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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 877307Erstellt: 25. Oktober 2026

1-Methyl-1,4-cyclohexadiene → (R)-5-(2-Amino-1-hydroxyethyl)-8-hydroxyquinolin-2(1H)-one hydrochloride

https://huagongshe.com/reaction/877307

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Methyl-1,4-cyclohexadieneHCID 78006—
Edukt1,4-Dioxane hydrochlorideHCID 20443148—
Edukt(R)-5-(2-Azido-1-((tert-butyldimethylsilyl)oxy)ethyl)-8-(benzyloxy)quinolin-2(1H)-oneHCID 58505233—
KatalysatorPalladiumHCID 23938—
LösungsmittelEthanolHCID 702—
Produkt(R)-5-(2-Amino-1-hydroxyethyl)-8-hydroxyquinolin-2(1H)-one hydrochlorideHCID 7109324164,3%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

To a solution of (R)-5-(2-azido-1-((tert-butyldimethylsilyl)oxy)ethyl)-8-(benzyloxy)quinolin-2(1H)-one (4.50 g, 10.0 mmol) in ethanol (50 mL) was added 10% palladium on charcoal (4.50 g) followed by 1-methyl-1,4-cyclohexadiene (11.0 mL, 97.9 mmol). The reaction was warmed to 60° C. and then stirred at 60° C. for 2 hours. The reaction mixture was allowed to cool and filtered through a pad of celite. The filtercake was washed with further ethanol and the filtrate was evaporated at reduced pressure. The residue was evaporated from iso-propanol (×2) and dissolved in iso-propanol (30 mL). HCl-dioxane (4 M, 50 mL, 200 mmol) was added and the reaction mixture stirred at RT for 18 hours. The resultant suspension was filtered, the filtercake washed with ether and the solid dried under vacuum in the presence of P2O5 to afford the title compound (1.65 g, 62%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08987299B2
Quelldatensatzuspto-grants-2015_03
ORD IDord-7560b14e50c94fc5b482526f2bbd4b60
Quellennotizuspto-grants-2015_03