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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1271274Erstellt: 26. Oktober 2026

Potassium Hydroxide → Tert-butyl 2-(4-((5,6-diphenylpyrazin-2-yl)(isopropyl)amino)butoxy)acetate

https://huagongshe.com/reaction/1271274

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium HydroxideHCID 14797—
Edukttert-Butyl bromoacetateHCID 79177—
Edukt4-((5,6-Diphenyl-Pyrazin-2-yl)(isopropyl)amino)butan-1-olHCID 18452655—
KatalysatorTetrabutylammonium hydrogen sulfateHCID 94433—
LösungsmittelBenzeneHCID 241—
ProduktTert-butyl 2-(4-((5,6-diphenylpyrazin-2-yl)(isopropyl)amino)butoxy)acetateHCID 6935719682,9%

Reaktionsschritte

22.84 g of 4-[N-(5,6-diphenylpyrazin-2-yl)-N-isopropylamino]-1-butanol was dissolved in 160 ml of benzene and 10.73 g of tetra-n-butylammonium hydrogen sulfate and 160 ml of an aqueous 40% potassium hydroxide solution were added. While stirring vigorously under ice cooling, 10.73 g of tert-butyl bromoacetate was added dropwise so as to control the inner temperature within a range from 5 to 10° C. After stirring for 45 minutes, an ice bath was removed and the mixture was stirred at room temperature for one hour. The reaction solution was diluted with water and then extracted with diethyl ether. The extract was washed with water and dried over anhydrous magnesium sulfate, and then the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography to obtain 21.70 g of the desired compound as a pale yellow oily substance.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07205302B2
Quelldatensatzuspto-grants-2007_04
ORD IDord-4113e19954ae4a85946d395a8cc38d07
Quellennotizuspto-grants-2007_04