Dodecylamine → HCID 20287139, Verbindung
Reaktionsgleichung
[CH2:1]([NH2:13])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12].[ClH:14].CC(C)(C)CN[C:19](=[O:43])[C:20]1[CH:25]=[C:24]([CH:26]([OH:41])[CH2:27][N:28]2[CH2:33][CH2:32][N:31]([C:34]3[CH:39]=[CH:38][CH:37]=[CH:36][C:35]=3[CH3:40])[CH2:30][CH2:29]2)[CH:23]=[CH:22][C:21]=1[OH:42]>>[ClH:14].[CH2:1]([NH:13][C:19](=[O:43])[C:20]1[CH:25]=[C:24]([CH:26]([OH:41])[CH2:27][N:28]2[CH2:29][CH2:30][N:31]([C:34]3[CH:39]=[CH:38][CH:37]=[CH:36][C:35]=3[CH3:40])[CH2:32][CH2:33]2)[CH:23]=[CH:22][C:21]=1[OH:42])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12]Komponenten
3
Versuchsvorschrift
Following essentially the same procedure but substituting dodecylamine for the neopentylamine above results in the preparation of N-dodecyl-2-hydroxy-5-[1-hydroxy-2-[4-(2-methylphenyl)-1-piperazinyl]ethyl]benzamide hydrochloride.
Quellen und Nachweise
- ORD-Eintrag
- ord-cd5de87adc664514a78812db4d9ff94a
- Quelldatensatz
- uspto-grants-1981_03