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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 493609Erstellt: 25. Oktober 2026

Acetic Acid → Ethyl 4-[({3-[(tert-butoxycarbonyl)amino]pyridin-4-yl}methyl)amino]piperidine-1-carboxylate

https://huagongshe.com/reaction/493609

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
Edukt1,1-DichloroethaneHCID 6365—
EduktEthyl 4-amino-1-piperidinecarboxylateHCID 100867—
EduktSodium triacetoxyborohydrideHCID 5049666—
EduktN-Boc-3-amino-4-pyridine carboxaldehydeHCID 70700445—
ProduktEthyl 4-[({3-[(tert-butoxycarbonyl)amino]pyridin-4-yl}methyl)amino]piperidine-1-carboxylateHCID 22293284—

Reaktionsschritte

Sodium triacetoxyborohydride (0.57 g, 2.70 mmol) and acetic acid (0.41, 6.75 mmol) were added to a solution of N-Boc-3-amino-4-pyridine carboxaldehyde (0.50 g, 2.25 mmol) and ethyl 4-aminopiperidine-1-carboxylate (0.47 g, 2.70 mmol) in dichloroethane (5 mL) at room temperature. The reaction was stirred overnight, and quenched with saturated aqueous sodium bicarbonate. This was separated, extracted with ethyl acetate and the combined organics were dried over sodium sulfate. The solution was filtered and evaporated to give the crude product. This was purified by chromatography (silica gel, 1 to 12% methanol in methylene chloride gradient elution), which gave the title compound (0.47 g). MS 379.3.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07534784B2
Quelldatensatzuspto-grants-2009_05
ORD IDord-f2e61167496649fd8a22016ac6a7bf06
Quellennotizuspto-grants-2009_05