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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 523219Generated: October 29, 2026

Methyl iodide → 3-(3-Bromo-2-methylphenyl)-8-methoxy-1-methylquinazoline-2,4-dione

https://huagongshe.com/reaction/523219

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantCesium carbonateHCID 10796—
Reactant3-(3-bromo-2-methylphenyl)-8-methoxyquinazoline-2,4(1H,3H)-dioneHCID 117760671—
SolventTetrahydrofuranHCID 8028—
Product3-(3-Bromo-2-methylphenyl)-8-methoxy-1-methylquinazoline-2,4-dioneHCID 11776120679.6%

Reaction Steps

A mixture of 3-(3-bromo-2-methylphenyl)-8-methoxyquinazoline-2,4(1H,3H)-dione (535 mg, 1.48 mmol), iodomethane (0.185 mL, 2.96 mmol) and Cs2CO3 (965 mg, 2.96 mmol) in THF (20 mL) was stirred at room temperature overnight. The mixture was filtered and concentrated. The residue was dissolved in DCM, washed sequentially with saturated aqueous NaHCO3 and water, dried and concentrated. The residue was purified by column chromatography on silica gel (40 g silica), eluting with EtOAc-hexanes (gradient from 0-100%), to give 3-(3-bromo-2-methylphenyl)-8-methoxy-1-methylquinazoline-2,4(1H,3H)-dione (442 mg). Mass spectrum m/z 375, 377 (M+H)+. 1H NMR (400 MHz, chloroform-d) δ 7.90 (dd, J=7.2, 2.3 Hz, 1H), 7.66 (dd, J=8.0, 1.2 Hz, 1H), 7.31-7.22 (m, 2H), 7.22-7.19 (m, 1H), 7.17-7.13 (m, 1H), 3.97 (s, 3H), 3.89 (s, 3H), 2.23 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334290B2
Source datasetuspto-grants-2016_05
ORD IDord-b0429b8a53fa4de380b40d88e53e87c8
Source noteuspto-grants-2016_05