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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 232875Erstellt: 24. Oktober 2026

2-(7-Chloro-6-fluoroquinolin-2-yl)methoxy-11-oxo-6,11-dihydrodibenz[b,e]oxepine → 2-(7-Chloro-6-fluoroquinolin-2-yl)methoxy-11-hydroxy-6,11-dihydrodibenz[b,e]oxepine

https://huagongshe.com/de/reaction/232875

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-(7-Chloro-6-fluoroquinolin-2-yl)methoxy-11-oxo-6,11-dihydrodibenz[b,e]oxepineHCID 23359142—
EduktHCID 178418435HCID 178418435—
LösungsmittelMethanolHCID 887—
Produkt2-(7-Chloro-6-fluoroquinolin-2-yl)methoxy-11-hydroxy-6,11-dihydrodibenz[b,e]oxepineHCID 2335913472,1%

Reaktionsschritte

0.5 g of sodium boron hydride was added to 2.58 g of 2-(7-chloro-6-fluoroquinolin-2-yl)methoxy-11-oxo-6,11-dihydrodibenz[b,e]oxepine obtained in Reference example 34 suspended in 70 ml of methanol and the mixture was stirred at room temperature for 11 hours. During stirring, 0.35 g of sodium boron hydride was added to the mixture twice. After completion of the reaction, the solvent was removed under reduced pressure, ice water was added to the residue and the mixture was extracted with methylene chloride. Then, the organic layer was washed with water and then dried over anhydrous sodium sulfate and the solvent was removed. The resulting solid was washed with a methylene chloride-hexane mixed solution to obtain 1.87 g of the title compound. Mass (CI); m/z=422 (M+ +1)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05591752
Quelldatensatzuspto-grants-1997_01
ORD IDord-de0b38d424da4514b19f65882da930be
Quellennotizuspto-grants-1997_01