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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168826Generated: November 2, 2026

Triethylamine → N-[4-hydroxy-7-(trifluoromethyl)quinolin-3-yl]butanamide

https://huagongshe.com/reaction/1168826

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantButyryl chlorideHCID 8855—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178479096HCID 178479096—
SolventTetrahydrofuranHCID 8028—
ProductN-[4-hydroxy-7-(trifluoromethyl)quinolin-3-yl]butanamideHCID 17845447583.8%

Reaction Steps

Butyryl chloride (1.5 mL, 14.5 mmol) was added dropwise to a mixture of 3-amino-7-(trifluoromethyl)-4-quinolinol hydrochloride (3.5 g, 13.2 mmol), triethylamine (6.1 mL, 43.6 mmol) and anhydrous tetrahydrofuran (30 mL). The reaction mixture was allowed to stir for 16 hours. A small amount of aqueous sodium bicarbonate was added and the reaction mixture was stirred for 0.5 hours. The tetrahydrofuran was removed under vacuum. The resulting solid was stirred with diethyl ether, isolated by filtration, washed with water and diethyl ether, and then dried in a vacuum oven at 80° C. overnight to provide 3.3 g of N-[4-hydroxy-7-(trifluoromethyl)quinolin-3-yl]butanamide as a cream colored solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06627640B2
Source datasetuspto-grants-2003_09
ORD IDord-285f3e11d4d2415e81c50055e7b631d1
Source noteuspto-grants-2003_09