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HRID 729797作成日:2026年10月25日

Sodium Bicarbonate → (3-(1H-pyrrolo[2,3-b]pyridin-5-yl)phenyl)(morpholino)methanone

https://huagongshe.com/reaction/729797

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium BicarbonateHCID 516892—
反応物3-(Morpholine-4-carbonyl)phenylboronic acidHCID 3602916—
反応物5-bromo-1H-pyrrolo[2,3-b]pyridineHCID 10307932—
触媒HCID 178418397HCID 178418397—
溶媒1,4-Dioxane--water (1/1)HCID 21886435—
生成物(3-(1H-pyrrolo[2,3-b]pyridin-5-yl)phenyl)(morpholino)methanoneHCID 4983076784%

反応条件

温度110 °C

反応手順

A mixture of 5-bromo-1H-pyrrolo[2,3-b]pyridine(3 g, 15 mmol), 3-(morpholine-4-carbonyl)phenylboronic acid (4 g, 18 mmol), sodium bicarbonate (4 g, 46 mmol), and tetrakis(triphenylphosphine)palladium(0) in dioxane/water (100 mL/20 mL) was stirred at 110° C. for 15 hours. The mixture was then poured into ice water and extracted with ethyl acetate (3×). The organic layers were combined, dried over sodium sulfate, filtered and concentrated to dryness. Silica gel chromatography of the crude product afforded (3-(1H-pyrrolo[2,3-b]pyridin-5-yl)phenyl)(morpholino)methanone (3.86 g, 84% yield) as yellow solids. MS: m/z 308.1 (M+H+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07582637B2
出典データセットuspto-grants-2009_09
ORD IDord-8088b661ca6648149508a8762c7732f1
出典メモuspto-grants-2009_09