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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1472576Generated: October 26, 2026

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

https://huagongshe.com/reaction/1472576

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPentapotassium TriphosphateHCID 61695—
ReactantBenzonitrile, 2-amino-4-chloro-HCID 170059—
ReactantBis[2-(diphenylphosphino)phenyl] etherHCID 4285986—
Reactant2,5-Dichloro-4-iodopyridineHCID 53400965—
Catalystpalladium(II) acetateHCID 167845—
Solvent1,4-DioxaneHCID 31275—
Product4-Chloro-2-[(2,5-dichloro-4-pyridinyl)amino]benzonitrileHCID 5751691657.1%

Reaction Steps

To a degassed solution of 2,5-dichloro-4-iodopyridine (4.5 g, 16.43 mmol), 2-amino-4-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 the reflux for 18 hr. The reaction mixture was filtered. The solution was evaporated. Ether (50 ml) was added and the formed solid was filtered. 4-chloro-2-[(2,5-dichloro-4-pyridinyl)amino]benzonitrile (2.8 g, 9.38 mmol, 57.1% yield) was isolated as an orange solid. 1H NMR (400 MHz, DMSO-d6) ppm 6.70 (s, 1 H) 7.53 (dd, J=8.34, 2.02 Hz, 1 H) 7.65 (d, J=2.02 Hz, 1 H) 7.95 (d, J=8.34 Hz, 1 H) 8.28 (s, 1 H) 9.12 (br. s., 1 H); HPLC Rt=3.50 min, MS (ESI): 298.0, 300.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012479B2
Source datasetuspto-grants-2015_04
ORD IDord-9b915b4781aa4fc9b8abb5a68bcc2326
Source noteuspto-grants-2015_04