HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 368446Generated: October 29, 2026
Hydrochloric Acid → 2-Amino-6-(t-butylamino)-5-fluoropyridine
https://huagongshe.com/reaction/368446
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-Benzylamino-6-(t-butylamino)-3-chloro-5-fluoropyridine | HCID 22121183 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Amino-6-(t-butylamino)-5-fluoropyridine | HCID 22121230 | — |
| Product | 2-Amino-6-(t-butylamino)-3-chloro-5-fluoropyridine | HCID 22121249 | — |
Reaction Steps
To a mixed solution of 18 ml methanol and 1.4 g concentrated hydrochloric acid were added 3.1 g of 20 2-benzylamino-6-(t-butylamino)-3-chloro-5-fluoropyridine together with 0.33 g of 10% palladium on carbon, and the mixture was hydrogenated at 30° C. for 1 hour. The catalyst was separated by filtration, and the solvent and the like were distilled off under reduced pressure. To the residue was added 50 ml of chloroform, and the mixture was washed with 10 ml of 6% aqueous solution of sodium hydroxide, and the chloroform layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was subjected to column chromatography (silica gel, 40 g; eluent: chloroform:n-hexane, 3:1 and then 1:1) to obtain 1.35 g of 2-amino-6-(t-butylamino)-3-chloro-5-fluoropyridine as a pale brown oil, and 0.32 g of 2-amino-6-(t-butylamino)-5-fluoropyridine as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06133284 |
|---|
| Source dataset | uspto-grants-2000_10 |
|---|
| ORD ID | ord-0850b0360d504aeab40dc6e2526bb79c |
|---|
| Source note | uspto-grants-2000_10 |
|---|