돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2073545생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/2073545

반응식

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 번호US04918094
출처 데이터셋uspto-grants-1990_04
ORD IDord-ab9345e05c5441c6b5bd0c7509b0dd0c
출처 메모uspto-grants-1990_04