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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1072635Erstellt: 25. Oktober 2026

Cyclohexene → HCID 178418962, Verbindung

https://huagongshe.com/reaction/1072635

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCyclohexeneHCID 8079—
Edukt2-acetylamino-N-[2-[2-(1-benzyl-1H-imidazol-4-ylmethyl)-5-naphthalen-2-ylmethyl-3-oxo-piperazin-1-yl]-1-(4-fluorobenzyl)-2-oxo-ethyl]-3-(4-hydroxyphenyl)-propionamideHCID 69652750—
KatalysatorPalladiumHCID 23938—
LösungsmittelAcetic acid ethanolHCID 18476134—
ProduktHCID 178418962HCID 178418962—

Reaktionsschritte

2-acetylamino-N-[2-[2-(1-benzyl -1H-imidazol-4-ylmethyl)-5-naphthalen-2-ylmehtyl-3-oxo-piperazin-1-yl]-1-(4-fluorobenzyl)-2-oxo-ethyl]-3-(4-hydroxyphenyl)-propionamide, 73, (0.22 g, 0.28 mmol) is dissolved in ethanol/acetic acid (4:1) (3 mL). Cyclohexene (3 mL) and Pd-black are added and the solution is refluxed with periodic replenishment of cyclohexene. The reaction is monitored by TLC and after 2 days is cooled and filtered through Celite to remove the catalyst. The filtrate is concentrated in vacuo to afford an oil which is purified by reverse phase C18 prep HPLC to afford the desired product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06911447B2
Quelldatensatzuspto-grants-2005_06
ORD IDord-532e90c5df73486aa3183da0c661bf5d
Quellennotizuspto-grants-2005_06