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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 624532Generated: October 27, 2026

Urea → 2,7-Dichloro-6-fluoroquinazoline

https://huagongshe.com/reaction/624532

Reaction equation

Participants

RoleNameHCIDCharge
ReactantUreaHCID 1176—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant2-Amino-4-chloro-5-fluorobenzaldehydeHCID 85705870—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product2,7-Dichloro-6-fluoroquinazolineHCID 8670540812.3%

Reaction Conditions

Temperature180 °C

Reaction Steps

A mixture of 2-amino-4-chloro-5-fluorobenzaldehyde (0.30 g, 1.73 mmol) and urea (1.04 g, 17.3 mmol) was heated to 180° C. for 1 h, then cooled to RT. The solid was then suspended in a mixture of EtOAc and water and then it was filtered and the collected solid was washed with water several times, then air-dried. This intermediate quinazolinone was then suspended in phosphorus oxychloride (3.0 mL, 32.2 mmol) and then heated to 100° C. for 1 h. After cooling to RT, the mixture was added dropwise to an ice-water mixture. The mixture was stirred for 5 minutes and then the product was extracted into EtOAc (3×). The combined extracts were dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo to give an oil that was purified by silica gel chromatography to give 2,7-dichloro-6-fluoroquinazoline as a white solid (46 mg, 12% yield). m/z=217 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09303028B2
Source datasetuspto-grants-2016_04
ORD IDord-b2872013beb34d868a81ac5df0441d31
Source noteuspto-grants-2016_04