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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 278196Erstellt: 24. Oktober 2026

Hydrazine, ethyl-, ethanedioate (1:1) → 4-(5-benzyl-1-ethyl-(1H-pyrazol-3-yl))-1-t-butoxycarbonylpiperidine

https://huagongshe.com/de/reaction/278196

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrazine, ethyl-, ethanedioate (1:1)HCID 96181—
EduktTert-butyl 4-(3-oxo-4-phenylbutanoyl)piperidine-1-carboxylateHCID 18187492—
LösungsmittelMethanolHCID 887—
Produkt4-(5-benzyl-1-ethyl-(1H-pyrazol-3-yl))-1-t-butoxycarbonylpiperidineHCID 18187572—

Reaktionsschritte

1-(1-(t-Butoxycarbonyl)piperidin-4-yl)-4-phenylbutane-1,3-dione from Step A, from Method A or Method B, Step B3, (0.851 g, 2.46 mmol) in methanol (25 mL) was added over 10 min to a suspension of ethylhydrazine oxalate (0.444 g, 2.96 mmol) in methanol (5 mL) in a 60° C. oil bath. After 15 h, the reaction was concentrated in vacuo and the residue was purified by repeated FC using a gradient of 50-100% ethyl acetate in hexanes to give first 4-(5-benzyl-1-ethyl-(1H)-pyrazol-3-yl)-1-(t-butoxycarbonyl)piperidine (0.148 g total) as the higher Rf product isomer and then the title compound (0.373 g total) as the lower Rf.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06358979B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-aed7462254044a879c7c6e67b28059ee
Quellennotizuspto-grants-2002_03