Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032697Generated: October 30, 2026

4-Benzylpiperazine-1-carboxamidine hemisulfate → HCID 178520340, compound

https://huagongshe.com/reaction/1032697

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Benzylpiperazine-1-carboxamidine hemisulfateHCID 2756652—
ReactantHCID 66988753HCID 66988753—
SolventEthanolHCID 702—
ProductHCID 178520340HCID 17852034029%

Reaction Steps

10.0 g (73.5 mmoles) of 2-hydroxymethylenebutyrolactone sodium salt [synthesized by the method described in J. O. Fissekis et al., J. Org., Chem. 29, 2670 (1964)] and 19.6 g (73.3 mmoles) of 1-amidino-4-benzylpiperazine sulfate were added to 360 ml of ethanol, and the solution was refluxed for 5 hours. Ethanol was evaporated, and the residue was mixed with water and extracted with chloroform. The chloroform layer was dried, concentrated, and purified by silica gel column chromatography to give 6.66 g (yield 29%) of 2-(4-benzylpiperazino)-4-hydroxy-5-(2-hydroxyethyl)pyrimidine as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04959368
Source datasetuspto-grants-1990_09
ORD IDord-dd64aadefc88404db465c46502ead374
Source noteuspto-grants-1990_09