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HRID 402845作成日:2026年10月25日

Potassium Carbonate → 4-cyclopropyl-1-isopropyl-1H-indole-3-carbaldehyde

https://huagongshe.com/reaction/402845

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Cyclopropylboronic acidHCID 2760897—
反応物4-bromo-1-isopropyl-1H-indole-3-carbaldehydeHCID 77230881—
触媒HCID 178454869HCID 178454869—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物4-cyclopropyl-1-isopropyl-1H-indole-3-carbaldehydeHCID 7723087718.5%

反応条件

温度140 °C

反応手順

To a solution of 4-romo-1-(propan-2-yl)-1H-indole-3-carboxaldehyde (120 mg, 0.451 mmol) (from Example 9-1, Step 1) and cyclopropylboronic acid (77 mg, 0.902 mmol) in dioxane (2 mL) and water (0.5 mL) in a 5 mL microwave reaction vial was added potassium carbonate (187 mg, 1.35 mmol) and dichloro[1,1′-bis(di-t-butylphosphino)ferrocene]palladium (II) (29 mg, 0.045 mmol). The reaction was placed under nitrogen, sealed and heated in a microwave reactor at 140° C. for 25 minutes. The solvent was removed in vacuo and the residue was partitioned with ethyl acetate and aqueous sodium bicarbonate and extracted twice with ethyl acetate. The organic layers were washed with brine, dried over sodium sulfate, filtered and concentrated. The residue was purified on silica gel (COMBI FLASH 24 gm column, gradient of 0-100% ethyl acetate/hexanes) to give the title intermediate (19 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08742110B2
出典データセットuspto-grants-2014_06
ORD IDord-c464cef29b1846db90279fe2d76f9849
出典メモuspto-grants-2014_06