HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 3-{(4-Fluorophenyl)-[1-(3,4-difluorophenyl)ethylamino]methyl}phenylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | N-[(3-Nitrophenyl)-(4-fluorophenyl)methyl]-N-[1-(3,4-difluorophenyl)ethyl]amine | HCID 18334151 | — |
| Catalyst | Dichloronickel;hexahydrate | HCID 11791229 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-{(4-Fluorophenyl)-[1-(3,4-difluorophenyl)ethylamino]methyl}phenylamine | HCID 18334133 | 21% |
Reaction Steps
In a similar manner to that described in Example (15b), a solution of N-[(3-nitrophenyl)-(4-fluorophenyl)methyl]-N-[1-(3,4-difluorophenyl)ethyl]amine (3.0 g) [prepared as described in step (a) above] in methanol (10 ml), nickel chloride hexahydrate (3.69 g) and sodium borohydride (1.24 g) were reacted, and the reaction mixture was purified to afford isomer A of the title compound (630 mg) as a pale yellow oil and isomer B of the title compound (580 mg) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06329405B1 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-45d96bbef1f64f888a119509ab1d9799 |
| Source note | uspto-grants-2001_12 |