HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Cyanobenzaldehyde → N-{3-[N-(3-aminopropyl)-N-metylamino]propyl}-2-(p-chlorophenyl)ethylamine trihydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Cyanobenzaldehyde | HCID 66042 | — |
| Reactant | 2-(4-Chlorophenyl)acetaldehyde | HCID 11412502 | — |
| Reactant | N-{3-[N-(3-aminopropyl)-N-methylamino]propyl}-p-cyanobenzylamine trihydrochloride | HCID 20407117 | — |
| Product | N-{3-[N-(3-aminopropyl)-N-metylamino]propyl}-2-(p-chlorophenyl)ethylamine trihydrochloride | HCID 20407063 | 51% |
Reaction Steps
In a similar manner to that described above, N-{3-[N-(3-aminopropyl)-N-methylamino]propyl}-p-cyanobenzylamine trihydrochloride (81% yeild) and N-{3-[N-(3-aminopropyl)-N-metylamino]propyl}-2-(p-chlorophenyl)ethylamine trihydrochloride (51% yield) were obtained from p-cyanobenzaldehyde and p-chlorophenylacetaldehyde, respectively. The physicohemical properties of these compounds were as shown in Table 8.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04472304 |
| Source dataset | uspto-grants-1984_09 |
| ORD ID | ord-dccc6f69482b47b188458ec414f94d77 |
| Source note | uspto-grants-1984_09 |