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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 659938Erstellt: 24. Oktober 2026

Triethylamine → Dimethyl-(2-pyridin-4-ylethynyl-pyridin-3-yl)-amine

https://huagongshe.com/de/reaction/659938

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktAmmonium ChlorideHCID 25517—
Edukt4-EthynylpyridineHCID 642801—
Edukt2-bromo-N,N-dimethylpyridin-3-amineHCID 86643498—
KatalysatorCopper iodideHCID 83717—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelDimethylformamideHCID 6228—
ProduktDimethyl-(2-pyridin-4-ylethynyl-pyridin-3-yl)-amineHCID 6842928445%

Reaktionsschritte

A mixture of 2 g of (2-Bromo-pyridin-3-yl)-dimethyl-amine (9.95 mmoles), 1.24 g of 4-ethynyl pyridine (12 mmoles) in 120 mL of a 1/1 mixture of triethylamine and dimethylformamide is stirred under argon at room temperature. 750 mg of bis(triphenylphosphine)palladium dichloride and 400 mg of copper iodide are added to the reaction mixture which is further stirred at room temperature for 3 hours. The reaction mixture is poured into ammonium chloride solution and extracted with ethyl acetate. The organic phase is washed with water and dried over magnesium sulfate. The solid residue after concentration is purified by chromatography on silica gel (ethylacetate/hexane 1/1) to give 1 g of Dimethyl-(2-pyridin-4-ylethynyl-pyridin-3-yl)-amine as orange oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08084395B2
Quelldatensatzuspto-grants-2011_12
ORD IDord-4951c305bfd4457389ec8e82d453e684
Quellennotizuspto-grants-2011_12