HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032699Generated: November 2, 2026
Potassium Hydroxide → HCID 178470707, compound
https://huagongshe.com/reaction/1032699
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Butanedioic acid, 2-acetyl-, 1,4-diethyl ester | HCID 66197 | — |
| Reactant | 4-Benzylpiperazine-1-carboxamidine hemisulfate | HCID 2756652 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178470707 | HCID 178470707 | 17.6% |
Reaction Steps
Potassium hydroxide (3.1 g) was added to 200 ml of ethanol, and the mixture was stirred for 30 minutes. Then, 12.4 g of 1-amidino-4-benzylpiperazine sulfate was added. The mixture was stirred at room temperature for 10 minutes. To the solution was added 12.4 g of diethyl acetylsuccinate. The mixture was refluxed for 2 hours. Then, 200 ml of toluene was added, and the mixture was refluxed for 3 hours. After the reaction, ethanol was evaporated, and the residue was poured into 50 ml of an aqueous solution of hydrochloric acid. NaHCO3 was added to the solution to neutralize it. The precipitated solid was washed with water and dried over P2O5 to give 2.55 g (yield 15%) of 2-(4-benzylpiperazino)-5-ethoxycarbonylmethyl-4-hydroxy-6-methylpyrimidine as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04959368 |
|---|
| Source dataset | uspto-grants-1990_09 |
|---|
| ORD ID | ord-6eeed99592f143d0b3ed66f071cf2705 |
|---|
| Source note | uspto-grants-1990_09 |
|---|