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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473439Generated: October 29, 2026

Water → 2-(1-(2-(2-(Methylsulfonyl)phenyl)-1,5-naphthyridin-3-yl)ethyl)isoindoline-1,3-dione

https://huagongshe.com/reaction/473439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPhthalimideHCID 6809—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
ReactantHCID 58318628HCID 58318628—
SolventTetrahydrofuranHCID 8028—
Product2-(1-(2-(2-(Methylsulfonyl)phenyl)-1,5-naphthyridin-3-yl)ethyl)isoindoline-1,3-dioneHCID 58318636—

Reaction Steps

To a mixture of crude of 1-(2-(2-(methylsulfonyl)phenyl)-1,5-naphthyridin-3-yl)ethanol (700 mg, 2.13 mmol) and phthalimide (627 mg, 4.26 mmol) in THF (21 mL) was added triphenylphosphene (1.12 g, 4.26 mmol) at 0° C. The reaction mixture was stirred for 10 min at same temperature. Diisopropyl azodicarboxylate (0.9 mL, 4.26 mmol) was added to mixture at 0° C. The reaction mixture was stirred for overnight at 0° C. Water was added to reaction mixture and extracted with EtOAc. The organic layer was dried over Na2SO4 and concentrated in vacuo to give 2-(1-(2-(2-(methylsulfonyl)phenyl)-1,5-naphthyridin-3-yl)ethyl)isoindoline-1,3-dione: LC-MS (ESI) m/z 458.1 [M+H]+. It was carried on crude for next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633313B2
Source datasetuspto-grants-2014_01
ORD IDord-8dd5528d39a948789fea9a04b00fa25d
Source noteuspto-grants-2014_01