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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1024194Erstellt: 23. Oktober 2026

Sodium hydride → (1H-pyrrolo[2,3-b]pyridin-3-yl)-[6-(3-trifluoromethyl-benzyloxy)-pyridin-3-yl]-methanone

https://huagongshe.com/de/reaction/1024194

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
Edukt3-(Trifluoromethyl)benzylic alcoholHCID 67681—
Edukt(6-Chloro-pyridin-3-yl)-(1H-pyrrolo[2,3-b]pyridin-3-yl)-methanoneHCID 57588066—
LösungsmittelDimethyl SulfoxideHCID 679—
Produkt(1H-pyrrolo[2,3-b]pyridin-3-yl)-[6-(3-trifluoromethyl-benzyloxy)-pyridin-3-yl]-methanoneHCID 59593361—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

To (6-Chloro-pyridin-3-yl)-(1H-pyrrolo[2,3-b]pyridin-3-yl)-methanone 7 in DMSO was added (3-trifluoromethyl-phenyl)-methanol 72. Sodium hydride was added and the reaction was heated to 60° C. for two hours. The reaction was quenched with water and extracted with ethyl acetate. The organic portion was dried with magnesium sulfate and concentrated to provide (1H-pyrrolo[2,3-b]pyridin-3-yl)-[6-(3-trifluoromethyl-benzyloxy)-pyridin-3-yl]-methanone 73, which was used in the next step without additional purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08722702B2
Quelldatensatzuspto-grants-2014_05
ORD IDord-7593811251104b8d83f77363e00b04e7
Quellennotizuspto-grants-2014_05