1,2-a]pyrazine-3-carboxylic acid hydrochloride

dihydrochloride

DIEA

HATU

→

N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-6-bromopyrrolo[1,2-a]pyrazine-3-carboxamide

Lösungsmittel

DMF

THF

Reaktionsbedingungen

Aufarbeitung

1. 1
   Einengenis concentrated to dryness under reduced pressure
2. 2
   SonstigeThe resulting material is absorbed to silica gel
3. 3
   Sonstigepurified with silica gel chromatography (9% MeOH/1%NH3OH/CH2Cl2 as the eluent)
4. 4
   Sonstigecrystallized from EtOH/acetone/Et2O
5. 5
   Sonstigeto give an off white spheres

Vorschrift

To a suspension of 6-bromopyrrolo[1,2-a]pyrazine-3-carboxylic acid hydrochloride (1.67 mmol), (R)-3-aminoquinulidine dihydrochloride (0.34 g, 1.67 mmol), DIEA (1.5 mL, 8.35 mmol) in DMF (20 mL) and THF (10 mL) is added HATU (0.64 g, 1.67 mmol). The resulting suspension is stirred for 16 h at which time it is concentrated to dryness under reduced pressure. The resulting material is absorbed to silica gel and purified with silica gel chromatography (9% MeOH/1%NH3OH/CH2Cl2 as the eluent) salted with fumeric acid, and crystallized from EtOH/acetone/Et2O to give an off white spheres. Yield 45%. HRMS (FAB) calcd. for C15H17BrN4O+H 349.0664, found 349.0647.

Quelle