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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 494264Erstellt: 24. Oktober 2026

Sodium Carbonate → N-Quinolin-7-yl-6-(4-trifluoromethylphenyl)-nicotinamide

https://huagongshe.com/de/reaction/494264

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CarbonateHCID 10340—
Edukt4-(Trifluoromethyl)phenylboronic acidHCID 2734389—
Edukt6-Chloro-N-quinolin-7-yl-nicotinamideHCID 44578987—
KatalysatorHCID 178418397HCID 178418397—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
LösungsmittelEthyl AcetateHCID 8857—
ProduktN-Quinolin-7-yl-6-(4-trifluoromethylphenyl)-nicotinamideHCID 44578937—

Reaktionsschritte

To a solution of 6-chloro-N-quinolin-7-yl-nicotinamide (D70) (40 mg, 0.14 mmol) in DME (0.9 ml) under an argon atmosphere was added 4-trifluoromethylphenylboronic acid (33 mg, 0.17 mmol), 2M sodium carbonate solution (0.17 ml) and tetrakis(triphenylphosphine)palladium (0) (8 mg, 0.007 mmol). The reaction was heated at reflux until complete by tlc, then cooled to room temperature and diluted with EtOAc and dried over MgSO4. The solvent was removed in vacuo and the resultant crude product was purified by SPE column chromatography. Elution with 75% EtOAc in 40-60° C. petroleum ether gave the title compound as an off-white solid. 1H NMR (250 MHz, CDCl3) δ (ppm): 9.31 (dd, 1H), 8.83 (dd, 1H), 8.46 (dd, 1H), 8.39 (dd, 1H), 8.20 (m, 3H), 8.07 (d, 1H), 7.94 (dd, 1H), 7.89 (d, 1H), 7.79 (d, 2H), 7.40 (dd, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07538121B2
Quelldatensatzuspto-grants-2009_05
ORD IDord-3804f545fe4b4c91a07d363bb8bdb01c
Quellennotizuspto-grants-2009_05