HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Benzylamino-4-(t-butylamino)-5-fluoropyrimidine → 2-Amino-4-(t-butylamino)-5-fluoropyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Benzylamino-4-(t-butylamino)-5-fluoropyrimidine | HCID 22121262 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-Amino-4-(t-butylamino)-5-fluoropyrimidine | HCID 22121290 | 53.6% |
Reaction Steps
To 8 ml of acetic acid were added 1.00 g of 2-benzylamino-4-(t-butylamino)-5-fluoropyrimidine together with 215 mg of 10% palladium on carbon, and the mixture was hydrogenated at 60° C. for ten days. The catalyst was separated by filtration, and the solvent and the like were distilled off under reduced pressure. The procedure of adding 10 ml of ethanol and concentrating under reduced pressure was repeated three times, and the residue was separated by column chromatography (silica gel, 25 g; eluent: chloroform, and then, chloroform:methanol, 200:1), and the corresponding fractions were collected and concentrated under reduced pressure to obtain 360 mg of the title compound as a pale gray solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06133284 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-5c70b95625d54b51b6e3c135d993c3e4 |
| Source note | uspto-grants-2000_10 |