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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62537Generated: October 26, 2026

Pentapotassium Triphosphate → 2-[(2,5-Dichloro-4-pyridinyl)amino]-5-fluorobenzonitrile

https://huagongshe.com/reaction/62537

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPentapotassium TriphosphateHCID 61695—
Reactant2-Amino-5-fluorobenzonitrileHCID 2737704—
Reactant2,5-Dichloro-4-iodopyridineHCID 53400965—
Catalystpalladium(II) acetateHCID 167845—
CatalystBis[2-(diphenylphosphino)phenyl] etherHCID 4285986—
Solvent1,4-DioxaneHCID 31275—
Product2-[(2,5-Dichloro-4-pyridinyl)amino]-5-fluorobenzonitrileHCID 5751691886%

Reaction Steps

To a degassed solution of 2,5-dichloro-4-iodopyridine (8 g, 29.2 mmol), 2-amino-5-fluorobenzonitrile (3.98 g, 29.2 mmol) and potassium triphosphate (18.60 g, 88 mmol) in 1,4-dioxane (100 ml) stirred under nitrogen at the room temperature was added DPEPhos (1.258 g, 2.337 mmol) and palladium acetate (0.262 g, 1.168 mmol). The reaction mixture was stirred at the reflux for 18 hr. The reaction mixture was filtered. The solvent was evaporated. Ether (50 ml) was added and the solid was filtered. 2-[(2,5-Dichloro-4-pyridinyl)amino]-5-fluorobenzonitrile (7.09 g, 25.1 mmol, 86% yield) was isolated as an orange solid. 1H NMR (400 MHz, METHANOL-d4) ppm 6.44 (s, 1 H) 7.46-7.58 (m, 2 H) 7.66 (dd, J=8.08, 2.78 Hz, 1 H) 8.08 (s, 1 H); HPLC Rt=3.23 min, MS (ESI): 382.0, 384.19 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09446034B2
Source datasetuspto-grants-2016_09
ORD IDord-96223665d9f24db18761ea870c899c22
Source noteuspto-grants-2016_09