Reaktionsgleichung
C(N1CCNCC1)=O.[C:9]12([N:19]3[CH2:24][CH2:23][NH:22][CH2:21][CH2:20]3)[CH2:18][CH:13]3[CH2:14][CH:15]([CH2:17][CH:11]([CH2:12]3)[CH2:10]1)[CH2:16]2.[IH:25].CS[C:28](=[NH:30])[NH2:29]>>[IH:25].[C:9]12([N:19]3[CH2:24][CH2:23][N:22]([C:28](=[NH:29])[NH2:30])[CH2:21][CH2:20]3)[CH2:16][CH:15]3[CH2:14][CH:13]([CH2:12][CH:11]([CH2:17]3)[CH2:10]1)[CH2:18]2Komponenten
4
Versuchsvorschrift
The title compound was prepared as described for 1-formylpiperazine in Example 1 of the published European patent application No. 39,190, starting with 1-(1-adamantyl)piperazine and S-methyl-isothiourea hydroiodide, mp. 278°-280° C., yield: 72.3 %.
Quellen und Nachweise
- ORD-Eintrag
- ord-73472acde6f74bd990200d27ffc51b80
- Quelldatensatz
- uspto-grants-1995_01
- Patentnummer
- US05380724
Verknüpfte Notizen
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