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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 634702Generated: October 30, 2026

1,2-Dibromoethane → 7-(2-Bromoethoxy)-6-methoxy4-phenoxyquinazoline

https://huagongshe.com/reaction/634702

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DibromoethaneHCID 7839—
ReactantPotassium CarbonateHCID 11430—
Reactant7-Hydroxy-6-methoxy-4-phenoxyquinazolineHCID 135496137—
SolventDimethylformamideHCID 6228—
Product7-(2-Bromoethoxy)-6-methoxy4-phenoxyquinazolineHCID 2126031163%

Reaction Conditions

Temperature85 °C

Reaction Steps

1,2-Dibromoethane (1.6 ml, 18.6 mmol) was added to 7-hydroxy-6-methoxy-4-phenoxyquinazoline (0.5 g, 1.86 mmol), (prepared as described for the starting material in Example 16), and potassium carbonate (1.2 g, 8.7 mmol) in DMF (60 ml) and the mixture was heated at 85° C. for 2 hours, and was then allowed to cool. The insolubles were removed by filtration, and the volatiles were removed from the filtrate by evaporation to give a residue which was purified by column chromatography eluting with methylene chloride/methanol (97/3) to give 7-(2-bromoethoxy)-6-methoxy-4-phenoxyquinazoline (440 mg, 63%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06184225B2
Source datasetuspto-grants-2001_02
ORD IDord-94cb4230daf0477eb055c21707096ad9
Source noteuspto-grants-2001_02