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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651056Generated: October 25, 2026

1H-Isoindole-1,3(2H)-dione, 2-(2-bromoethyl)- → (S)-N-(alpha-ethylbenzyl)-2-phenyl-3-(2-phthalimidoethoxy)quinoline-4-carboxamide

https://huagongshe.com/reaction/651056

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Isoindole-1,3(2H)-dione, 2-(2-bromoethyl)-HCID 11325—
ReactantPotassium CarbonateHCID 11430—
ReactantTalnetantHCID 5311424—
SolventTetrahydrofuranHCID 8028—
Product(S)-N-(alpha-ethylbenzyl)-2-phenyl-3-(2-phthalimidoethoxy)quinoline-4-carboxamideHCID 11800901—

Reaction Steps

1.90 g (5.0 mmol) of (S)-N-(α-ethylbenzyl)-3-hydroxy-2-phenylquinoline-4-carboxamide (product of Description 1) were dissolved in 20 ml of THF. 3.80 g (14.9 mmol) of N-(2-bromoethyl)phthalimide dissolved in 15 ml of THF, 2.00 g (14.5 mmol) of K2CO3 and 0.25 g of KI were added and the suspension was stirred at room temperature for 2.5 hours and then refluxed for 2 hours. Additional 1.90 g (7.4 mmol) of N-(2-bromoethyl)phthalimide and a catalytic amount of KI were added and the reaction refluxed for 3.5 hours; additional 0.50 g (2.0 mmol) of N-(2-bromoethyl)phthalimide and a catalytic amount of KI were added and the reaction refluxed for 5 hours.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06277862B1
Source datasetuspto-grants-2001_08
ORD IDord-02f654b91404405688046646914f2fab
Source noteuspto-grants-2001_08