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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 13129Erstellt: 24. Oktober 2026

Isobutyronitrile → (alphaS)-3-Fluoro-beta-[[1-(4-fluorophenyl)-1H-indazole-5-yl]oxy]-alpha-(2-methylpropyl)benzeneethanamine

https://huagongshe.com/de/reaction/13129

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIsobutyronitrileHCID 6559—
EduktCesium carbonateHCID 10796—
Edukt1-(4-fluorophenyl)-5-iodo-1H-indazoleHCID 59251128—
Edukt(2S)-2-Amino-1-(3-fluorophenyl)-4-methyl-pentane-1-olHCID 66812540—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Produkt(alphaS)-3-Fluoro-beta-[[1-(4-fluorophenyl)-1H-indazole-5-yl]oxy]-alpha-(2-methylpropyl)benzeneethanamineHCID 6681277323,3%

Reaktionsschritte

(2S)-2-Amino-1-(3-fluorophenyl)-4-methyl-pentane-1-ol (350 mg, 1.66 mmol), 5-iodo-1-(4-fluorophenyl)-1H-indazole (672.2 mg, 1.99 mmol), cesiumcarbonate (1.08 g, 3.31 mmol), copper (I)-iodide (157.8 mg, 0.83 mmol) and isobutyronitrile (1.75 mL) are stirred in a glass pressure tube at 120° C. for 20 h. The reaction mixture is filtered via a glass microfibre filter, the solvent evaporated and the residue purified by chromatography (silicagel, eluents: ethylacetate/methanol). 162.8 mg (23.3%) of the title compound are obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07728030B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-2f77677a013141f9a96d85bec8fd7e1c
Quellennotizuspto-grants-2010_06