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HRID 14487作成日:2026年10月24日

Water → 3-(4-Chlorophenyl)-2-isopropyl-7-(4-methoxybenzylamino)-8-nitro-chromen-4-one

https://huagongshe.com/ja/reaction/14487

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium CarbonateHCID 10340—
反応物4-Chlorophenylboronic acidHCID 74299—
反応物3-Bromo-2-isopropyl-7-(4-methoxybenzylamino)-8-nitro-chromen-4-oneHCID 68703155—
触媒Tetrakis(triphenylphosphine)palladiumHCID 11979704—
溶媒EthanolHCID 702—
生成物3-(4-Chlorophenyl)-2-isopropyl-7-(4-methoxybenzylamino)-8-nitro-chromen-4-oneHCID 68702877—

反応条件

温度100 °C

反応手順

3-Bromo-2-isopropyl-7-(4-methoxybenzylamino)-8-nitro-chromen-4-one (105 mg, 0.235 mmol), 4-chlorophenylboronic acid (73 mg, 0.47 mmol) and tetrakis(triphenylphosphine) palladium (0) (28 mg, 0.024 mmol) are dissolved in absolute ethanol (3 ml) in a 5 ml capacity microwave tube. Aqueous sodium carbonate solution (2M, 0.35 ml, 0.7 mmol) is added, and the mixture is heated at 100° C. under microwave irradiation for 10 min. The mixture is poured into water (10 ml) and extracted with ethyl acetate (3×30 ml). The ethyl acetate extracts are combined, washed with saturated brine (30 ml), dried (MgSO4), filtered and evaporated to give a green solid. This is triturated with n-pentane and filtered to give a pale yellow powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732435B2
出典データセットuspto-grants-2010_06
ORD IDord-aa5ee3cdfbea4142b6ea9b37f0e14d1e
出典メモuspto-grants-2010_06