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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 841776Generated: October 25, 2026

Diisopropylethylamine → 7-[2-(5-Trifluoromethyl-pyridin-2-yl)-benzoylamino]-quinoline-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/841776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantEthyl 7-aminoquinoline-3-carboxylateHCID 9877801—
Reactant2-(5-(Trifluoromethyl)pyridin-2-yl)benzoic acidHCID 22736909—
Solvent1,2-DichloroethaneHCID 11—
SolventThionyl ChlorideHCID 24386—
Product7-[2-(5-Trifluoromethyl-pyridin-2-yl)-benzoylamino]-quinoline-3-carboxylic acid ethyl esterHCID 6989134585%

Reaction Steps

2-(5-Trifluoromethyl-pyridin-2-yl)-benzoic acid (325 mg, 1.05 mmol) was dissolved in 15 ml of thionyl chloride, and the mixture heated at 60 C. After 4 h, the volatiles were removed under vacuum, the residue combined with 7-amino-quinoline-3-carboxylic acid ethyl ester (100 mg, 0.46 mmol), dissolved in 1,2-dichloroethane (15 ml), and diisopropylethylamine (300 mg, 2.31 mmol) added. After heating at reflux for 48 h, the reaction mixture was washed with 1N HCl, dried (magnesium sulfate), filtered, and concentrated under vacuum. The resulting residue was purified by silica gel chromatography eluting with 50% ethyl acetate in hexanes to provide 180 mg (85%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06369075B1
Source datasetuspto-grants-2002_04
ORD IDord-c2a6f9c07db64467a438da7fa0104db3
Source noteuspto-grants-2002_04