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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 4-[4-(6'-Amino-[2,2';4',3'']terpyridin-5''-yl)-benzyl]-piperazine-1-carboxylic acid tert-butyl ester | HCID 68759293 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5''-(4-Piperazin-1-ylmethyl-phenyl)-[2,2';4',3'']terpyridin-6'-ylamine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08343966B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-3904a4d7db4e4e988e100a5d7bbd08ab |
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| Source note | uspto-grants-2013_01 |
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