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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1727870Erstellt: 26. Oktober 2026

Water → (4-Tert-butylcyclohexyl)-[4-(6,7-dimethoxyquinolin-4-yloxy)phenyl]amine

https://huagongshe.com/reaction/1727870

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt4-tert-ButylcyclohexanoneHCID 7392—
EduktSodium triacetoxyborohydrideHCID 5049666—
Edukt4-[(6,7-Dimethoxyquinolin-4-yl)oxy]anilineHCID 11594543—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
Produkt(4-Tert-butylcyclohexyl)-[4-(6,7-dimethoxyquinolin-4-yloxy)phenyl]amineHCID 1011379511,4%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

4-(6,7-Dimethoxy-4-quinolyloxy)aniline (300 mg) was dissolved in N,N-dimethylformamide (10 ml) to prepare a solution. 4-Tert-butylcyclohexanone (200 mg) was then added to the solution, and the mixture was stirred at 60° C. for one hr. The reaction solution was cooled to room temperature before sodium triacetoxy borohydride (400 mg) was added thereto. The mixture was then stirred at room temperature for 3 hr. Water and ethyl acetate were added to the reaction solution, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine and was dried over sodium sulfate. The solvent was removed by evaporation under the reduced pressure, and the residue was purified by chromatography on silica gel using chloroform/acetone for development to give the title compound (50 mg, yield 11%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07495104B2
Quelldatensatzuspto-grants-2009_02
ORD IDord-0d993d71c9dd4f9da18e2a28b9b43173
Quellennotizuspto-grants-2009_02