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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 407237Erstellt: 24. Oktober 2026

Potassium Fluoride → Methyl 4-amino-6-(4-chlorophenyl)-5-fluoro-3-methoxypicolinate

https://huagongshe.com/de/reaction/407237

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium FluorideHCID 522689—
Edukt2-(4-Chlorophenyl)-1,3,2-dioxaborinaneHCID 3468957—
EduktTrisodium 3,3',3''-phosphinetriyltris(benzene-1-sulphonate)HCID 6099338—
EduktMethyl 4-amino-6-chloro-5-fluoro-3-methoxypicolinateHCID 86675409—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelWaterHCID 962—
LösungsmittelAcetonitrileHCID 6342—
LösungsmittelDichloromethaneHCID 6344—
ProduktMethyl 4-amino-6-(4-chlorophenyl)-5-fluoro-3-methoxypicolinateHCID 7115069672,2%

Reaktionsbedingungen

Temperatur150 °C

Reaktionsschritte

To a solution of methyl 4-amino-6-chloro-5-fluoro-3-methoxypicolinate (200 mg, 0.852 mmol) in CH3CN (1.246 mL) and H2O (1.246 mL) were added 2-(4-chlorophenyl)-1,3,2-dioxaborinane (251 mg, 1.279 mmol), KF (149 mg, 2.56 mmol), palladium(II) acetate (Pd(OAc)2; 19.14 mg, 0.085 mmol), and triphenylphosphine-3,3′,3″-trisulfonic acid trisodium salt (100 mg, 0.170 mmol). The reaction mixture was then heated in a bench top Biotage microwave at 150° C. for 5 min. The reaction mixture was diluted with CH2Cl2 and washed with H2O. The organic layer was separated, dried over MgSO4, filtered and concentrated. The crude residue was purified by normal phase chromatography (eluting with 10% EtOAc/40% CH2Cl2/50% hexanes) to afford the title compound as a tan solid (191 mg, 72.1%): mp 93-94° C.; 1H NMR (400 MHz, acetone-d6) δ 7.96 (dd, J=8.8, 1.4 Hz, 2H), 7.57-7.49 (m, 2H), 5.93 (s, 2H), 3.92 (s, 3H), 3.91 (s, 3H), ESIMS m/z 311 ([M+H]+), 309 ([M−H]−).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08754229B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-9c18d074a7144da5a2d778269b02827d
Quellennotizuspto-grants-2014_06