HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 13012106, compound → HCID 178463288, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 13012106 | HCID 13012106 | — |
| Reactant | alpha-Methyl-p-phenethylbenzylamine hydrochloride | HCID 13012107 | — |
| Product | HCID 178463288 | HCID 178463288 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04055561 |
| Source dataset | uspto-grants-1977_10 |
| ORD ID | ord-5fbbcc71c3f645e9a3718eba653542d3 |
| Source note | uspto-grants-1977_10 |