Reaktionsgleichung
C1(SCC2[C:18]3[C:13](=[CH:14][CH:15]=[C:16](C4C=CC=CC=4OC)[CH:17]=3)[NH:12]C(C)(C)C=2)CCCCC1.Br[CH2:30][C:31]1[C:40]2[C:35](=[CH:36][CH:37]=[C:38]([C:41]3[CH:46]=[CH:45][CH:44]=[CH:43][C:42]=3[O:47][CH3:48])[CH:39]=2)[NH:34][C:33]([CH3:50])([CH3:49])[CH:32]=1.C(=O)([O-])[O-].[K+].[K+].C1(S)CCCCC1>>[CH3:48][O:47][C:42]1[CH:43]=[CH:44][CH:45]=[CH:46][C:41]=1[C:38]1[CH:39]=[C:40]2[C:35](=[CH:36][CH:37]=1)[NH:34][C:33]([CH3:50])([CH3:49])[CH:32]=[C:31]2[CH2:30][NH:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1Komponenten
5
Edukt 4
Produkt 1
Versuchsvorschrift
4-Cyclohexylsulfanylmethyl-6-(2-methoxyphenyl)-2,2-dimethyl-1,2-dihydroquinoline 60 mg of 4-bromomethyl-6-(2-methoxyphenyl)-2,2-dimethyl-1,2-dihydroquinoline, 46 mg of potassium carbonate, and 27 μL of cyclohexylmercaptan reacted to give 5 mg of the title compound as an oil.
Quellen und Nachweise
- ORD-Eintrag
- ord-4a5b08e9befb45b1b800a02c60dc6d92
- Quelldatensatz
- uspto-grants-2005_02
- Patentnummer
- US06858627B2
Verknüpfte Notizen
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