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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 973767Erstellt: 23. Oktober 2026

phenylalaninol, (S)- → (S)-beta-[(1-phenyl-6-chloro-1H-pyrazolo[3,4-d]pyrimidin-4-yl)amino]benzenepropanol

https://huagongshe.com/de/reaction/973767

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktphenylalaninol, (S)-HCID 447213—
Edukt4,6-dichloro-1-phenyl-1H-pyrazolo[3,4-d]pyrimidineHCID 4737109—
LösungsmittelEthanolHCID 702—
Produkt(S)-beta-[(1-phenyl-6-chloro-1H-pyrazolo[3,4-d]pyrimidin-4-yl)amino]benzenepropanolHCID 1566712597%

Reaktionsschritte

2.5 g of the starting material 1-phenyl-4,6-dichloropyrazolo[3,4-d]pyrimidine was suspended in 60 ml of ethanol. Next, 4.28 g of (S)-(-)-2-amino-3-phenyl-1-propanol was added and the reaction was allowed to stir for 24 hours. The solvent was then removed under vacuum and the crude oil was purified by flash chromatography (10-15-20% isopropyl alcohol/hexane) to yield 3.5 g of (S)-β-[(1-phenyl-6-chloro-1H-pyrazolo[3,4-d]pyrimidin-4-yl)amino]benzenepropanol (97%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05064947
Quelldatensatzuspto-grants-1991_11
ORD IDord-86082389e41941b6925f0e2b852e457e
Quellennotizuspto-grants-1991_11