HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371471Generated: October 25, 2026
Potassium Carbonate → 5-[4-(4-cyanophenyl)-1-piperazinyl]-6-methyl-2,4-(1H,3H)-pyrimidinedione
https://huagongshe.com/reaction/371471
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,4(1H,3H)-Pyrimidinedione, 5-bromo-6-methyl- | HCID 84757 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | 4-(Piperazin-1-yl)benzonitrile | HCID 2733995 | — |
| Solvent | Hexamethylphosphoramide | HCID 12679 | — |
| Product | 5-[4-(4-cyanophenyl)-1-piperazinyl]-6-methyl-2,4-(1H,3H)-pyrimidinedione | HCID 20272865 | 29.9% |
Reaction Steps
A mixture of 20.5 g (0.10 mole) of 5-bromo-6-methyl-2,4(1H,3H)-pyrimidinedione, 18.1 g (0.10 mole) of 4-(4-cyanophenyl)piperazine, 6.4 g (0.11 mole) of anhydrous potassium fluoride, 15.2 g (0.1 mole) of powdered potassium carbonate in 100 ml of hexamethyl phosphoramide was heated at 140° C. for 24 hours. The mixture was cooled and poured into 500 ml of ice water. The solid was collected and washed with 100 ml of water. Recrystallization from N,N-dimethylformamide and drying in vacuo at 78° C. for 16 hours gave 9.3 g of the product as a dull solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04532240 |
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| Source dataset | uspto-grants-1985_07 |
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| ORD ID | ord-5fd490a8d73246e0a4b4afa32a29c68a |
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| Source note | uspto-grants-1985_07 |
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