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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 522629Erstellt: 25. Oktober 2026

Cesium carbonate → (S)-tert-butyl 2-((4-nitro-1H-pyrazol-1-yl)methyl)morpholine-4-carboxylate

https://huagongshe.com/reaction/522629

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCesium carbonateHCID 10796—
Edukt4-nitro-1H-pyrazoleHCID 16376—
Edukt(S)-tert-butyl 2-((methylsulfonyloxy)methyl)morpholine-4-carboxylateHCID 86673567—
LösungsmittelAcetonitrileHCID 6342—
Produkt(S)-tert-butyl 2-((4-nitro-1H-pyrazol-1-yl)methyl)morpholine-4-carboxylateHCID 118023401107,7%

Reaktionsbedingungen

Temperatur55 °C

Reaktionsschritte

To a solution of (S)-tert-butyl 2-((methylsulfonyloxy)methyl)morpholine-4-carboxylate (2.8 g, 9.5 mmol) and 4-nitro-1H-pyrazole (715 mg, 6.3 mmol) in acetonitrile (100 mL) was added cesium carbonate (6.2 g, 19.0 mmol). The reaction mixture was stirred at 55° C. overnight and then concentrated. The residue was dissolved in ethyl acetate (100 mL), washed with water (50 mL), dried over sodium sulfate, filtered and concentrated. The crude sample was purified by silica gel chromatography, eluting with petroleum ether:ethyl acetate=8:1, to afford (S)-tert-butyl 2-((4-nitro-1H-pyrazol-1-yl)methyl)morpholine-4-carboxylate as a yellow oil (2.12 g, 71%). MS (ES+) C13H20N4O5 requires: 312, found: 257 [M+H-56]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09334263B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-569ae0dfd35e4a7a8fd5e1dd96f9ab2f
Quellennotizuspto-grants-2016_05