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HRID 48940Erstellt: 23. Oktober 2026

Acetonitrile → 3,5-Dimethyl-2-phenylethynyl-3H-imidazole-4-carboxylic acid ethyl ester

https://huagongshe.com/de/reaction/48940

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetonitrileHCID 6342—
EduktTriethylamineHCID 8471—
EduktPhenylacetyleneHCID 10821—
Eduktethyl 2-bromo-1,4-dimethyl-1H-imidazole-5-carboxylateHCID 13897513—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelTrifluoroacetic acidHCID 6422—
Produkt3,5-Dimethyl-2-phenylethynyl-3H-imidazole-4-carboxylic acid ethyl esterHCID 983512629%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

In analogy to the method as described in Chem. Pharm. Bull. 1987, 35(2), 823-828, 17.5 mg (0.025 mmol) bis-(triphenylphosphine)-palladium-II-chloride, 2.9 mg (0.015 mmol) cuprous iodide, 60.5 mg (0.6 mmol) triethylamine, 32.4 mg (0.3 mmol) ethynylbenzene and 61.8 mg (0.25 mmol) 2-bromo-3,5-dimethyl-3H-imidazole-4-carboxylic acid ethyl ester are dissolved in 1 ml DMF and shaken for 3 h at 90° C. The title compound (19.3 mg, 29%, MS: m/e=269.3, [M+H+]) was isolated from the reaction mixture by HPLC chromatography (YMC CombiPrep C18 column 50×20 mm, solvent gradient 10-95% CH3CN in 0.1 % TFA(aq) over 6.0 min, λ=230 nm, flow rate 40 ml/min).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06706707B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-47219f08aa5c4ac497f38e43054e7af5
Quellennotizuspto-grants-2004_03