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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 20975Erstellt: 23. Oktober 2026

Acetic Acid → 5-[4-(Tert-butoxycarbonyl)piperazin-1-ylmethyl]indole

https://huagongshe.com/de/reaction/20975

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktSodium CarbonateHCID 10340—
Edukttert-Butyl piperazine-1-carboxylateHCID 143452—
EduktIndole-5-carboxaldehydeHCID 589040—
EduktSodium triacetoxyborohydrideHCID 5049666—
LösungsmittelWaterHCID 962—
LösungsmittelAcetonitrileHCID 6342—
Produkt5-[4-(Tert-butoxycarbonyl)piperazin-1-ylmethyl]indoleHCID 6848993447%

Reaktionsschritte

5-Formylindole (500 mg, 3.44 mmol) was dissolved in acetonitrile (10 mL), and the solution was added with 1-(tert-butoxycarbonyl)piperazine (961 mg, 5.16 mmol), acetic acid (3.90 mL, 68.1 mmol) and sodium triacetoxyborohydride (3.65 g, 17.2 mmol) little by little, followed by stirring at room temperature for 2 hours. The reaction mixture was added with water and sodium carbonate to adjust the pH to 9, followed by extracting with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by flash column chromatography (hexane/ethyl acetate=19/1, 7/3, 1/1) to obtain 5-[4-(tert-butoxycarbonyl)piperazin-1-ylmethyl]indole (505 mg, yield 47%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745641B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-40825bde11ad4d73a783930ebca6be83
Quellennotizuspto-grants-2010_06