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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 19854Erstellt: 26. Oktober 2026

3-Fluorophenylboronic acid → (4,4-Difluoro-piperidin-1-yl)-[1-(3-fluoro-phenyl)-5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-methanone

https://huagongshe.com/reaction/19854

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Fluorophenylboronic acidHCID 2733986—
Edukt(4,4-Difluoropiperidin-1-yl)[5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]methanoneHCID 11603838—
Produkt(4,4-Difluoro-piperidin-1-yl)-[1-(3-fluoro-phenyl)-5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-methanoneHCID 16739444—

Reaktionsschritte

In analogy to the procedure described for the synthesis of example 6, the title compound was synthesized from (4,4-difluoro-piperidin-1-yl)-[5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-methanone (intermediate 1) and 3-fluorobenzeneboronic acid. The title compound was obtained in 97% yield as yellow foam. MS (m/e): 500.1 (MH+, 100%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745479B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-4166aa5584244dbf94d7afcf1d04cac5
Quellennotizuspto-grants-2010_06