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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 62533Erstellt: 24. Oktober 2026

Pentapotassium Triphosphate → 5-Chloro-2-[(2,5-dichloro-4-pyridinyl)amino]benzonitrile

https://huagongshe.com/de/reaction/62533

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPentapotassium TriphosphateHCID 61695—
Edukt2-Amino-5-chlorobenzonitrileHCID 80019—
EduktBis[2-(diphenylphosphino)phenyl] etherHCID 4285986—
Edukt2,5-Dichloro-4-iodopyridineHCID 53400965—
Katalysatorpalladium(II) acetateHCID 167845—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt5-Chloro-2-[(2,5-dichloro-4-pyridinyl)amino]benzonitrileHCID 5751691733%

Reaktionsschritte

To a degassed solution of 2,5-dichloro-4-iodopyridine (4.5 g, 16.43 mmol), 2-amino-5-chlorobenzonitrile (2.507 g, 16.43 mmol) and potassium triphosphate (10.46 g, 49.3 mmol) in 1,4-dioxane (60 ml) stirred under nitrogen at the room temperature was added DPEPhos (0.708 g, 1.314 mmol) and palladium acetate (0.148 g, 0.657 mmol). The reaction mixture was stirred at reflux for 18 hr. The reaction mixture was filtered. The reaction mixture was evaporated. Ether (50 ml) was added and the solid was filtered. 5-chloro-2-[(2,5-dichloro-4-pyridinyl)amino]benzonitrile (1.8 g, 5.43 mmol, 33.0% yield) was isolated as orange solid. 1H NMR (400 MHz, DMSO-d6) ppm 6.63 (s, 1 H) 7.52 (d, J=8.59 Hz, 1 H) 7.81 (dd, J=8.59, 2.53 Hz, 1 H) 8.09 (d, J=2.53 Hz, 1 H) 8.24 (s, 1 H) 9.06 (br. s., 1 H); HPLC Rt=3.53 min, MS (ESI): 298.0, 299.9 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09446034B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-54da0cd2dccb47709c1b181e15a3543d
Quellennotizuspto-grants-2016_09