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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1801685Erstellt: 25. Oktober 2026

Ethanol → [1-(3,5-Dimethyl-phenyl)-1H-pyrazolo[3,4-d]pyrimidine-4-yl]-[2-(2-methoxy-ethoxy)-ethyl]-amine

https://huagongshe.com/reaction/1801685

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktDiisopropyl EtherHCID 7914—
Edukt2-(2-Methoxyethoxy)ethanamineHCID 520530—
Edukt4-chloro-1-(3,5-dimethylphenyl)-1H-pyrazolo[3,4-d]pyrimidineHCID 4962119—
LösungsmittelAcetonitrileHCID 6342—
Produkt[1-(3,5-Dimethyl-phenyl)-1H-pyrazolo[3,4-d]pyrimidine-4-yl]-[2-(2-methoxy-ethoxy)-ethyl]-amineHCID 4418250956,8%

Reaktionsbedingungen

Temperatur27.5 °C

Reaktionsschritte

60.0 ml of ethanol and 10.0 g (0.038 mol) of 4-chloro-1-(3,5-dimethyl-phenyl)-1H-pyrazolo[3,4-d]pyrimidine (Compound No. 79) were charged into a 250 ml of 4 necked round bottom flask connected to a mechanical stirrer, thermometer socket, condenser and addition funnel. 22.40 g (0.18 mol) of 2-(2-Methoxy-ethoxy)-ethyl amine was charged at 25-30° C. under stirring. Reaction mass temperature was raised to reflux. Maintained the mass temperature at reflux for 5 hours. Reaction mass temperature was cooled to 25-30° C. Maintained the mass temperature at 25-30° C. for 60 min. Reaction mass temperature cooled to 0-5° C. Maintained the mass temperature at 0-5° C. for 60 min. Solid does not formed. Distilled off Ethanol completely under vacuum. Crude oily mass was obtained. Oily mass was dissolved in 45 ml of acetonitrile. 300.0 ml of isopropyl ether was added. Solid was formed. Solid was filtered and solid was washed with 50.0 ml of isopropyl ether. Compound was dried under vacuum at 60-65° C. Dry weight of the compound: 7.50 g (yield—56.80%). Melting point: 90.4° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08349847B2
Quelldatensatzuspto-grants-2013_01
ORD IDord-cd83a7dbadbf4b988373792400e9f065
Quellennotizuspto-grants-2013_01