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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 256315Erstellt: 25. Oktober 2026

Ciprofloxacin → 1-Cyclopropyl-6-fluoro-1,4-dihydro-7-[4-(5-methyl-2-oxo-1,3-dioxol-4-yl-methyl)-1-piperazinyl]-4-oxo-3-quinolinecarboxylic acid

https://huagongshe.com/reaction/256315

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCiprofloxacinHCID 2764—
EduktPotassium BicarbonateHCID 516893—
Edukt4-(Bromomethyl)-5-methyl-1,3-dioxol-2-oneHCID 10774141—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-Cyclopropyl-6-fluoro-1,4-dihydro-7-[4-(5-methyl-2-oxo-1,3-dioxol-4-yl-methyl)-1-piperazinyl]-4-oxo-3-quinolinecarboxylic acidHCID 13673272—

Reaktionsschritte

1.15 g (3.5 mmoles) of 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinolinecarboxylic acid are stirred in 20 ml of dimethylformamide with 0.85 g (4.4 mmoles) of 4-bromomethyl-5-methyl-1,3-dioxol-2-one and 0.42 g (4.2 mmoles) of powdered potassium bicarbonate for 3 days, while cooling with ice. The mixture is concentrated in vacuo, the residue is stirred with 20 ml of water, the resulting greasy product is dissolved in methanol and the solution is filtered. The filtrate is left to stand at room temperature for 2 days and the colorless crystals which have precipitated are isolated.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04703047
Quelldatensatzuspto-grants-1987_10
ORD IDord-a73071cede0544c8b4b53d87ab259d7d
Quellennotizuspto-grants-1987_10