HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Allylpiperazine → HCID 135804944, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Allylpiperazine | HCID 806422 | — |
| Reactant | 4(3H)-Quinazolinone, 2-(ethylthio)- | HCID 135435974 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 135804944 | HCID 135804944 | 89% |
Reaction Steps
N-allylpiperazine (37 g) was added to 30 g of 2-ethylthio-4(3H)-quinazolinone [J. Med. Chem., 11, 392 (1968)], and the mixture was stirred at 140° to 160° C. for 5 hours in a stream of nitrogen. After cooling, the reaction mixture was suspended in ethyl acetate and filtered. The resulting crude crystals were recrystallized from ethanol/ethyl acetate to give 35 g of 2-(4-allyl-l-piperazinyl)-4(3H)-quinazolinone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04877790 |
| Source dataset | uspto-grants-1989_10 |
| ORD ID | ord-27f8f9715306424588bc18569fe4914b |
| Source note | uspto-grants-1989_10 |