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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 512488Erstellt: 23. Oktober 2026

2-(Trifluoromethyl)pyridine-4-boronic acid → 1-[1-(4-Cyano-phenyl)-ethyl]-2-methyl-4-oxo-2'-trifluoromethyl-1,4-dihydro-[3,4']bipyridinyl-5-carboxylic acid

https://huagongshe.com/de/reaction/512488

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-(Trifluoromethyl)pyridine-4-boronic acidHCID 45158880—
Edukt1-(4-Cyano-benzyl)-6-methyl-4-oxo-5-(3-trifluoromethyl-phenyl)-1,4-dihydro-pyridine-3-carboxylic acidHCID 86711527—
Edukt5-Bromo-1-(4-cyano-benzyl)-6-methyl-4-oxo-1,4-dihydro-pyridine-3-carboxylic acidHCID 86711528—
Edukt5-Bromo-1-[1-(4-cyano-phenyl)-ethyl]-6-methyl-4-oxo-1,4-dihydro-pyridine-3-carboxylic acidHCID 86711530—
Produkt1-[1-(4-Cyano-phenyl)-ethyl]-2-methyl-4-oxo-2'-trifluoromethyl-1,4-dihydro-[3,4']bipyridinyl-5-carboxylic acidHCID 86711531—

Reaktionsschritte

Preparation 4 is prepared following the procedure described for preparation 1d, substituting 3-(trifluoromethyl)phenylboronic acid with 2-(trifluoromethyl)pyridine-4-boronic acid and substituting preparation 1c with preparation 2b as starting material. ESI mass spectrum: [M+H]+=428; Retention time HPLC: 0.99 min (Z018_S04).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09102624B2
Quelldatensatzuspto-grants-2015_08
ORD IDord-cd409417a5054a9d81a2c873f0f2f97a
Quellennotizuspto-grants-2015_08