HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N-(6-aminopyrimidin-4-yl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Pyrimidine-4,6-diamine | HCID 79608 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N-(6-aminopyrimidin-4-yl)acetamide | HCID 3031498 | 61% |
Reaction Steps
To a stirred suspension of pyrimidine-4,6-diamine (500 mg, 4.55 mmol) in dioxane (20 mL) was added acetic anhydride (465 mg, 4.55 mmol) and the resulting mixture was heated under reflux for 15 hours. The reaction was cooled to room temperature and the resulting precipitate was collected by filtration. The filtercake was dissolved in 1N HCl and the pH of the aqueous phase adjusted to 7 by the addition of 1N NaOH. The resulting white precipitate was collected by filtration and dried to afford the desired product as a white solid (420 mg, 61% yield). LCMS (ESI) m/z: 152.0 [M+H+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08697708B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-df25aac569e74280ab2451790da6bd3b |
| Source note | uspto-grants-2014_04 |