HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228684Generated: October 30, 2026
1-(2-Hydroxy-5-methoxyphenyl)ethan-1-one → HCID 57756486, compound
https://huagongshe.com/reaction/228684
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-(2-Hydroxy-5-methoxyphenyl)ethan-1-one | HCID 69714 | — |
| Reactant | 4-Chloro-6,7-dimethoxyquinazoline | HCID 2769364 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | 1,2-Dichlorobenzene | HCID 7239 | — |
| Product | HCID 57756486 | HCID 57756486 | 50% |
Reaction Steps
4-Chloro-6,7-dimethoxyquinazoline (59 mg), 2-hydroxy-5-methoxyacetophenone (213 mg), and 4-dimethylaminopyridine (173 mg) were suspended in o-dichlorobenzene (5 ml), and the suspension was stirred at 160° C. for 10 min. The reaction solution was cooled to room temperature, the solvent was then removed therefrom by distillation under the reduced pressure, and chloroform was added to the residue. The mixture was washed with a 1 N aqueous potassium hydroxide solution and saturated brine and was dried over anhydrous magnesium sulfate. The solvent was removed therefrom by distillation under the reduced pressure, and the residue was purified by column chromatography using chloroform and by thin layer chromatography using acetone-hexane to give the title compound (46.5 mg, yield 50%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07560558B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-d81b756157d94d8e8ad3c0fc7edeab92 |
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| Source note | uspto-grants-2009_07 |
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