HuagongsheHuagongshe Chemistry Print Report · For research reference only
2H-Azepine, 3,4,5,6-tetrahydro-7-methoxy- → HCID 178463314, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2H-Azepine, 3,4,5,6-tetrahydro-7-methoxy- | HCID 75657 | — |
| Reactant | 2-Methoxy-1-Pyrroline | HCID 353443 | — |
| Reactant | alpha-Methyl-p-phenethylbenzylamine hydrochloride | HCID 13012107 | — |
| Reactant | alpha-Methyl-m-(4-phenoxybutoxy)benzylamine hydrochloride | HCID 13012120 | — |
| Product | HCID 178463314 | HCID 178463314 | — |
Reaction Steps
Substituting this amine for the α-methyl-ρ-phenethylbenzylamine hydrochloride, and substituting O-methylbutyrolactim for the O-methylcaprolactim results in the formation of 2-[α-methyl-m-(4-phenoxybutoxy)benzylimino]pyrrolidine hydrochloride, having a M.P. of 136°-8° C. (dec.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04055561 |
| Source dataset | uspto-grants-1977_10 |
| ORD ID | ord-9cd90a0f9d434381b09ab01a259effce |
| Source note | uspto-grants-1977_10 |