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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610203Generated: November 1, 2026

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

https://huagongshe.com/reaction/610203

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 numberUS05998436
Source datasetuspto-grants-1999_12
ORD IDord-673499357ed447fba402d0cc920ded5e
Source noteuspto-grants-1999_12