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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1839347Erstellt: 25. Oktober 2026

Ethyl Acetate → HCID 23387866, Verbindung

https://huagongshe.com/reaction/1839347

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
Edukt2-Methoxybenzoyloxymethyl chlorideHCID 23449271—
EduktSodium (1s,5r,6s)-6-((1r)-1-hydroxyethyl)-1-methyl-2-(7-methylthio-imidazo[5,1-b]thiazol-2-yl)-1-carbapen-2-em-3-carboxylateHCID 23669370—
KatalysatorBenzyl triethylammonium chlorideHCID 66133—
LösungsmittelDimethylformamideHCID 6228—
ProduktHCID 23387866HCID 23387866—

Reaktionsschritte

Sodium (1S,5R,6S)-6-((1R)-1-hydroxyethyl)-1-methyl-2-(7-methylthioimidazo[5,1-b]thiazol2-yl)-1-carbapen-2-em-3-carboxylate (170 mg) was dissolved in 2 ml of DMF. Triethylbenzylammonium chloride (193 mg) and 182 mg of 2-methoxybenzoyloxymethyl chloride were added to the solution in an argon atmosphere. The mixture was stirred under ice cooling for 2 hr and then stirred at room temperature for 5 hr. Ethyl acetate (30 ml) was added to the reaction solution. The mixture was washed twice with 20 ml of semisaturated brine. The organic layer was dried over anhydrous magnesium sulfate, filtered, and then concentrated to a volume of 5 ml under the reduced pressure. The residue was purified by column chromatography on silica gel (dichloromethane: methanol=40: 1) to give 131 mg of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06677331B2
Quelldatensatzuspto-grants-2004_01
ORD IDord-969dd61671a94d4e94269ab287b6d977
Quellennotizuspto-grants-2004_01