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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 724214Erstellt: 26. Oktober 2026

Toluene → N,N-diisopropyl-6-[(1-trityl-1H-imidazol-4-yl)carbonyl]-2-naphthamide

https://huagongshe.com/reaction/724214

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
EduktTetrahydrofuranHCID 8028—
Edukt6-bromo-N,N-diisopropyl-2-naphthamideHCID 21879639—
EduktN-Methyl-N-methoxy-2-(1-triphenylmethyl-1H-imidazol-4-yl)acetamideHCID 54243787—
EduktButyllithiumHCID 178418339—
LösungsmittelWaterHCID 962—
ProduktN,N-diisopropyl-6-[(1-trityl-1H-imidazol-4-yl)carbonyl]-2-naphthamideHCID 21879613—

Reaktionsbedingungen

Temperatur-70 °C

Reaktionsschritte

Dry toluene (20 ml) was cooled to −70° C. and n-butyl lithium (1.6 M; 2.35 ml) was added dropwise. A solution of 6-bromo-N,N-diisopropyl-2-naphthamide (1.20 g) in dry THF (8 ml) was added dropwise to the reaction mixture. After stirring the mixture at −70° C. for 20 min, a solution of N-methoxy-N-methyl-1-trityl-1H-imidazole-4-carboxyamide (1.09 g) in dry THF (6 ml) was added dropwise to the reaction mixture. The mixture was stirred at −70° C. for 20 min and water was added at the same temperature to stop the reaction. The mixture was extracted with ethyl acetate, and the organic layer was washed with saturated brine and dried over magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by column chromatography (hexane:ethyl acetate=2:1) to give the title compound (1.40 g) as a colorless powder. The physical and chemical data were identical with those obtained for the compound obtained of Reference Example 13.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07141598B2
Quelldatensatzuspto-grants-2006_11
ORD IDord-f83ff25fe42847548c13016112ee2d90
Quellennotizuspto-grants-2006_11