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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079249Generated: October 30, 2026

Triethylamine → 6-fluoro-2-(2-methoxyphenyl)-3H-quinazolin-4-one

https://huagongshe.com/reaction/2079249

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Methoxybenzoyl chlorideHCID 88969—
Reactant2-Amino-5-fluorobenzamideHCID 10241003—
SolventTetrahydrofuranHCID 8028—
Product6-fluoro-2-(2-methoxyphenyl)-3H-quinazolin-4-oneHCID 13612147780.2%

Reaction Steps

o-Anisoyl chloride (15.7 g, 92 mmol) was added dropwise to a solution of 2-amino-5-fluorobenzamide (13.0 g, 84 mmol) and triethylamine (16 mL, 110 mmol) in tetrahydrofuran (100 mL) cooled in an ice bath. Immediately a precipitate started forming. Stirring of the solution was continued for 5 hours at room temperature. The formed precipitate was collected by filtration and was washed twice with diethyl ether and dried at 50° C. in vacuo. The dried solid was suspended in 2 N aqueous sodium hydroxide solution (250 mL) and heated at reflux until a clear solution was obtained (3 hours). The reaction mixture was cooled to room temperature and filtered. The filtrate was acidified to pH<1 with concentrated aqueous HCl. The formed precipitate was collected by filtration and washed twice with water, twice with methanol, and twice with diethyl ether. The solid was dried in an oven at 45° C. to yield 6-fluoro-2-(2-methoxyphenyl)-3H-quinazolin-4-one (18.2 g, 80%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928107B2
Source datasetuspto-grants-2011_04
ORD IDord-aa7d21db4220455c90533a01e6b2e29b
Source noteuspto-grants-2011_04