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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1028967Erstellt: 26. Oktober 2026

Potassium Acetate → Cyclopentyl 2-(2-amino-3-morpholinoquinolin-6-yl)-3-methylbenzoate

https://huagongshe.com/reaction/1028967

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium AcetateHCID 517044—
Edukt2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
EduktCyclopentyl 2-bromo-3-methylbenzoateHCID 67325920—
Edukt3-Morpholino-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinolin-2-amineHCID 67347995—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
ProduktCyclopentyl 2-(2-amino-3-morpholinoquinolin-6-yl)-3-methylbenzoateHCID 53328993—

Reaktionsbedingungen

Temperatur145 °C

Reaktionsschritte

3-Morpholino-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinolin-2-amine (0.15 g, 0.422 mmol, prepared as Example 2, Step 1-2), cyclopentyl 2-bromo-3-methylbenzoate (0.133 g, 0.470 mmol), potassium acetate (0.079 mL, 1.267 mmol), 2-dicyclohexylphosphino-2′,4′,6′,-triisopropylbiphenyl (0.020 g, 0.042 mmol), palladium(II) acetate (4.74 mg, 0.021 mmol), water (0.3 mL) and ethanol (2 mL) were combined in a microwave vial and heated to 145° C. for 30 min. The crude material was partitioned between water (40 mL) and DCM (50 mL). The organic layer was dried on magnesium sulfate, filtered and concentrated. The crude material was purified by silica chromatography (0-10% methanol in DCM gradient) to give cyclopentyl 2-(2-amino-3-morpholinoquinolin-6-yl)-3-methylbenzoate. MS (ESI, pos. ion) m/z: 432 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08735384B2
Quelldatensatzuspto-grants-2014_05
ORD IDord-dadcf29bce2b4d44a8e9b291984471e2
Quellennotizuspto-grants-2014_05