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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 728675생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/728675

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참여 물질

역할이름HCID투입량
반응물AcrylamideHCID 6579—
반응물Sodium hydrideHCID 24758—
반응물Ammonium ChlorideHCID 25517—
반응물1h-Indole-5-carboxamide,n-(cyclopentylmethyl)-HCID 10037396—
용매DimethylformamideHCID 6228—
생성물1-(2-carbamoylethyl)-5-(N-cyclopentylmethylcarbamoyl)indoleHCID 1982247736.1%

반응 조건

온도0 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05049679
출처 데이터셋uspto-grants-1991_09
ORD IDord-8b05121848f94a8bba8f79c029c9c427
출처 메모uspto-grants-1991_09