Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Aminopyrimidine | HCID 7978 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,4,5-Trichloropyrimidine | HCID 237259 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 59586803 | HCID 59586803 | — |
Reaction Steps
The mixture of pyrimidin-2-amine (48 mg, 0.50 mmol), 2,4,5-trichloropyrimidine (57 μL, 0.5 mmol), and potassium carbonate (69 mg, 0.5 mmol) in 3 mL of 1,4-dioxane is heated at 110° C. over night. The precipitate is filtered, washed by cold EtOH, and dried in vacuo to afford N-(2,5-Dichloropyrimidin-4-yl)pyrimidin-2-amine; ESMS m/z 242.0 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08440681B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-e70772a26ad84bf5a3bf400f91dc28df |
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| Source note | uspto-grants-2013_05 |
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