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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356339Generated: October 31, 2026

6-Methoxy-1,5-naphthyridin-4-yl trifluoromethanesulfonate → 2-(2-{4-[6-(methyloxy)-1,5-naphthyridin-4-yl]-2-oxo-1-piperazinyl}ethyl)-1H-isoindole-1,3(2H)-dione

https://huagongshe.com/reaction/2356339

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Methoxy-1,5-naphthyridin-4-yl trifluoromethanesulfonateHCID 11255265—
Reactant2-[2-(2-oxo-1-piperazinyl)ethyl]-1H-isoindole-1,3(2H)-dioneHCID 68453334—
SolventEthanolHCID 702—
Product2-(2-{4-[6-(methyloxy)-1,5-naphthyridin-4-yl]-2-oxo-1-piperazinyl}ethyl)-1H-isoindole-1,3(2H)-dioneHCID 6845551442.1%

Reaction Steps

A solution of 6-(methyloxy)-1,5-naphthyridin-4-yl trifluoromethanesulfonate (169 mg, 0.55 mmol) and 2-[2-(2-oxo-1-piperazinyl)ethyl]-1H-isoindole-1,3(2H)-dione (150 mg, 0.55 mmol) in EtOH (2 mL) were stirred at 85° C. After 12 h, the solution was concentrated and the residue purified via column chromatography (silica, 0-8% MeOH in DCM (1% NH4OH)) yielding the title compound (100 mg, 42%) as a light yellow solid: LCMS (ES) m/e 432 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759340B2
Source datasetuspto-grants-2010_07
ORD IDord-a59c4c7876e24c65993fb6d2d9e21404
Source noteuspto-grants-2010_07