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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274219Generated: October 26, 2026

Cerous carbonate → 2-Chloro-6-(3,5-dimethoxyphenyl)-7-methoxyquinazoline

https://huagongshe.com/reaction/2274219

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCerous carbonateHCID 160516—
Reactant(3,5-Dimethoxyphenyl)boronic acidHCID 4374257—
Reactant6-Bromo-2-chloro-7-methoxyquinazolineHCID 59199276—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Solvent1,4-DioxaneHCID 31275—
Product2-Chloro-6-(3,5-dimethoxyphenyl)-7-methoxyquinazolineHCID 8671359538%

Reaction Conditions

Temperature85 °C

Reaction Steps

A mixture of 6-bromo-2-chloro-7-methoxyquinazoline (2.4 g, 8.82 mmol), 3,5-dimethoxyphenylboronic acid (1.6 g, 8.82 mmol), cerium carbonate (8.6 g, 26.46 mmol) and Pd(PPh3)2Cl2 (1.4 g, 2.1 mmol) in THF (10 mL), dioxane (10 mL) and water (2 mL) was degassed with nitrogen three times and stirred at 85° C. for 3 h. LCMS monitored the reaction was completed. The mixture was cooled to RT and extracted with dichloromethane (3×50 mL). The organic layers were separated, combined, washed with water and brine, dried over sodium sulfate, filtered and concentrated. The residue was purified by silica gel chromatography (petroleum ether:ethyl acetate=1:4) to give the title compound (1.1 g, 38%) as a white solid. MS (ES+) C17H15ClN2O3 requires: 330, 332. Found: 331, 333 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126951B2
Source datasetuspto-grants-2015_09
ORD IDord-97b38dcdff9344a1a223271e3e9601a8
Source noteuspto-grants-2015_09