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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 259Erstellt: 23. Oktober 2026

4-Fluoro-N-methylaniline → 5-bromo-N-(4-fluorophenyl)-N-methylpyridin-3-amine

https://huagongshe.com/de/reaction/259

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Fluoro-N-methylanilineHCID 68024—
Edukt3,5-DibromopyridineHCID 69369—
ReagenzCesium carbonateHCID 10796—
Katalysator2-(Dicyclohexylphosphino)biphenylHCID 2734216—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
LösungsmittelTolueneHCID 1140—
Produkt5-bromo-N-(4-fluorophenyl)-N-methylpyridin-3-amineHCID 1045316970%

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

In a 50 mL round-bottomed flask (t=g) was 4-fluoro-N-methylaniline (.05 g, 0.40 mmol), 3,5-dibromopyridine (0.114 g, 0.48 mmol), and Pd2(dba)3 (0.018 g, 0.02 mmol) in toluene (16 mL) ([VOLUME]) to give a purple suspension. biphenyl-2-yldicyclohexylphosphine (0.021 g, 0.06 mmol) and CS2CO3 (0.195 g, 0.60 mmol) were added. After LC/MS indicated no reaction had taken place at room temp, the temperature was gradually rasied to up to 110 degrees. LC/MS indicated that the reaction was not progressing. Reaction was discarded.

Herkunft & Nachweise

Quelldatensatz750 AstraZeneca ELN dataset
ORD IDord-d1bfb220e27441fcb5908d58a9e8690c
Quellennotiz750 AstraZeneca ELN dataset