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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397778Generated: November 2, 2026

Dimethylformamide → Phthalimide

https://huagongshe.com/reaction/1397778

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPhthalimide potassium saltHCID 24194345—
Reactant2-(Bromomethyl)-5-chloro-3-(3-fluorophenyl)quinoxalineHCID 57707850—
ProductPhthalimideHCID 6809—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a heterogeneous mixture of 2-(bromomethyl)-5-chloro-3-(3-fluorophenyl)-quinoxaline (0.2401 g, 0.6829 mmol) in DMF (5.003 mL, 0.6829 mmol) was added potassium phthalimide (0.3162 g, 1.707 mmol) and the heterogeneous mixture was stirred at 100° C. After stirring at 100° C. for 1 h, the mixture was concentrated under reduced pressure and triturated with water (30 mL). The precipitate was collected by filtration. The solid was washed with water (50 mL), then MeOH (100 mL), and dried to give 24(5-chloro-3-(3-fluorophenyl)-quinoxalin-2-yl)methyl)isoindoline-1,3-dione as an off-white solid: 1H NMR (400 MHz, DMSO-d6) δ ppm 8.04 (1 H, dd, J=7.6, 1.4 Hz), 7.84-7.92 (5 H, m), 7.60-7.81 (4 H, m), 7.38-7.46 (1 H, m), 5.22 (2 H, s); LC-MS (ESI) m/z 418.1 [M+H]+. The crude product was carried on crude without purification for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901135B2
Source datasetuspto-grants-2014_12
ORD IDord-577cef92dbb0469fa4e982ef6a93b5b7
Source noteuspto-grants-2014_12