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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 727941Erstellt: 25. Oktober 2026

Ethyl Acetate → 1-(2,4-Difluorophenyl)-6-fluoro-1,4-dihydro7-(5((5-methyl-2-oxo-1,3-dioxolen-4-yl)methyl)-2,5diazabicyclo(2.2.1)-hept-2-yl)-4-oxoquinoline-3-carboxylic acid

https://huagongshe.com/reaction/727941

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktCalcium bicarbonateHCID 10176262—
Edukt4-(Bromomethyl)-5-methyl-1,3-dioxol-2-oneHCID 10774141—
Edukt7-(2,5-Diazabicyclo(2.2.1)hept-2-yl)-6-fluoro-1-(2,4-difluorophenyl)-1,4-di-hydro-4-oxoquinoline-3-carboxylic acid monohydrateHCID 67927890—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-(2,4-Difluorophenyl)-6-fluoro-1,4-dihydro7-(5((5-methyl-2-oxo-1,3-dioxolen-4-yl)methyl)-2,5diazabicyclo(2.2.1)-hept-2-yl)-4-oxoquinoline-3-carboxylic acidHCID 1401483527,5%

Reaktionsschritte

To 188 mg (0.434 m Mol) of 7-(2,5-diazabicyclo(2.2.1)hept-2-yl)-6-fluoro-1-(2,4-difluorophenyl)-1,4-di-hydro-4-oxoquinoline-3-carboxylic acid monohydrate (Example 11) was suspended in 20 ml dry DMF was added 96 mg (0.95 m Mol) anhydrous calcium bicarbonate and 92 mg (0.48 m Mol) 4-bromomethyl-5-methyl-1,3-dioxolen-2-one. The resultant suspension was stirred at room temperature for 10 hrs. Then the suspension was treated with 150 ml of ethyl acetate and 50 ml of water. The organic phase was separated and washed with 5×30 ml water, dried over sodium sulfate, filtered the volatiles were removed at room temperature under reduced pressure. Recrystallization from ethyl acetate gave 63 mg (27.5%) of the desired material.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05045549
Quelldatensatzuspto-grants-1991_09
ORD IDord-91c076c09db74192bcdea3de1c3ea8e2
Quellennotizuspto-grants-1991_09