Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Benzylamino-6-(t-butylamino)-3-chloro-5-fluoropyridineHCID 22121183—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product2-Amino-6-(t-butylamino)-5-fluoropyridineHCID 22121230—
Product2-Amino-6-(t-butylamino)-3-chloro-5-fluoropyridineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06133284
Source datasetuspto-grants-2000_10
ORD IDord-0850b0360d504aeab40dc6e2526bb79c
Source noteuspto-grants-2000_10