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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5722Generated: October 26, 2026

Sodium Chloride → 1-[N,O-Bis(5-Isoquinolinesulphonyl)Tyrosyl]-4-(3-Phenylpropyl)Piperazine

https://huagongshe.com/reaction/5722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant(3-Bromopropyl)benzeneHCID 12503—
Reactant1-[N,O-Bis(5-Isoquinolinesulfonyl)Tyrosyl]PiperazineHCID 54291950—
SolventDimethylformamideHCID 6228—
Product1-[N,O-Bis(5-Isoquinolinesulphonyl)Tyrosyl]-4-(3-Phenylpropyl)PiperazineHCID 5388462760.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

301 mg of the crude product obtained in Example 28 and 95 mg of 3-phenylpropyl bromide were dissolved in 5 ml of dimethylformamide, and to the solution were added 66 mg of potassium carbonate and 72 mg of sodium iodide. After stirring at 80° C. for 7 hours, 30 ml of saturated sodium chloride was added to the reaction mixture, which was then extracted with 40 ml of ethyl acetate, and the extract was washed with 30 ml of saturated sodium chloride aqueous solution, dried over magnesium sulfate, and concentrated under a reduced pressure. The resulting residue was applied to a silica gel column and eluted with chloroform/methanol (40:1) to obtain 216 mg of the title compound in a yellow amorphous form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05245034
Source datasetuspto-grants-1993_09
ORD IDord-0c3b815bf40646aca5a9b9a17bb5ca53
Source noteuspto-grants-1993_09