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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 19864Erstellt: 23. Oktober 2026

3-Cyanophenylboronic acid → 3-[2-(4,4-Difluoro-piperidine-1-carbonyl)-5-(1-isopropyl-piperidin-4-yloxy)-indol-1-yl]-benzonitrile

https://huagongshe.com/de/reaction/19864

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Cyanophenylboronic acidHCID 2734325—
Edukt(4,4-Difluoropiperidin-1-yl)[5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]methanoneHCID 11603838—
Produkt3-[2-(4,4-Difluoro-piperidine-1-carbonyl)-5-(1-isopropyl-piperidin-4-yloxy)-indol-1-yl]-benzonitrileHCID 16739528—

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-cyanophenylboronic acid. The title compound was obtained in 46% yield as yellow foam. MS (m/e): 507.3 (MH+, 100%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745479B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-5002c25decad4be9ae66d0efbe0bb9bb
Quellennotizuspto-grants-2010_06