Reaktionsgleichung
[N:1]1([CH2:7][C:8]2[CH:9]=[C:10]([CH:20]=[CH:21][CH:22]=2)[O:11][CH2:12][CH2:13][CH2:14][NH:15][C:16]([NH:18][NH2:19])=[S:17])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[CH:23]1([N:29]=[C:30]=[S:31])[CH2:28][CH2:27][CH2:26][CH2:25][CH2:24]1>>[CH:23]1([NH:29][C:30]([NH:19][NH:18][C:16](=[S:17])[NH:15][CH2:14][CH2:13][CH2:12][O:11][C:10]2[CH:20]=[CH:21][CH:22]=[C:8]([CH2:7][N:1]3[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]3)[CH:9]=2)=[S:31])[CH2:28][CH2:27][CH2:26][CH2:25][CH2:24]1Komponenten
3
Versuchsvorschrift
The compound is prepared by a method analogous to that of Example 5 from N-[3-[3-(1-piperidinylmethyl)phenoxy]propyl]hydrazine carbothioamide and cyclohexylisothiocyanate. The analytical values are summarized in Table I.
Quellen und Nachweise
- ORD-Eintrag
- ord-049983a7bc894ccd9b46d98e5ad2a72c
- Quelldatensatz
- uspto-grants-1988_02
- Patentnummer
- US04727081
Verknüpfte Notizen
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