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HRID 728675作成日:2026年10月25日

Acrylamide → 1-(2-carbamoylethyl)-5-(N-cyclopentylmethylcarbamoyl)indole

https://huagongshe.com/reaction/728675

反応式

関与物質

役割名称HCID仕込み量
反応物AcrylamideHCID 6579—
反応物Sodium hydrideHCID 24758—
反応物Ammonium ChlorideHCID 25517—
反応物1h-Indole-5-carboxamide,n-(cyclopentylmethyl)-HCID 10037396—
溶媒DimethylformamideHCID 6228—
生成物1-(2-carbamoylethyl)-5-(N-cyclopentylmethylcarbamoyl)indoleHCID 1982247736.1%

反応条件

温度0 °C

反応手順

A solution of 5-(N-cyclopentylmethylcarbamoyl)indole (A)(1.50 g) in N,N-dimethylformamide (DMF) (5 ml) was added to a stirred slurry of sodium hydride (0.16 g) in DMF (15 ml) maintained at 0° C. under an atmosphere of nitrogen. The mixture was warmed to room temperature for 15 minutes, treated with a solution of acrylamide (0.66 g) in DMF (5 ml), and allowed to stir for 12 hours. The mixture was poured into a cold, saturated aqueous solution of ammonium chloride to give a milky suspension which was extracted with ethyl acetate. The organic phase was washed successively with water and brine, dried (MgSO4), and evaporated. The resulting clear oil was purified by flash chromatography on silica gel (700 ml), eluting with 7:93 v/v methanol:ethyl acetate, to give 1-(2-carbamoylethyl)-5-(N-cyclopentylmethylcarbamoyl)indole (0.70 g, 36%) as a gummy white foam; NMR (80 MHz, CDCl3): 1.2-2.2(broad m, 9H, cyclopentyl), 2.7(t, 2H, CH2CO), 3.4 (dd, 2H, CH2NH), 4.5(t, 2H, CH2CH2CO), 5.4(broad, 2H, CONH2), 6.5(dd, 1H, H3 -indole), 7.2(d, 1H, H2 -indole), 7.3(d, 1H, H7 -indole), 7.6(dd, 1H, H6 -indole), 8.0(m, 1H, H4 -indole).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05049679
出典データセットuspto-grants-1991_09
ORD IDord-8b05121848f94a8bba8f79c029c9c427
出典メモuspto-grants-1991_09