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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1472579Generated: October 26, 2026

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

https://huagongshe.com/reaction/1472579

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPentapotassium TriphosphateHCID 61695—
Reactant2-Amino-5-chlorobenzonitrileHCID 80019—
ReactantBis[2-(diphenylphosphino)phenyl] etherHCID 4285986—
Reactant2,5-Dichloro-4-iodopyridineHCID 53400965—
Catalystpalladium(II) acetateHCID 167845—
Solvent1,4-DioxaneHCID 31275—
Product5-Chloro-2-[(2,5-dichloro-4-pyridinyl)amino]benzonitrileHCID 5751691733%

Reaction Steps

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]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012479B2
Source datasetuspto-grants-2015_04
ORD IDord-57d09e4e255d40ec898f52c23eb112ae
Source noteuspto-grants-2015_04