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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1717134Erstellt: 25. Oktober 2026

(3-Chlorophenyl)boronic acid → {3-[(3'-Chloro-4-fluoro-biphenyl-3-carbonyl)-amino]-phenoxy}-acetic acid

https://huagongshe.com/reaction/1717134

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(3-Chlorophenyl)boronic acidHCID 2734323—
Edukt[3-(5-Bromo-2-fluoro-benzoylamino)-phenoxy]-acetic acid ethyl esterHCID 40356283—
Produkt{3-[(3'-Chloro-4-fluoro-biphenyl-3-carbonyl)-amino]-phenoxy}-acetic acidHCID 59654666—

Reaktionsschritte

The phenyl bromide (139) (50 mg, 0.13 mmol) was coupled to 3-chloro-phenylboronic acid (20 mg, 0.13 mmol) using Method E. During this reaction, hydrolysis occurred and the residue was extracted using Work-up E1. The crude product was then triturated with TBME (2 ml), DCM (2 ml), and recrystallised from a hot 10% EtOH in H2O mixture to give the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07803841B2
Quelldatensatzuspto-grants-2010_09
ORD IDord-9f28926e9c204dc6aef4eb6c0da4a8e0
Quellennotizuspto-grants-2010_09