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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 25618Erstellt: 24. Oktober 2026

Imidazole → HCID 178463970, Verbindung

https://huagongshe.com/de/reaction/25618

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktImidazoleHCID 795—
Edukttert-Butyldimethylsilyl chlorideHCID 28928—
EduktSodium BicarbonateHCID 516892—
EduktHCID 178464455HCID 178464455—
LösungsmittelTolueneHCID 1140—
LösungsmittelDimethylformamideHCID 6228—
ProduktHCID 178463970HCID 17846397010,2%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

400 mg (8.4 mmol) trans-N-(4-{5-[Ethyl-(2-hydroxy-ethyl)-amino]-pentyl}-cyclohexyl)-N-methyl-4-trifluoromethyl-benzenesulfonamide were suspended in toluene and evaporated (3×), redissolved in lml DMF and treated with 102.4 mg (1.5 mmol, 1.8 eq) imidazole. At 0° C., 176 mg (11.7 mmol, 1.4 eq) TBDMSCl in 2 ml DMF were added, and the reaction mixture was stirred at 50° C. for 1 h. The solution was added to an aqueous solution of NaHCO3 and extracted with ether. The organic layer was washed with water and brine, and dried over Na2SO4. 509 mg crude trans-N-[4-(5-{[2-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-ethyl-amino}-pentyl)-cyclohexyl]-N-methyl-4-trifluoromethyl-benzenesulfonamide were isolated as light yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06858651B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-cc39c75da0944473b4915be6d02ba9a7
Quellennotizuspto-grants-2005_02