HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 3-{[(R)-1-(3,5-Difluorophenyl)ethylamino]-(4-fluorophenyl)methyl}phenylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | N-[(R)-1-(3,5-Difluorophenyl)ethyl]-N-[(4-fluorophenyl)-(3-nitrophenyl)methyl]amine | HCID 70189758 | — |
| Catalyst | Dichloronickel;hexahydrate | HCID 11791229 | — |
| Product | 3-{[(R)-1-(3,5-Difluorophenyl)ethylamino]-(4-fluorophenyl)methyl}phenylamine | HCID 70189768 | — |
Reaction Steps
Following a reaction and purification procedure similar to those described in Example (59b), 4.40 g of N-[(R)-1-(3,5-difluorophenyl)ethyl]-N-[(4-fluorophenyl)-(3-nitrophenyl)methyl]amine [prepared as described in step (a) above], 6.54 g of nickel chloride hexahydrate and 1.81 g of sodium borohydride were reacted, to obtain 1.24 g of isomer A and 1.66 g of isomer B of the title compound as yellow oils, respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06329405B1 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-5cc33074077446558967c770e935ac58 |
| Source note | uspto-grants-2001_12 |