Reaktionsgleichung
[NH2:1][CH2:2][CH2:3][CH2:4][N:5]([CH3:10])[CH2:6][CH2:7]CN.[CH3:11][N:12](CCCN)[CH2:13][CH2:14][CH2:15][NH:16][C:17]1[C:30]2[C:29](=[O:31])[C:28]3[C:23](=[CH:24][CH:25]=[C:26]([F:32])[CH:27]=3)[NH:22][C:21]=2[C:20]([N+:33]([O-:35])=[O:34])=[CH:19][CH:18]=1.NCCN1CCN(CCN)CC1.NCCN1CCN(CCNC2C3C(=O)C4C(=CC=C(F)C=4)NC=3C([N+]([O-])=O)=CC=2)CC1>>[NH2:1][CH2:2][CH2:3][CH2:4][N:5]1[CH2:10][CH2:11][N:12]([CH2:13][CH2:14][CH2:15][NH:16][C:17]2[C:30]3[C:29](=[O:31])[C:28]4[C:23](=[CH:24][CH:25]=[C:26]([F:32])[CH:27]=4)[NH:22][C:21]=3[C:20]([N+:33]([O-:35])=[O:34])=[CH:19][CH:18]=2)[CH2:7][CH2:6]1Komponenten
5
Edukt 4
Produkt 1
Versuchsvorschrift
Beginning with N,N-bis(3 -aminopropyl)methylamine, 1-{3-[methyl(3-aminopropyl)amino]propyl}amino-7-fluoro-4-nitro-10H-acridin-9-one (compound 2c) is prepared by the above method. By the same method, but beginning with 1,4-bis(2-aminoethyl)piperazine, it is possible to prepare 1-{2-[4-(2-aminoethyl)piperazin-1-yl]ethyl}amino-7-fluoro-4-nitro-10H-acridin-9-one.
Aufarbeitung
- customis prepared by the above method
Quellen und Nachweise
- ORD-Eintrag
- ord-c6b2c0ee5770403cb5b7b0800cd572fa
- Quelldatensatz
- uspto-grants-2003_12
- Patentnummer
- US06664263B2
Verknüpfte Notizen
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