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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 9898Erstellt: 23. Oktober 2026

Isopropyl iodide → 2-Chloro-N-(3-chlorophenyl)-9-isopropyl-9H-purin-6-amine

https://huagongshe.com/de/reaction/9898

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIsopropyl iodideHCID 6362—
EduktCesium carbonateHCID 10796—
Edukt2-chloro-N-(3-chlorophenyl)-9H-purin-6-amineHCID 21988232—
LösungsmittelEthyl AcetateHCID 8857—
Lösungsmittel1,4-DioxaneHCID 31275—
LösungsmittelN,N-Dimethylformamide--water (1/1)HCID 21962138—
Produkt2-Chloro-N-(3-chlorophenyl)-9-isopropyl-9H-purin-6-amineHCID 21988248—

Reaktionsschritte

500 mg (1.78 mmol) of 2-chloro-6-(3-chloro-phenyl-amino)-purine are dissolved in a mixture of 29.5 ml of DMF/water (85/15) and 5 ml of dioxane by means of gentle heating. 870 mg (2.67 mmol) of caesium carbonate, followed by 1.78 ml (17.8 mmol) of isopropyl iodide are added at room temperature. The reaction mixture is stirred at room temperature for 18 hours. To bring the reaction to completion, the reaction mixture is stirred at 45° C. for a further 24 hours. When the reaction has ended, the reaction mixture is diluted with ethyl acetate, washed with water (2 times) and saturated sodium chloride solution and dried over magnesium sulfate. After filtration, the filtrate is concentrated under reduced pressure at 35° C. and the residue is dried under an HV. The resulting crude product is purified by crystallization from diethyl ether/hexane. 2-Chloro-6-(3-chloro-phenyl-amino)-9-isopropyl-9H-purine is obtained; Rf=0.46 (ethyl acetate); m.p. 128–129° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07091346B1
Quelldatensatzuspto-grants-2006_08
ORD IDord-74fde67f2a9f47cb945db7fa6bea0160
Quellennotizuspto-grants-2006_08