HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 3-{[1-(3,5-Difluorophenyl)ethylamino]-(4-methoxyphenyl)methyl}-4-methoxyphenylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | N-[1-(3,5-Difluorophenyl)ethyl]-N-[(2-methoxy-5-nitrophenyl)-(4-methoxyphenyl)methyl]amine | HCID 18334175 | — |
| Catalyst | Dichloronickel;hexahydrate | HCID 11791229 | — |
| Product | 3-{[1-(3,5-Difluorophenyl)ethylamino]-(4-methoxyphenyl)methyl}-4-methoxyphenylamine | HCID 18334243 | — |
Reaction Steps
Following a reaction and purification procedure similar to those described in Example (59b), 1.75 g of N-[1-(3,5-difluorophenyl)ethyl]-N-[(2-methoxy-5-nitrophenyl)-(4-methoxyphenyl)methyl]amine [prepared as described in step (a) above], 2.24 g of nickel chloride hexahydrate and 651 mg of sodium borohydride were reacted, to obtain 471 mg of isomer A and 650 mg of isomer B of the title compound were obtained as a yellow oil and an orange solid, respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06329405B1 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-32aafad258e646bfb7c9aa5ee279e138 |
| Source note | uspto-grants-2001_12 |