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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441461Generated: November 3, 2026

Ammonium Acetate → 4-(3-chlorophenyl)-6-(4-methoxybenzoyl)-2(1H)-quinazolinone

https://huagongshe.com/reaction/1441461

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium AcetateHCID 517165—
Reactant2,2,2-trichloro-N-[2-(3-chlorobenzoyl)-4-(4-methoxybenzoyl)phenyl]-acetamideHCID 17976099—
SolventDimethyl SulfoxideHCID 679—
Product4-(3-chlorophenyl)-6-(4-methoxybenzoyl)-2(1H)-quinazolinoneHCID 6868945977.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

Acetic acid, ammonium salt (0.107 mol) was added at room temperature to a mixture of intermediate 12 (0.0536 mol) in DMSO (250 ml). The mixture was stirred at 60° C. for 4 hours then brought to room temperature, poured out into ice water and stirred. The precipitate was filtered, washed with water and taken up in warm CH3CN. The precipitate was filtered, washed with diethyl ether and dried under a vacuo, yielding 16.2 g (77%) of intermediate 13. The mother layer was evaporated. The residue 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 (1.2 g, 6%) was crystallized from 2-propanone. The precipitate was filtered off and dried, yielding 0.9 g (4%) of 4—(3-chlorophenyl)-6-(4-methoxybenzoyl)-2(1H)quinazolinone (intermediate 13), mp. 248° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07655654B2
Source datasetuspto-grants-2010_02
ORD IDord-458b67b9b60a4232ab6bc1342d0e4a4e
Source noteuspto-grants-2010_02