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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661832Generated: November 2, 2026

Ethyl orthoformate → HCID 59375009, compound

https://huagongshe.com/reaction/661832

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl orthoformateHCID 31214—
Reactant2-Amino-5-fluorobenzoic acidHCID 101412—
Reactant3-Bromo-o-toluidineHCID 123538—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 59375009HCID 5937500956%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 2-amino-5-fluorobenzoic acid (1.00 g, 6.45 mmol), 3-bromo-2-methylaniline (1.199 g, 6.45 mmol) and triethoxymethane (0.955 g, 6.45 mmol) in THF (2 mL) was heated at 110° C. overnight in a sealed tube. The mixture was cooled to rt and diluted with EtOAc. The solution was washed with NaHCO3 (aq) and water, then was dried and concentrated. The residue was purified by column chromatography (eluting with a gradient from 80:20 to 70:30 hexane-EtOAc) to give 3-(3-bromo-2-methylphenyl)-6-fluoroquinazolin-4(3H)-one as a white solid (1.2 g, 56%). 1H NMR (400 MHz, chloroform-d) δ 8.00 (1H, dd, J=8.4, 3.1 Hz), 7.93 (1H, s), 7.81 (1H, dd, J=9.0, 4.8 Hz), 7.74 (1H, dd, J=6.9, 2.3 Hz), 7.50-7.58 (1H, m), 7.21-7.26 (2H, m), 2.25 (3H, s). Mass spectrum m/z 333, 335 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084620B2
Source datasetuspto-grants-2011_12
ORD IDord-8dbc0b21b3f54bee80fb0cb52c2d91bf
Source noteuspto-grants-2011_12