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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661830Generated: October 25, 2026

Ethyl orthoformate → 4(3H)-Quinazolinone, 3-(3-bromo-2-methylphenyl)-2-methyl-

https://huagongshe.com/reaction/661830

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl orthoformateHCID 31214—
ReactantAcetanthranilHCID 68236—
Reactant3-Bromo-o-toluidineHCID 123538—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product4(3H)-Quinazolinone, 3-(3-bromo-2-methylphenyl)-2-methyl-HCID 6336920%

Reaction Steps

A solution of 2-methyl-4H-benzo[d][1,3]oxazin-4-one (300 mg, 1.862 mmol), 3-bromo-2-methylaniline (346 mg, 1.862 mmol), and triethoxymethane (276 mg, 1.862 mmol) in THF (2 mL) was heated overnight in a sealed tube at 100° C. The mixture was cooled to rt and diluted with DCM. The solution was washed with water and NaHCO3 (aq), and dried and concentrated. The residue was purified by column chromatography (eluting with a gradient from 90:10 to 50:50 hexane-EtOAc) and the crude product was triturated in hexane to give 3-(3-bromo-2-methylphenyl)-2-methylquinazolin-4(3H)-one as an off-white solid (120 mg, 20%). 1H NMR (400 MHz, chloroform-d) δ 8.28 (1H, dd, J=7.92, 1.10 Hz), 7.77-7.82 (1H, m), 7.68-7.73 (2H, m), 7.47-7.52 (1H, m), 7.22-7.25 (1H, m), 7.13-7.17 (1H, m), 2.20 (6H, s). Mass spectrum m/z 329, 331 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084620B2
Source datasetuspto-grants-2011_12
ORD IDord-9f08a6f7055a4093bfc79c289320315c
Source noteuspto-grants-2011_12