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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1498838Erstellt: 27. Oktober 2026

Cerous carbonate → (S)-tert-butyl 2-((4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)methyl)morpholine-4-carboxylate

https://huagongshe.com/reaction/1498838

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCerous carbonateHCID 160516—
Edukt4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 2774010—
Edukt(S)-tert-butyl 2-((methylsulfonyloxy)methyl)morpholine-4-carboxylateHCID 86673567—
LösungsmittelAcetonitrileHCID 6342—
Produkt(S)-tert-butyl 2-((4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)methyl)morpholine-4-carboxylateHCID 12326214852,2%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

To a mixture of (S)-tert-butyl 2-((methylsulfonyloxy)methyl)morpholine-4-carboxylate (430 mg, 1.46 mmol) and 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (283 mg, 1.46 mmol) in 50 mL of acetonitrile was added cerium carbonate (1.43 g, 4.37 mmol), and the mixture was stirred at 60° C. for 3 h. TLC and LCMS showed the reaction was completed. After the solvents were removed under reduced pressure, the residue was diluted with 50 mL of ethyl acetate, and washed with water (50 mL×3) and brine. The organic layer was separated, dried over sodium sulfate, filtered and concentrated. The crude product was purified by silica gel chromatography (petroleum ether:ethyl acetate=5:1) to get the title product (300 mg, 52%) as colorless oil. MS (ES+) C19H32BN3O5 requires: 393. found: 394 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09200002B2
Quelldatensatzuspto-grants-2015_12
ORD IDord-e943a5067c014b4ba4e657bbf87c2da6
Quellennotizuspto-grants-2015_12