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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 275009Erstellt: 26. Oktober 2026

2-Amino-1-phenylpropan-1-ol hydrochloride → alpha-[1-[(1-phenyl-6-chloro-1H-pyrazolo[3,4-d]pyrimidin-4-yl)amino]ethyl]benzenemethanol

https://huagongshe.com/reaction/275009

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Amino-1-phenylpropan-1-ol hydrochlorideHCID 9065—
EduktPotassium HydroxideHCID 14797—
Edukt4,6-dichloro-1-phenyl-1H-pyrazolo[3,4-d]pyrimidineHCID 4737109—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
Produktalpha-[1-[(1-phenyl-6-chloro-1H-pyrazolo[3,4-d]pyrimidin-4-yl)amino]ethyl]benzenemethanolHCID 5384115790%

Reaktionsschritte

390 mg of 1-phenyl-4,6-dichloropyrazolo[3,4-d]pyrimidine was suspended in 15 ml 95% ethanol. 828 mg norephedrine HCl was dissolved in 100 ml H2O, made basic with 10% KOH, and the free base extracted with 100 ml ether. The organic was dried over MgSO4, filtered, and concentrated to yield an oil which was added to the stirred reaction. After 4 hours the solution became clear and the solvent was removed under vacuum. The crude oil was then purified by radial chromatography (5-10-20% isopropyl alcohol/hexane, 4 mm plate) to yield 535 mg of [R-(S*,R*)]-α-[1-[(1-phenyl-6-chloro-1H-pyrazolo[3,4-d]pyrimidin-4-yl) amino]ethyl]benzenemethanol (90%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05391739
Quelldatensatzuspto-grants-1995_02
ORD IDord-b8efe1e099404e899f765374d95c304e
Quellennotizuspto-grants-1995_02