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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 29507Erstellt: 23. Oktober 2026

Hydrochloric Acid → (2-Amino-4,5-difluoro-phenyl)-pyridin-4-yl-methanone

https://huagongshe.com/de/reaction/29507

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt4-CyanopyridineHCID 7506—
EduktSodium HydroxideHCID 14798—
EduktBoron TrichlorideHCID 25135—
Edukt3,4-DifluoroanilineHCID 77469—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTrichloroethyleneHCID 6575—
Produkt(2-Amino-4,5-difluoro-phenyl)-pyridin-4-yl-methanoneHCID 22327317—

Reaktionsschritte

BCl3 (6.2 ml, 1M in DCM) was added drop wise to 1,2-difluoro-4aminobenzene (0.5 g, 0.004 mol) in trichloroethylene (6.5 ml) at 0° C. and this mixture stirred for 15 min. 4-Cyanopyridine (0.48 g, 0.005 mol) was added and the solution was warmed to RT and stirred for 30 min. The solution was then heated at 80-90° C. for 1 h. The resulting solution was refluxed at 160° C. for 4 hr and stirred at RT over night. 3N HCl was added to the reaction mixture and refluxed at 110° C. for 1.5 h. The reaction mixture was cooled to RT and made basic (pH=12) with 6N NaOH. The reaction mixture was diluted with water and DCM. The resulting two layers were separated and the aqueous layer was extracted with DCM, dried over sodium sulphate and concentrated. The compound was purified by column chromatography using silica gel to yield title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07420055B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-590fb90e5aed4c9387b4cf70831341c8
Quellennotizuspto-grants-2008_09