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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1984640Erstellt: 26. Oktober 2026

Triethylamine → 2-(5-Methyl-3-phenyl-isoxazol-4-ylethynyl)-pyridine

https://huagongshe.com/reaction/1984640

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt1,3-Bis(diphenylphosphino)propaneHCID 81219—
EduktEthynylpyridineHCID 137268—
Edukt4-Iodo-5-methyl-3-phenylisoxazoleHCID 2776150—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-(5-Methyl-3-phenyl-isoxazol-4-ylethynyl)-pyridineHCID 2478444623,1%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

A mixture of 4-iodo-5-methyl-3-phenylisoxazole (285 mg, 1.00 mmol), palladium(II) acetate (7 mg, 0.03 mmol), 1,3-bis(diphenylphosphino)propane (12 mg, 0.03 mmol), triethylamine (348 μL, 2.50 mmol) and 2-ethynylpyridine (131 μL, 1.30 mmol) in N,N-dimethylformamide (2 mL) was evaporated and flushed with argon. Cuprous iodide (4 mg, 0.02 mmol) was added and the reaction mixture was stirred for 3 h at 90° C. before cooling to ambient temperature and separated between aqueous sodium hydroxide (1 M, 30 mL) and ethyl acetate (50 mL). The aqueous layer was extracted with ethyl acetate (50 mL) and washed with aqueous sodium hydroxide (1 M, 30 mL). The combined organic layers were dried over sodium sulfate and concentrated. Purification by chromatography (SiO2, heptane:ethyl acetate=100:0 to 67:33) afforded the title compound (60 mg, 23%) as a light brown solid. MS: m/e=261.2 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07544704B2
Quelldatensatzuspto-grants-2009_06
ORD IDord-cfb5c6edebff49b29fea7c3ae5467541
Quellennotizuspto-grants-2009_06