HCID 24774027, Verbindung → HCID 59985812, Verbindung
Reaktionsgleichung
Cl.[CH:2]1[C:3]2[N:4]([CH:11]=[CH:12][CH:13]=2)[CH:5]=[C:6]([C:8]([OH:10])=O)[N:7]=1.Cl.Cl.[N:16]12[CH2:23][C@H:20]([CH2:21][CH2:22]1)[CH2:19][C@@H:18]([NH2:24])[CH2:17]2>>[N:16]12[CH2:23][C@H:20]([CH2:21][CH2:22]1)[CH2:19][C@@H:18]([NH:24][C:8]([C:6]1[N:7]=[CH:2][C:3]3[N:4]([CH:11]=[CH:12][CH:13]=3)[CH:5]=1)=[O:10])[CH2:17]2Komponenten
3
Versuchsvorschrift
Example 15 is prepared from pyrrolo[1,2-a]pyrazine-3-carboxylic acid hydrochloride and (3R,5R)-1-azabicyclo[3.2.1]octan-3-amine dihydrochloride using Procedure C to give a mixture purified by silica gel chromatography (9% MeOH/1%NH3OH/CHCl3 as the eluent) salted with fumaric acid, and crystallized from acetone to give a white solid. Yield 83%. HRMS (FAB) calcd for C15H18N4O MH+271.1559, found 271.1550.
Aufarbeitung
- customto give a mixture
- custompurified by silica gel chromatography (9% MeOH/1%NH3OH/CHCl3 as the eluent)
- customcrystallized from acetone
- customto give a white solid
Quellen und Nachweise
- ORD-Eintrag
- ord-f4a2806e6c3941c7818c5630489ed9e7
- Quelldatensatz
- uspto-grants-2005_02
- Patentnummer
- US06858613B2
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