HCID 13012106, compound → HCID 178463288, compound

HRID 973171Notes

Reaction equation

HRID 973171 reaction equation
[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]=1

Participants

3

Reactant 2

HCID 13012106HCID 13012106, compoundHCID 13012107alpha-Methyl-p-phenethylbenzylamine hydrochloride

Product 1

HCID 178463288HCID 178463288, compound

Procedure

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.

Sources & evidence

ORD record
ord-5fbbcc71c3f645e9a3718eba653542d3
Source dataset
uspto-grants-1977_10
Patent number
US04055561

Reaction notes

Loading…