Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1502002Erstellt: 24. Oktober 2026

tert-butyl (3S)-3-(hydroxymethyl)piperazine-1-carboxylate → (3S)-tert-butyl 4-(2-(3-cyano-4-fluoro-2-methylphenyl)-2-hydroxyethyl)-3-(hydroxymethyl)piperazine-1-carboxylate

https://huagongshe.com/de/reaction/1502002

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukttert-butyl (3S)-3-(hydroxymethyl)piperazine-1-carboxylateHCID 24820294—
Edukt6-Fluoro-2-methyl-3-(oxiran-2-yl)benzonitrileHCID 86647307—
LösungsmittelEthanolHCID 702—
Produkt(3S)-tert-butyl 4-(2-(3-cyano-4-fluoro-2-methylphenyl)-2-hydroxyethyl)-3-(hydroxymethyl)piperazine-1-carboxylateHCID 71272768—

Reaktionsbedingungen

Temperatur150 °C

Reaktionsschritte

A mixture of 6-fluoro-2-methyl-3-(oxiran-2-yl)benzonitrile (785 mg, 4.43 mmol) and (S)-tert-butyl 3-(hydroxymethyl)piperazine-1-carboxylate (1340 mg, 6.2 mmol) in ethanol (10 mL) was heated in microwave at 150° C. for 3 h. The volatile was evaporated and the residue was purified on Biotage using 40-100% ethyl acetate/hexane to give the title compound: LC/MS: (M+1)+: 394.19.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09206199B2
Quelldatensatzuspto-grants-2015_12
ORD IDord-2f311955a74b4d2398d0f33b26a934d0
Quellennotizuspto-grants-2015_12