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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2109849Erstellt: 26. Oktober 2026

Diethyl Oxalate → HCID 54705274, Verbindung

https://huagongshe.com/reaction/2109849

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl OxalateHCID 7268—
EduktTetrahydrofuranHCID 8028—
EduktSodium bis(trimethylsilyl)amideHCID 2724254—
Edukt4-Acetyl-5-[(1,1-Dioxido-1,2-thiazinan-2-yl)methyl]-1-(4-fluorobenzyl)-piperazin-2-oneHCID 57634651—
LösungsmittelDimethylformamideHCID 6228—
ProduktHCID 54705274HCID 54705274—

Reaktionsschritte

To a cold (0° C.) solution of 4-acetyl-5-[(1,1-dioxido-1,2-thiazinan-2-yl)methyl]-1-(4-fluorobenzyl)-piperazin-2-one (75 mg, 0.19 mmol) and diethyl oxalate (29 μL, 0.21 mmol) in DMF (3 mL) under an atmosphere of nitrogen, a solution of sodium bis(trimethylsilyl)amide in THF (1M, 0.21 mL, 0.21 mmol) was added over a period of 0.5 h and stirred at the temperature for 30 min. Then additional sodium bis(trimethylsilyl)amide in THF (1M, 0.21 mL, 0.21 mmol) was added over a period of 0.5 h and stirred at the temperature for 1 h. The product mixture was concentrated under vacuum, and the residue partitioned between aqueous HCl and ethyl acetate. The organic extract was dried over anhydrous magnesium sulfate, filtered, and concentrated under vacuum. The residue was subjected to HPLC purification on C-18 stationary phase eluted with water/acetonitrile/TFA mobile phase. Collection and lyophilization of appropriate fractions provided the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07517532B2
Quelldatensatzuspto-grants-2009_04
ORD IDord-fb74c6886a72467d887c50102143032b
Quellennotizuspto-grants-2009_04