Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Pyridine methylene chloride | HCID 21875418 | — |
| Reactant | HCID 22386590 | HCID 22386590 | — |
| Product | HCID 22386582 | HCID 22386582 | 45.4% |
Reaction Steps
To a stirred solution of 4-amino-5-(4-methoxyphenoxy)quinazoline (1.0 g, 3.7 mmol) in 30 ml of dichloromethane pyridine (0.3 g, 3.7 mmol) and acetic anhydride (0.38 g, 3.7 mmol) were added at room temperature and stirring continued for 4 days. After evaporation under reduced pressure, 30 ml of 2-propanol was added and after cooling to 4° C. the solid was collected by filtration, washed, recrystallized from ethanol, filtrated again and dried at 50° C. in vacuo. to give 4-acetamido-5-(4methoxyphenoxy)quinazoline (0.5 g, 45.4%, m.p. 174-175° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06248771B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-a6389ff7668742f192eb69b5ce4e379d |
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| Source note | uspto-grants-2001_06 |
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