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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1274684Generated: November 4, 2026

2-Benzylamino-4-(t-butyl)amino-3,5,6-trifluoropyridine → 2-Amino-4-(t-butylamino)-3,5,6-trifluoropyridine

https://huagongshe.com/reaction/1274684

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Benzylamino-4-(t-butyl)amino-3,5,6-trifluoropyridineHCID 22121267—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
Product2-Amino-4-(t-butylamino)-3,5,6-trifluoropyridineHCID 22121163—

Reaction Steps

To 13 ml of acetic acid were added 4.0 g of the crude 2-benzylamino-4-(t-butyl)amino-3,5,6-trifluoropyridine as described above together with 0.43 g of 10% palladium on carbon, and the mixture was hydrogenated at 60° C. for 6 hours. The catalyst was separated by filtration, and the solvent and the like were distilled off under reduced pressure to obtain the title compound as a brown crude oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06156903
Source datasetuspto-grants-2000_12
ORD IDord-1756e91a85ff43ae82d19c9831eb72aa
Source noteuspto-grants-2000_12