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HRID 1935215作成日:2026年10月27日

Sodium Carbonate → 3-cyclopentyl-2-[4-(1H-indol-5-yl)-phenyl]-propionic acid methyl ester

https://huagongshe.com/reaction/1935215

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物5-Indolylboronic acidHCID 2734361—
反応物3-Cyclopentyl-2-(4-iodo-phenyl)-propionic acid methyl esterHCID 67483447—
触媒HCID 178418476HCID 178418476—
溶媒WaterHCID 962—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物3-cyclopentyl-2-[4-(1H-indol-5-yl)-phenyl]-propionic acid methyl esterHCID 6748521836%

反応条件

温度25 °C

反応手順

A slurry of dichlorobis(triphenylphosphine)palladium(II) (119 mg, 0.17 mmol) in 1,2-dimethoxyethane (10 mL) was treated with 3-cyclopentyl-2-(4-iodo-phenyl)-propionic acid methyl ester (1.00 g, 2.79 mmol). The reaction slurry was stirred at 25° C. for 10 min and then treated with a mixture of 5-indolylboronic acid (670 mg, 4.19 mmol) in water (5 mL) and a 2M aqueous sodium carbonate solution (2.8 mL, 5.58 mmol). The resulting reaction mixture was heated under reflux for 2 h. The reaction mixture was allowed to cool to 25° C. and then filtered to remove the catalyst. The filtrate was partitioned between water (50 mL) and methylene chloride (50 mL), and the layers were separated. The aqueous layer was further extracted with methylene chloride (50 mL). The combined organic extracts were dried over magnesium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 1/2 hexanes/ethyl acetate) afforded 3-cyclopentyl-2-[4-(1H-indol-5-yl)-phenyl]-propionic acid methyl ester (347 mg, 36%) as a light brown oil: EI-HRMS m/e calcd for C23H25NO2 (M+) 347.1885, found 347.1887.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06384220B2
出典データセットuspto-grants-2002_05
ORD IDord-48c9ed735f6d4f15944f3d4db57ce520
出典メモuspto-grants-2002_05