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HRID 1084846作成日:2026年10月27日

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

https://huagongshe.com/reaction/1084846

反応式

関与物質

役割名称HCID仕込み量
反応物BromoacetateHCID 6226—
反応物DimethylformamideHCID 6228—
反応物Potassium CarbonateHCID 11430—
反応物3-(4-fluorophenyl)-1-(3-hydroxyphenyl)-1H-pyrazolo[3,4-b]pyridineHCID 14796258—
生成物ethyl 3-[3-(4-fluorophenyl)-1H-pyrazolo[3,4-b]pyridin-1-yl]phenoxyacetateHCID 14796397—

反応条件

温度65 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05006520
出典データセットuspto-grants-1991_04
ORD IDord-9164fce7ed04476483c591b2ab31585e
出典メモuspto-grants-1991_04