HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Benzylamino-4-(t-butyl)amino-3,5,6-trifluoropyridine → 2-Amino-4-(t-butylamino)-3,5,6-trifluoropyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Benzylamino-4-(t-butyl)amino-3,5,6-trifluoropyridine | HCID 22121267 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-Amino-4-(t-butylamino)-3,5,6-trifluoropyridine | HCID 22121163 | — |
Reaction Steps
To 13 ml of acetic acid were added 4.0 g of the crude 2-benzylamino-4-(t-butyl)amino-3,5,6-trifluoropyridine as described above together with 0.43 g of 10% palladium on carbon, and the mixture was hydrogenated at 60° C. for 6 hours. The catalyst was separated by filtration, and the solvent and the like were distilled off under reduced pressure to-obtain the title compound as a brown crude oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06133284 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-99bdd0e5efa044ae9a4063ece55320d9 |
| Source note | uspto-grants-2000_10 |