HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 3-{[(R)-1-(3-Fluorophenyl)ethylamino]-(4-methoxyphenyl)methyl}phenylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | N-[(R)-1-(3-Fluorophenyl)ethyl]-N-[(4-methoxyphenyl)-(3-nitrophenyl)methyl]amine | HCID 70188098 | — |
| Catalyst | Dichloronickel;hexahydrate | HCID 11791229 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-{[(R)-1-(3-Fluorophenyl)ethylamino]-(4-methoxyphenyl)methyl}phenylamine | HCID 70189153 | — |
Reaction Steps
Following a similar procedure to that described in Example (59b), 15.08 g of N-[(R)-1-(3-fluorophenyl)ethyl]-N-[(4-methoxyphenyl)-(3-nitrophenyl)methyl]amine [prepared as described in step (a) above], 18.84 g of nickel chloride hexahydrate, 6.0 g of sodium borohydride and 150 ml of methanol were reacted, to obtain 787 mg and 605 mg of isomer A and isomer B of the title compound, respectively, each as a pale yellowish oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06329405B1 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-11dfe415ee3b490d88afe4cd970c2e1d |
| Source note | uspto-grants-2001_12 |