Reaktionsgleichung
[CH2:1]([S:8][C:9]1[CH:15]=[CH:14][CH:13]=[CH:12][C:10]=1[NH2:11])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:16](Cl)(=[O:25])[CH:17]=[CH:18][C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1.C(SC1C=CC=CC=1C[C:42]([NH:44][C:45]1[CH:50]=[CH:49][CH:48]=[CH:47]C=1)=O)C1C=CC=CC=1.Br[CH2:52]CCCCBr>>[CH3:52][N:44]([CH3:42])[CH2:45][CH2:50][CH2:49][CH2:48][CH2:47][N:11]([C:10]1[CH:12]=[CH:13][CH:14]=[CH:15][C:9]=1[S:8][CH2:1][C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1)[C:16](=[O:25])[CH:17]=[CH:18][C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1Komponenten
5
Versuchsvorschrift
Following the method described in Example 5 but substituting the product of the reaction of 2-(benzylthio)aniline and cinnamoyl chloride for the 2-(benzylthio)phenylacetanilide and using 1,5-dibromopentane in place of 1,4-dibromobutane, the title compound is obtained. This material was isolated as a pale yellow oil.
Quellen und Nachweise
- ORD-Eintrag
- ord-2b3400f1ae9f425ba62aa5ae032b800c
- Quelldatensatz
- uspto-grants-1992_05
- Patentnummer
- US05116851
Verknüpfte Notizen
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