Potassium Carbonate → N1-Cinnamyl-N4-[1-(5-chloro-6-methoxy-2-naphthoyl)ethyl]piperazine dihydrochloride
Reaktionsgleichung
[ClH:1].Cl.[CH2:3]([N:12]1[CH2:17][CH2:16][NH:15][CH2:14][CH2:13]1)[CH:4]=[CH:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.Br[CH:19]([CH3:35])[C:20]([C:22]1[CH:31]=[CH:30][C:29]2[C:24](=[CH:25][CH:26]=[C:27]([O:33][CH3:34])[C:28]=2[Cl:32])[CH:23]=1)=[O:21].C([O-])([O-])=O.[K+].[K+]>C(Cl)(Cl)Cl>[ClH:32].[ClH:1].[CH2:3]([N:12]1[CH2:17][CH2:16][N:15]([CH:19]([C:20]([C:22]2[CH:31]=[CH:30][C:29]3[C:24](=[CH:25][CH:26]=[C:27]([O:33][CH3:34])[C:28]=3[Cl:32])[CH:23]=2)=[O:21])[CH3:35])[CH2:14][CH2:13]1)[CH:4]=[CH:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of N-cinnamyl piperazine dihydrochloride (2.75 g, 10 mmol), 2-bromo-1-(5-chloro-6-methoxynaphthalen-2-yl)propan-1-one (1.05 g, 3.2 mmol) and K2CO3 (1.3 g, 9.5 mmol) in 50 ml of CHCl3 was treated according to general preparation 2 to give 3.65 g of compound (IV-35), yield 70%. M+ 449.
Aufarbeitung
- additionwas treated
- customaccording to general preparation 2
Quellen und Nachweise
- ORD-Eintrag
- ord-8cedec75ec614abca71637cf6c11a06f
- Quelldatensatz
- uspto-grants-2008_02
- Patentnummer
- US07332495B2
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