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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033161Generated: October 31, 2026

Triethylamine → 3-(6-Fluoroquinolin-2-on-7-yl)-1-methyl-6-trifluoromethyluracil

https://huagongshe.com/reaction/1033161

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-(3-Chloro-6-fluoro-3,4-dihydroquinolin-2-on-7-yl)-1-methyl-6-trifluoromethyluracilHCID 19025383—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product3-(6-Fluoroquinolin-2-on-7-yl)-1-methyl-6-trifluoromethyluracilHCID 1902538597.4%

Reaction Steps

A stirred solution of 5.2 grams (0.013 mole) of 3-(3-chloro-6-fluoro-3,4-dihydroquinolin-2-on-7-yl)-1-methyl-6-trifluoromethyluracil and 6.2 grams (0.061 mole) of triethylamine in 200 mL of tetrahydrofuran was concentrated under reduced pressure to a residue. The residue was dissolved in methylene chloride and washed with water. The organic layer was dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure, yielding 4.5 grams of 3-(6-fluoroquinolin-2-on-7-yl)-1-methyl-6-trifluoromethyluracil, mp 179° C., dec. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05310723
Source datasetuspto-grants-1994_05
ORD IDord-111766c06f1c49099b4d4be7a08e703c
Source noteuspto-grants-1994_05