HCID 13012106, Verbindung → HCID 178463288, Verbindung
Reaktionsgleichung
[ClH:1].[CH3:2][CH:3]([NH2:16])[C:4]1[CH:9]=[CH:8][C:7]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[CH:6][CH:5]=1.Cl.C[CH:19]([NH2:34])[C:20]1C=[CH:24][C:23](CCC2C=CC=CC=2)=[CH:22][CH:21]=1>>[ClH:1].[C:7]1([C:10]2[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH:8]=[CH:9][C:4]([CH:3]([N:16]=[C:19]2[CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][NH:34]2)[CH3:2])=[CH:5][CH:6]=1Komponenten
3
Versuchsvorschrift
Following essentially the same procedure described in Example IV above and substituting α-methyl-ρ-phenylbenzylamine hydrochloride for the α-methyl-ρ-phenethylbenzylamine hydrochloride above, results in the formation of 2-[α-(4-biphenylyl)ethylimino]hexahydroazepine hydrochloride having a M.P. of 245°-7° C.
Quellen und Nachweise
- ORD-Eintrag
- ord-5fbbcc71c3f645e9a3718eba653542d3
- Quelldatensatz
- uspto-grants-1977_10
- Patentnummer
- US04055561
Notizen zur Reaktion
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