HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 9823946, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-(3-Bromopropoxy)-4-chlorobenzene | HCID 223534 | — |
| Reactant | 1,3-Dimethyl-6-(piperazin-1-yl)pyrimidine-2,4(1H,3H)-dione | HCID 12816873 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 9823946 | HCID 9823946 | 86.1% |
Reaction Steps
3 ml of triethylamine was added to 10 ml of an ethanol solution containing 2.5 g of 3-(4-chlorophenoxy)propyl bromide and 1.3 g of 1,3-dimethyl-6-(1-piperazinyl)-2,4(1H,3H)-pyrimidinedione, and the solution was then heated under reflux for 3 hours. Afterward, the reaction solution was concentrated to dryness, and the resultant residue was dissolved in chloroform and then washed with water. The thus obtained chloroform solution was dried and then concentrated, and the residue was recrystallized from ethanol/hexane, thereby preparing 1.96 g (yield: 86%) of 6-[4-(3-[4-chlorophenoxy]propyl)piperazin-1-yl]-1,3-dimethyl-2,4(1H,3H)-pyrimidinedione.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05332739 |
| Source dataset | uspto-grants-1994_07 |
| ORD ID | ord-e3b52a76561d41cd97afe2cec71b36c4 |
| Source note | uspto-grants-1994_07 |