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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 728597생성일: 2026년 10월 27일

1H-Indole-5-Carboxylic Acid → 1h-Indole-5-carboxamide,n-(cyclopentylmethyl)-

https://huagongshe.com/reaction/728597

반응식

참여 물질

역할이름HCID투입량
반응물1H-Indole-5-Carboxylic AcidHCID 74280—
반응물CyclopentanemethylamineHCID 80153—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
생성물1h-Indole-5-carboxamide,n-(cyclopentylmethyl)-HCID 1003739680%

반응 단계

A solution of cyclopentylmethylamine (2.66 g), 5-carboxyindole (4.76 g), 4-(dimethylamino)pyridine (3.60 g) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (5.67 g) in dichloromethane (60 ml) was stirred for 12 hours under an atmosphere of nitrogen. The amber solution was diluted with dichloromethane (150 ml), washed successively with 10% (w/v) aqueous sodium carbonate, 10% (v/v) hydrochloric acid, water, and brine, dried (MgSO4), and evaporated. The residual amber oil was purified by flash chromatography on silica gel (700 ml), eluting with 1:3 v/v ethyl acetate:chloroform, to yield 5-(N-cyclopentylmethylcarbamoyl)indole (A) (5.17 g, 80%) as a white crystalline solid; mp 110°-112° C.; NMR (80 MHz, CDCl3): 1.0-2.4(broad m, 9H, cyclopentyl), 3.4(dd, 2H, CH2N), 6.2(broad, 1H, NH), 6.6(m, 1H, H3 -indole), 7.3(t, 1H, H2 -indole), 7.4(d, 1H, H7 -indole), 8.5(broad, 1H, CONH).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05049576
출처 데이터셋uspto-grants-1991_09
ORD IDord-d06b1ddac7024f6fb51234454273df9c
출처 메모uspto-grants-1991_09