HuagongsheHuagongshe Chemistry Print Report · For research reference only
N6-((4-Fluorophenyl)methyl)-3-nitropyridine-2,6-diamine → N~6~-[(4-Fluorophenyl)methyl]pyridine-2,3,6-triamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N6-((4-Fluorophenyl)methyl)-3-nitropyridine-2,6-diamine | HCID 118472 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | 2-Methoxyethanol | HCID 8019 | — |
| Product | N~6~-[(4-Fluorophenyl)methyl]pyridine-2,3,6-triamine | HCID 10868158 | — |
Reaction Steps
2-amino-3-nitro-6-(4-fluorobenzylamino)pyridine (ANFP) is dissolved in 2-methoxyethanol and is hydrogenated with hydrogen in the presence of Raney nickel at 5 bar and 60° C. to give 2,3-diamino-6-(4-fluorobenzyl-amino)pyridine. This is acylated with ethyl chloroformate and triethylamine under inert gas to give flupirtine base. The catalyst is filtered off and a solution of isopropanol and maleic acid is added directly to the filtrate which contains triethylamine hydrochloride, crude flupirtine maleate being precipitated with vigorous stirring under an inert-gas atmosphere.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05959115 |
| Source dataset | uspto-grants-1999_09 |
| ORD ID | ord-3b7372a6373a49299bbb1fde1f609d6c |
| Source note | uspto-grants-1999_09 |