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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 48294Generated: October 29, 2026

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

https://huagongshe.com/reaction/48294

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 numberUS06703402B2
Source datasetuspto-grants-2004_03
ORD IDord-5db50b5ea4ea43ef9cb7d9dfaf0d16a5
Source noteuspto-grants-2004_03