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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989348Generated: October 29, 2026

2-(Dimethylamino)ethanol → 4-(2,4-Dichloroanilino)-7-[2-(dimethylamino)ethoxy]benzo[g]quinoline-3-carbonitrile

https://huagongshe.com/reaction/989348

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Dimethylamino)ethanolHCID 7902—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant4-(2,4-Dichloroanilino)-7-hydroxybenzo[g]quinoline-3-carbonitrileHCID 21956480—
SolventDichloromethaneHCID 6344—
Product4-(2,4-Dichloroanilino)-7-[2-(dimethylamino)ethoxy]benzo[g]quinoline-3-carbonitrileHCID 2195645820.5%

Reaction Steps

To a suspension of 189.1 mg (0.50 mmol) of 4-(2,4-dichloroanilino)-7-hydroxybenzo[g]quinoline-3-carbonitrile, 207.2 mg (0.79mmol) of triphenylphosphine and 66.9 mg (0.75 mmol) of 2-(dimethylamino)-ethanol in 3.0 mL of anhydrous methylene chloride at 0° C. is added dropwise diethyl azodicarboxylate. The resulting reaction mixture is stirred at room temperature under nitrogen for 2 days. The solvent is concentrated in vacuo and the residue is purified on preparative thin layer chromatography (developing solvent: 9:1 methylene chloride/methanol) to provide 46.3 mg (20.5%) of 4-(2,4-dichloroanilino)-7-[2-(dimethylamino)ethoxy]benzo[g]quinoline-3-carbonitrile as a yellow solid, mp 115-117° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06638929B2
Source datasetuspto-grants-2003_10
ORD IDord-15a2f0092d9d42419a578f7faeccbfef
Source noteuspto-grants-2003_10