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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1798534Generated: October 30, 2026

Trifluoroacetic acid → 5''-(4-Piperazin-1-ylmethyl-phenyl)-[2,2';4',3'']terpyridin-6'-ylamine

https://huagongshe.com/reaction/1798534

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant4-[4-(6'-Amino-[2,2';4',3'']terpyridin-5''-yl)-benzyl]-piperazine-1-carboxylic acid tert-butyl esterHCID 68759293—
SolventDichloromethaneHCID 6344—
Product5''-(4-Piperazin-1-ylmethyl-phenyl)-[2,2';4',3'']terpyridin-6'-ylamineHCID 68758547—

Reaction Steps

To a solution of 4-[4-(6′-Amino-[2,2′;4′,3″]terpyridin-5″-yl)-benzyl]-piperazine-1-carboxylic acid tert-butyl ester (1.0 eq, 0.105 mmol, 55.1 mg) in DCM (1.0 ml) is added TFA (24.0 eq, 2.60 mmol, 0.2 ml). The reaction mixture is allowed to stir at room temperature for 30 minutes. The organic solvent is reduced in vacuo. The residue is purified by reverse phase chromatography (Isolute™ C18, 0-20% acetonitrile in water—0.1% TFA). The appropriate fractions by HPLC are combined and concentrated in vacuo. The resulting residue is dissolved in MeOH and loaded onto a SCX-2 cartridge eluting with MeOH and 2M NH3 in MeOH. The methanolic ammonia fractions are combined, concentrated in vacuo and dried under vacuum to afford the title compound; [M+H]+ 423.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343966B2
Source datasetuspto-grants-2013_01
ORD IDord-3904a4d7db4e4e988e100a5d7bbd08ab
Source noteuspto-grants-2013_01