HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Benzylpiperazine-1-carboxamidine hemisulfate → HCID 178471120, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Benzylpiperazine-1-carboxamidine hemisulfate | HCID 2756652 | — |
| Reactant | Ethyl 2-formyl-3-methylsuccinate | HCID 22164846 | — |
| Reactant | HCID 178418922 | HCID 178418922 | — |
| Product | HCID 178471120 | HCID 178471120 | 23% |
Reaction Steps
A solution of 2.16 g (10 mmoles) of ethyl 2-formyl-3-methylsuccinate [Zhur. Obshche i Khim., 30, 2250 (1960)] was added to a mixture of 2.67 g (10 mmoles) of 1-amidino-4-benzylpiperazine sulfate, 1.12 g (10 mmoles) of tert-C4H9OK and 12 ml of tert-C4O9OH. The mixture was then refluxed for 6 hours. The reaction mixture was cooled, and extracted by adding water and CHCl3. The CHCl3 layer was dried over anhydrous MgSO4, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (CH2Cl2 :CH3OH=95:5) to give 0.68 g (yield 23%) of 2-(4-benzylpiperazino)-5-(1-ethoxycarbonylethyl)-4-hydroxypyrimidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04959368 |
| Source dataset | uspto-grants-1990_09 |
| ORD ID | ord-4b85eb89b24b45459510d1a69a365f00 |
| Source note | uspto-grants-1990_09 |