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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 520612Erstellt: 26. Oktober 2026

Sodium Iodide → 6-(1H-Indol-4-yl)-4-[5-({4-[2-(4-morpholinyl)ethyl]-1-piperazinyl}methyl)-1,3,4-oxadiazol-2-yl]-1H-indazole

https://huagongshe.com/reaction/520612

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium IodideHCID 5238—
EduktSodium HydroxideHCID 14798—
EduktDiisopropylethylamineHCID 81531—
Edukt4-(2-Piperazin-1-yl-ethyl)-morpholineHCID 2734640—
Edukt4-[5-(Chloromethyl)-1,3,4-oxadiazol-2-yl]-6-(1H-indol-4-yl)-1-(phenylsulfonyl)-1H-indazoleHCID 66776954—
LösungsmittelIsopropanolHCID 3776—
LösungsmittelAcetonitrileHCID 6342—
Produkt6-(1H-Indol-4-yl)-4-[5-({4-[2-(4-morpholinyl)ethyl]-1-piperazinyl}methyl)-1,3,4-oxadiazol-2-yl]-1H-indazoleHCID 6677678150,5%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

4-[2-(1-piperazinyl)ethyl]morpholine (14.1 mg, 0.11 mmol) and 4-[5-(chloromethyl)-1,3,4-oxadiazol-2-yl]-6-(1H-indol-4-yl)-1-(phenylsulfonyl)-1H-indazole (50 mg, 0.102 mmol) were dissolved in acetonitrile (0.5 ml) and N,N-diisopropylethylamine (0.026 ml, 0.15 mmol) was added, followed by sodium iodide (15.3 mg, 0.102 mmol). The solution was stirred at 70° C. for 18 h and blown to dryness under a stream of nitrogen. Isopropanol (0.3 ml) was added followed by 2M sodium hydroxide (0.3 ml) and stirred for 5 h when the mixture was neutralised and the solvent removed under a stream of nitrogen. The crude product was dissolved in dimethylsulphoxide (0.3 ml) and methanol (0.15 ml) with formic acid (0.05 ml) then purified by Mass Directed Automated Preparative HPLC (Method F) to give the title compound (26.4 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09326987B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-ad3361f4e513427aa092b1e6b6cefb5b
Quellennotizuspto-grants-2016_05