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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 73Erstellt: 23. Oktober 2026

4-Aminobenzonitrile → HCID 178418220, Verbindung

https://huagongshe.com/de/reaction/73

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-AminobenzonitrileHCID 13396—
Edukt6-chloro-N-cyclohexylpyridine-3-carboxamideHCID 857493—
ReagenzPotassium tert-butoxideHCID 23665647—
KatalysatorBinap, (A+-)-HCID 634876—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktHCID 178418220HCID 1784182209,93%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

In a 50 mL round-bottomed flask a TRIS(DIBENZYLIDENEACETONE)DIPALLADIUM(0) (0.115 g, 0.13 mmol),POTASSIUM TERT-BUTOXIDE (0.282 g, 2.51 mmol)and BINAP (0.157 g, 0.25 mmol) in dry 1,4-dioxane (10 mL) was mixed under N2.Followed by 6-chloro-N-cyclohexylnicotinamide (.300 g, 1.26 mmol) and 4-aminobenzonitrile (0.178 g, 1.51 mmol) was added and resulting mixture(dark brown) was heated at 100oC for 3 hrs.LCMS analysis showed the formation of required product.Reaction stopped,crude was passed through celite and washed with dioxane and finally with methanol.The filtrate was dried and dissolved in 3 ml DMSO for Waters MS Purification system.Pure fractions collected and concentrated.A White solid obtained as a product 6-(4-cyanophenylamino)-N-cyclohexylnicotinamide (0.040 g, 9.93 %).32 mg of above product was submitted for MGyrx2 projetct.LCMS/NMR confirmed the product.

Herkunft & Nachweise

Quelldatensatz750 AstraZeneca ELN dataset
ORD IDord-2d4104aef43247ff855d465ce3910528
Quellennotiz750 AstraZeneca ELN dataset