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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 19556Erstellt: 24. Oktober 2026

Triphenylphosphine → 6-(2-morpholine-4-ylethoxy)-1-oxo-3-pheny-1H-indene-2-carboxylic acid cyclohexylamide

https://huagongshe.com/de/reaction/19556

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriphenylphosphineHCID 11776—
Edukt2-MorpholinoethanolHCID 61163—
EduktDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Edukt6-hydroxy-1-oxo-3-phenyl-1H-indene-2-carboxylic acid cyclohexylamideHCID 68697166—
LösungsmittelTetrahydropyran benzeneHCID 86615313—
Produkt6-(2-morpholine-4-ylethoxy)-1-oxo-3-pheny-1H-indene-2-carboxylic acid cyclohexylamideHCID 6869834988,3%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

6-Hydroxy-1-oxo-3-phenyl-1H-indene-2-carboxylic acid cyclohexylamide (141 mg, 0.41 mmol) obtained in Step 3 was dissolved in tetrahydropyran/benzene (3 mL/2 mL), and 4-(2-hydroxyethyl)morpholine (99 μl, 0.82 mmol) and triphenylphosphine (215 mg, 0.82 mmol) were added thereto. Then, diisopropyl azodicarboxilate (149 μl, 0.82 mmol) was added slowly thereto at 0° C., and stirred for 2 hrs at RT. The resulting mixture washed with saturated saline and extracted with ethyl acetate. The organic layer was separated, dried over anhydrous MgSO4 and concentrated under a reduced pressure. The resulting residue was purified by flash chromatography to obtain 165 mg of the titled compound (yield: 88.3%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745439B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-e8d480256d7b46968a7d67c25afe805a
Quellennotizuspto-grants-2010_06