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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2406339Erstellt: 25. Oktober 2026

2-Fluoro-4-(methylsulphonyl)benzeneboronic acid → 5-(2-Fluoro-4-methylsulfonyl-phenyl)-1''-tert-butoxycarbonyl-dispiro[2,3-dihydrofuro[2,3-c]pyridine-2,1'-cyclobutane-3',4''-piperidine]

https://huagongshe.com/reaction/2406339

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Fluoro-4-(methylsulphonyl)benzeneboronic acidHCID 44717666—
Edukt5-Chloro-1''-tert-butoxycarbonyl-dispiro[2,3-dihydrofuro[2,3-c]pyridine-2,1'-cyclobutane-3',4''-piperidine]HCID 86701200—
Produkt5-(2-Fluoro-4-methylsulfonyl-phenyl)-1''-tert-butoxycarbonyl-dispiro[2,3-dihydrofuro[2,3-c]pyridine-2,1'-cyclobutane-3',4''-piperidine]HCID 72194851—

Reaktionsschritte

The title compound is prepared from 5-chloro-1″-tert-butoxycarbonyl-dispiro[2,3-dihydrofuro[2,3-c]pyridine-2,1′-cyclobutane-3′,4″-piperidine] and 2-fluoro-4-methylsulfonyl-phenylboronic acid following a procedure analogous to that described for Example 2; PdCl2[1,1′-bis(diphenylphosphino)-ferrocene]*CH2Cl2 complex is the preferred catalyst used. LC (method 1): tR=1.30 min; Mass spectrum (ESI+): m/z=503 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08809361B2
Quelldatensatzuspto-grants-2014_08
ORD IDord-0415b58524f046688c01db62e607ed74
Quellennotizuspto-grants-2014_08