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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1084846Erstellt: 26. Oktober 2026

Bromoacetate → ethyl 3-[3-(4-fluorophenyl)-1H-pyrazolo[3,4-b]pyridin-1-yl]phenoxyacetate

https://huagongshe.com/reaction/1084846

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBromoacetateHCID 6226—
EduktDimethylformamideHCID 6228—
EduktPotassium CarbonateHCID 11430—
Edukt3-(4-fluorophenyl)-1-(3-hydroxyphenyl)-1H-pyrazolo[3,4-b]pyridineHCID 14796258—
Produktethyl 3-[3-(4-fluorophenyl)-1H-pyrazolo[3,4-b]pyridin-1-yl]phenoxyacetateHCID 14796397—

Reaktionsbedingungen

Temperatur65 °C

Reaktionsschritte

In 200 ml of dimethylformamide were suspended 20 g of 3-(4-fluorophenyl)-1-(3-hydroxyphenyl)-1H-pyrazolo[3,4-b]pyridine, 21.9 g of bromoacetate and 18.1 g of potassium carbonate. The mixture was stirred at 65° C. for 4 hours. The reaction mixture was concentrated under reduced pressure. The residue was extracted with ethyl acetate-water. The organic layer was concentrated. Hexane was added to the residue for crystallization. The obtained crude crystals were recrystallized from isopropyl ether to give 10.9 g of ethyl 3-[3-(4-fluorophenyl)-1H-pyrazolo[3,4-b]pyridin-1-yl]phenoxyacetate, m.p. 130°-131° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05006520
Quelldatensatzuspto-grants-1991_04
ORD IDord-9164fce7ed04476483c591b2ab31585e
Quellennotizuspto-grants-1991_04