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HRID 1515911Erstellt: 26. Oktober 2026

5-(Trifluoromethyl)-3-((trimethylsilyl)ethynyl)-pyridin-2-amine → 5-Trifluoromethyl-1H-Pyrrolo[2,3-B]Pyridine

https://huagongshe.com/reaction/1515911

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-(Trifluoromethyl)-3-((trimethylsilyl)ethynyl)-pyridin-2-amineHCID 46736871—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
Produkt5-Trifluoromethyl-1H-Pyrrolo[2,3-B]PyridineHCID 3077211724%

Reaktionsbedingungen

Temperatur190 °C

Reaktionsschritte

5-Trifluoromethyl-3-trimethylsilanylethynyl-pyridin-2-ylamine (43.8 g, 170 mmol) and copper(I) iodide (6.5 g, 34 mmol) were dissolved in N-methylpyrrolidone (0.85 L). The mixture was stirred at 190° C. for 30 min. The mixture was evaporated to remove N-methylpyrrolidone in vacuo. The residue was purified by flash column chromatography (QingDao silical gel, 200-300 mesh, 40% ethyl acetate/hexanes) to afford 5-trifluoromethyl-1H-pyrrolo[2,3-b]pyridine (7.5 g, 24%) as a yellow solid: LC/MS m/e calcd for C8H5F3N2 [M+H]+ 187.14, observed 187.0.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08222416B2
Quelldatensatzuspto-grants-2012_07
ORD IDord-9d5065a2826d4c28b1cb2aaf175463c2
Quellennotizuspto-grants-2012_07