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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 7-Hydroxy-6-methoxy-4-phenoxyquinazoline | HCID 135496137 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7-(2-Bromoethoxy)-6-methoxy4-phenoxyquinazoline | HCID 21260311 | 63% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06184225B2 |
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| Source dataset | uspto-grants-2001_02 |
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| ORD ID | ord-94cb4230daf0477eb055c21707096ad9 |
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| Source note | uspto-grants-2001_02 |
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