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HRID 252548作成日:2026年10月25日

Chloroacetyl isocyanate → 2-[4-(2,4-dioxo-imidazolidin-1-yl)phenyl]-6-ethoxy-1-ethyl-1H-indole-3-carbonitrile

https://huagongshe.com/reaction/252548

反応式

関与物質

役割名称HCID仕込み量
反応物Chloroacetyl isocyanateHCID 78209—
反応物1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
反応物2-(4-aminophenyl)-6-ethoxy-1-ethyl-1H-indole-3-carbonitrileHCID 59425274—
溶媒1,4-DioxaneHCID 31275—
生成物2-[4-(2,4-dioxo-imidazolidin-1-yl)phenyl]-6-ethoxy-1-ethyl-1H-indole-3-carbonitrileHCID 5942494579%

反応条件

温度60 °C

反応手順

A solution of 2-(4-aminophenyl)-6-ethoxy-1-ethyl-1H-indole-3-carbonitrile (319 mg, 1.04 mmol) in 1,4-dioxane (3 mL) is treated with chloroacetyl isocyanate (0.10 mL, 1.17 mmol), and the resulting solution is warmed to 60° C. overnight. The solution is cooled, and DBU (0.20 mL, 1.31 mmol) is added. This mixture is stirred at ambient temperature overnight, and then is partitioned between water and ethyl acetate (50 mL each). The organic layer is washed with saturated brine, and then dried over anhydrous magnesium sulfate, filtered and evaporated. The residual material is triturated with ether, and the resulting solid is collected by filtration and dried under high vacuum to afford the title product (319 mg, 0.821 mmol, 79%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07868037B2
出典データセットuspto-grants-2011_01
ORD IDord-b7abacf659a847fbafaf41713fa7b860
出典メモuspto-grants-2011_01