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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032695Generated: October 31, 2026

4-Benzylpiperazine-1-carboxamidine hemisulfate → HCID 178471120, compound

https://huagongshe.com/reaction/1032695

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Benzylpiperazine-1-carboxamidine hemisulfateHCID 2756652—
ReactantEthyl 2-formyl-3-methylsuccinateHCID 22164846—
ReactantHCID 178418922HCID 178418922—
ProductHCID 178471120HCID 17847112023%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04959368
Source datasetuspto-grants-1990_09
ORD IDord-4b85eb89b24b45459510d1a69a365f00
Source noteuspto-grants-1990_09