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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788043Generated: October 28, 2026

Water → 4-(3-chlorophenyl)-6-(4-fluorobenzoyl)-2(1H)-quinazolinone

https://huagongshe.com/reaction/1788043

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAmmonium AcetateHCID 517165—
Reactant2,2,2-trichloro-N-[2-(3-chlorobenzoyl)-4-(4-fluorobenzoyl)phenyl]-acetamideHCID 68688854—
SolventDimethyl SulfoxideHCID 679—
Product4-(3-chlorophenyl)-6-(4-fluorobenzoyl)-2(1H)-quinazolinoneHCID 6869075172.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

Acetic acid, ammonium salt (0.135 mol) was added at room temperature to a mixture of intermediate 4 (0.0675 mol) in DMSO (300 ml). The mixture was stirred at 60° C. for 4 hours, then brought to room temperature and poured out into water. The precipitate was filtered, washed with water, taken up in warm CH3CN, filtered, washed again with CH3CN, then with diethyl ether and dried under a vacuo, yielding 18.5 g (72%) of intermediate 5. The mother layer was purified by column chromatography over silica gel (15-40 μm) (eluent: DCM/MeOH:NH4OH 95/5/0.1). The pure fractions were collected and the solvent was evaporated. The residue was crystallized from 2-propanone/diethyl ether. The precipitate was filtered off and dried, yielding 1.8 g (7%) of 4-(3-chlorophenyl)-6-(4-fluorobenzoyl)-2(1H)-quinazolinone (intermediate 5), mp. 226° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07511138B2
Source datasetuspto-grants-2009_03
ORD IDord-4053017f320e42749ffe11e63cb6b74b
Source noteuspto-grants-2009_03