HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Phenylpiperazine → 6-Methyl-5-(4-phenyl-1-piperazinyl)-2,4(1H, 3H)-pyrimidinedione, hydrate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Phenylpiperazine | HCID 7096 | — |
| Reactant | 2,4(1H,3H)-Pyrimidinedione, 5-bromo-6-methyl- | HCID 84757 | — |
| Reactant | Potassium fluoride dihydrate | HCID 23708904 | — |
| Product | 6-Methyl-5-(4-phenyl-1-piperazinyl)-2,4(1H, 3H)-pyrimidinedione, hydrate | HCID 131714289 | — |
Reaction Steps
A mixture of 20.5 g (0.10 mole) of 5-bromo-6-methyl-2,4(1H, 3H)-pyrimidinedione and 10.3 g (0.11 mole) of potassium fluoride dihydrate in 150 ml of 1-phenylpiperazine was heated under reflux at 105° for 72 hours and cooled. The reaction mixture was poured into 200 ml of ice water. The solid was collected, washed with water, and recrystallized from methanol to give 7.12 g of the product as a white solid, mp>300° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04532240 |
| Source dataset | uspto-grants-1985_07 |
| ORD ID | ord-8ef45b1fe7da4a5ab02088c7701be9d0 |
| Source note | uspto-grants-1985_07 |