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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pentapotassium Triphosphate | HCID 61695 | — |
| Reactant | Benzonitrile, 2-amino-4-chloro- | HCID 170059 | — |
| Reactant | Bis[2-(diphenylphosphino)phenyl] ether | HCID 4285986 | — |
| Reactant | 2,5-Dichloro-4-iodopyridine | HCID 53400965 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-Chloro-2-[(2,5-dichloro-4-pyridinyl)amino]benzonitrile | HCID 57516916 | 57.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09012479B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-9b915b4781aa4fc9b8abb5a68bcc2326 |
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| Source note | uspto-grants-2015_04 |
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