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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1798495Generated: October 31, 2026

Tert-Butyl-[5''-(3-methoxy-phenyl)-[2,2';4',3'']terpyridin-6'-yl]-amine → 5''-(3-Methoxy-phenyl)-[2,2';4',3'']terpyridin-6'-ylamine

https://huagongshe.com/reaction/1798495

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-Butyl-[5''-(3-methoxy-phenyl)-[2,2';4',3'']terpyridin-6'-yl]-amineHCID 68736706—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
Product5''-(3-Methoxy-phenyl)-[2,2';4',3'']terpyridin-6'-ylamineHCID 44137102—

Reaction Conditions

Temperature70 °C

Reaction Steps

Tert-Butyl-[5″-(3-methoxy-phenyl)-[2,2′;4′,3″]terpyridin-6′-yl]-amine (1 eq, 0.073 mmol, 0.030 g) is dissolved in TFA (6 ml)/DCM (1 ml) and the reaction mixture is heated at 70° C. for 5 hours. The reaction mixture is cooled down and reduced in vacuo. The resulting residue is dissolved in MeOH and loaded onto a SCX-2 cartridge eluting with MeOH followed by 2M NH3 in MeOH. The methanolic ammonia fractions are combined, concentrated in vacuo and dried under vacuum to afford the title compound; [M+H]+ 355.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343966B2
Source datasetuspto-grants-2013_01
ORD IDord-9a57e2d39c1f4cbb98d2b27e7b90135d
Source noteuspto-grants-2013_01