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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 501095Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/501095

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
Edukt1,1-DichloroethaneHCID 6365—
EduktEthyl 4-amino-1-piperidinecarboxylateHCID 100867—
EduktSodium triacetoxyborohydrideHCID 5049666—
EduktN-Boc4-amino-3-pyridine carboxaldehydeHCID 20848820—
ProduktEthyl 4-[(4-[(tert-butoxycarbonyl)amino]pyridin-3-yl methyl)amino]piperidine-1-carboxylateHCID 22293255—

Reaktionsschritte

Sodium triacetoxyborohydride (1.70 g, 8.03 mmol) and acetic acid (0.29, 4.82 mmol) were added to a solution of N-Boc-4-amino-3-pyridine carboxaldehyde (0.36 g, 1.61 mmol) and ethyl 4-aminopiperidine-1-carboxylate (0.33 g, 1.93 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, 0 to 12% methanol in methylene chloride gradient elution), which gave the title compound (0.24 g). MS 379.2.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07772224B2
Quelldatensatzuspto-grants-2010_08
ORD IDord-3f40b43b978244a59033fcc07427658f
Quellennotizuspto-grants-2010_08