HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(diphenylmethyl) N-(2-nitrophenyl)-1-piperazinepropanamine hydrochloride → N-(2-aminophenyl)-4-(diphenylmethyl)-1-piperazinepropanamine hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(diphenylmethyl) N-(2-nitrophenyl)-1-piperazinepropanamine hydrochloride | HCID 20506361 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(2-aminophenyl)-4-(diphenylmethyl)-1-piperazinepropanamine hydrochloride | HCID 20506359 | — |
Reaction Steps
A mixture of 15 parts of 4-(diphenylmethyl) N-(2-nitrophenyl)-1-piperazinepropanamine hydrochloride in 160 parts of methanol is hydrogenated at normal pressure and at room temperature with 5 parts of Raney-nickel catalyst. After the calculated amount of hydrogen is taken up, the catalyst is filtered off over hyflo and the filtrate is evaporated. The solid residue is crystallized from a mixture of 2-propanol and 2,2'-oxybispropane. The product is filtered off and dried, yielding N-(2-aminophenyl)-4-(diphenylmethyl)-1-piperazinepropanamine hydrochloride; mp. 223.1° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04377578 |
| Source dataset | uspto-grants-1983_03 |
| ORD ID | ord-62b9dadea16f465c9243a7ff2c5d3de1 |
| Source note | uspto-grants-1983_03 |