Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 368428Generated: October 30, 2026

2-Benzylamino-4-(t-butylamino)-5-fluoropyrimidine → 2-Amino-4-(t-butylamino)-5-fluoropyrimidine

https://huagongshe.com/reaction/368428

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Benzylamino-4-(t-butylamino)-5-fluoropyrimidineHCID 22121262—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
Product2-Amino-4-(t-butylamino)-5-fluoropyrimidineHCID 2212129053.6%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06133284
Source datasetuspto-grants-2000_10
ORD IDord-5c70b95625d54b51b6e3c135d993c3e4
Source noteuspto-grants-2000_10