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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 10560Erstellt: 24. Oktober 2026

Water → 4-(4-Methoxy-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidine

https://huagongshe.com/de/reaction/10560

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium MethoxideHCID 10942334—
Edukt4-(4-Bromo-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidineHCID 21979972—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelMethanolHCID 887—
LösungsmittelPyridineHCID 1049—
Produkt4-(4-Methoxy-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidineHCID 21979974—

Reaktionsbedingungen

Temperatur65 °C

Reaktionsschritte

A suspension of Intermediate 71 (600 mg) and copper(I) iodide (141 mg, Kanto Chemicals) in methanol (5.5 ml) and pyridine (5.5 ml) was added with sodium methoxide (28% methanol solution, 1.7 ml, Wako Pure Chemical Industries) and stirred with heating at 65° C. for 24 hours. The reaction mixture was cooled to room temperature, then added with water (30 ml) and extracted three times with ethyl acetate (20 ml for each time). The combined organic layer was washed twice with saturated brine (30 ml for each time) and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=1:2) to obtain the title compound (364 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07094789B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-e66b85a64f8c49938e94e99c298be080
Quellennotizuspto-grants-2006_08