1-(3-Aminopropyl)-4-methylpiperazine → [5-Chloro-4-(7-methoxybenzo[b]thiophen-2-yl)-pyrimidin-2-yl]-[3-(4-methyl-piperazin-1-yl)-propyl]-amine
Reaktionsgleichung
Cl.Cl.Cl.S1C(C2C=CN=C([NH:15][CH2:16][CH2:17][CH2:18][N:19]3[CH2:24][CH2:23][N:22]([CH3:25])[CH2:21][CH2:20]3)N=2)=CC2C=CC=CC1=2.Cl[C:31]1[N:36]=[C:35]([C:37]2[S:41][C:40]3[C:42]([O:46][CH3:47])=[CH:43][CH:44]=[CH:45][C:39]=3[CH:38]=2)[C:34]([Cl:48])=[CH:33][N:32]=1.NCCCN1CCN(C)CC1>>[Cl:48][C:34]1[C:35]([C:37]2[S:41][C:40]3[C:42]([O:46][CH3:47])=[CH:43][CH:44]=[CH:45][C:39]=3[CH:38]=2)=[N:36][C:31]([NH:15][CH2:16][CH2:17][CH2:18][N:19]2[CH2:20][CH2:21][N:22]([CH3:25])[CH2:23][CH2:24]2)=[N:32][CH:33]=1Komponenten
4
Edukt 3
Produkt 1
Versuchsvorschrift
Using the method of [4-(benzo[b]thiophen-2-yl)-pyrimidin-2-yl]-[3-(4-methylpiperazin-1-yl)-propyl]-amine tri-hydrochloride, the title compound is prepared from 2,5-dichloro-4-(7-methoxybenzo[b]thiophen-2-yl)-pyrimidine and 1-(3-aminopropyl)-4-methylpiperazine and isolated as a yellowish solid. ES+(m/z) 432(35Cl) and 434(37Cl) [M+H].
Aufarbeitung
- customisolated as a yellowish solid
Quellen und Nachweise
- ORD-Eintrag
- ord-e5d30b38bc48464db4d04380ac71369c
- Quelldatensatz
- uspto-grants-2009_06
- Patentnummer
- US07547691B2
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