Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Chloropropiophenone | HCID 70295 | — |
| Reactant | 1,3-Dimethyl-6-(piperazin-1-yl)pyrimidine-2,4(1H,3H)-dione | HCID 12816873 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 19011930 | HCID 19011930 | 65.9% |
Reaction Steps
In 15 ml of dioxane were dissolved 1.68 g of 3-chloropropiophenone, 2.24 g of 1,3-dimethyl-6-(1-piperazinyl)-2,4(1H,3H)-pyrimidinedione and 1.6 ml of triethylamine, and the solution was then stirred at 80° C. for 1 hour. Next, the solvent was distilled off, and the resultant residue was dissolved in chloroform, washed with water, and then concentrated to dryness. The residue was further recrystallized from methanol, thereby obtaining 2.58 g of the crystals of 1,3-dimethyl-6-[4-(3-oxo-3-phenylpropyl)piperazin-1-yl]-2,4(1H,3H)-pyrimidinedione.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05332739 |
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| Source dataset | uspto-grants-1994_07 |
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| ORD ID | ord-fa645afdbb414440a2eebefa3c6c12b2 |
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| Source note | uspto-grants-1994_07 |
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